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
109743303 10974330 3 F 2006 20160708 20150401 20160711 EXP US-009507513-1503USA015130 MERCK 0.00 M Y 0.00000 20160711 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
109743303 10974330 1 PS PROPECIA FINASTERIDE 1 Oral 1 MG, QD N 20788 1 MG FILM-COATED TABLET QD
109743303 10974330 2 SS PROPECIA FINASTERIDE 1 Oral 1 MG, UNKNOWN N 20788 1 MG FILM-COATED TABLET
109743303 10974330 3 SS FINASTERIDE. FINASTERIDE 1 Oral 1 MG, QD N 20788 1 MG FILM-COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109743303 10974330 1 Androgenetic alopecia
109743303 10974330 2 Alopecia
109743303 10974330 3 Androgenetic alopecia

Outcome of event

Event ID CASEID OUTC COD
109743303 10974330 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
109743303 10974330 Cognitive disorder
109743303 10974330 Dyslipidaemia
109743303 10974330 Erectile dysfunction
109743303 10974330 Gynaecomastia
109743303 10974330 Hydrocele
109743303 10974330 Impaired fasting glucose
109743303 10974330 Loss of libido
109743303 10974330 Pharyngitis
109743303 10974330 Seasonal allergy
109743303 10974330 Sexual dysfunction
109743303 10974330 Sinusitis
109743303 10974330 Testicular pain
109743303 10974330 Upper respiratory tract infection

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
109743303 10974330 1 200505 200803 0
109743303 10974330 2 200803 201203 0
109743303 10974330 3 20130424 0