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
110457384 11045738 4 F 1998 20160712 20150417 20160714 EXP US-009507513-1504USA017077 MERCK 0.00 M Y 89.80000 KG 20160714 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
110457384 11045738 1 PS PROPECIA FINASTERIDE 1 Oral UNK 20788 FILM-COATED TABLET
110457384 11045738 2 SS PROSCAR FINASTERIDE 1 Oral 5 MG, UNK 0 5 MG FILM-COATED TABLET
110457384 11045738 3 SS FINASTERIDE. FINASTERIDE 1 Oral 5 MG, UNK 0 5 MG FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
110457384 11045738 1 Alopecia
110457384 11045738 2 Alopecia
110457384 11045738 3 Alopecia

Outcome of event

Event ID CASEID OUTC COD
110457384 11045738 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
110457384 11045738 Anxiety
110457384 11045738 Depressed mood
110457384 11045738 Depression
110457384 11045738 Drug administration error
110457384 11045738 Emotional distress
110457384 11045738 Erectile dysfunction
110457384 11045738 Sexual dysfunction
110457384 11045738 Type V hyperlipidaemia

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
110457384 11045738 1 1998 2006 0
110457384 11045738 2 2006 0
110457384 11045738 3 2003 2006 0