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
92472745 9247274 5 F 20041005 20160711 20130423 20160713 PER US-009507513-1304USA007695 MERCK 0.00 M Y 0.00000 20160713 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
92472745 9247274 1 PS PROPECIA FINASTERIDE 1 Oral 1 MG, UNK U 20788 1 MG FILM-COATED TABLET
92472745 9247274 2 SS PROSCAR FINASTERIDE 1 Oral 1.25 MG, UNK U 0 1.25 MG FILM-COATED TABLET
92472745 9247274 3 SS FINASTERIDE. FINASTERIDE 1 Oral 1.25 MG, UNK U 0 1.25 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
92472745 9247274 1 Alopecia
92472745 9247274 2 Alopecia
92472745 9247274 3 Alopecia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
92472745 9247274 Abdominal discomfort
92472745 9247274 Cognitive disorder
92472745 9247274 Drug administration error
92472745 9247274 Erectile dysfunction
92472745 9247274 Influenza
92472745 9247274 Loss of libido
92472745 9247274 Sexual dysfunction
92472745 9247274 Wrong technique in product usage process

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
92472745 9247274 1 20040921 200503 0
92472745 9247274 2 20041005 20041217 0
92472745 9247274 3 20070404 0