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
92396356 9239635 6 F 2007 20160711 20130418 20160712 PER US-009507513-1304USA008274 MERCK 0.00 M Y 0.00000 20160712 PH 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
92396356 9239635 1 PS PROPECIA FINASTERIDE 1 Oral 1 MG, QD 20788 1 MG FILM-COATED TABLET QD
92396356 9239635 2 SS PROPECIA FINASTERIDE 1 Oral 1 MG, QD 20788 1 MG FILM-COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
92396356 9239635 1 Androgenetic alopecia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
92396356 9239635 Amnesia
92396356 9239635 Anxiety
92396356 9239635 Asthma
92396356 9239635 Bladder neck obstruction
92396356 9239635 Depression
92396356 9239635 Disorientation
92396356 9239635 Erectile dysfunction
92396356 9239635 Fatigue
92396356 9239635 Lower urinary tract symptoms
92396356 9239635 Pollakiuria
92396356 9239635 Prostatitis
92396356 9239635 Seborrhoeic dermatitis
92396356 9239635 Sexual dysfunction
92396356 9239635 Sexual relationship change
92396356 9239635 Weight increased

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
92396356 9239635 1 20070703 20081217 0
92396356 9239635 2 2009 20120316 0