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
110312603 11031260 3 F 2009 20160812 20150415 20160819 EXP US-009507513-1504USA012366 MERCK 0.00 M Y 0.00000 20160819 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
110312603 11031260 1 PS 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
110312603 11031260 1 Alopecia

Outcome of event

Event ID CASEID OUTC COD
110312603 11031260 OT
110312603 11031260 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
110312603 11031260 Brain injury
110312603 11031260 Depression
110312603 11031260 Ejaculation disorder
110312603 11031260 Endocrine disorder
110312603 11031260 Erectile dysfunction
110312603 11031260 Hormone level abnormal
110312603 11031260 Loss of libido
110312603 11031260 Painful ejaculation
110312603 11031260 Penile size reduced
110312603 11031260 Penis injury
110312603 11031260 Sexual dysfunction
110312603 11031260 Sleep apnoea syndrome
110312603 11031260 Testicular disorder

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
110312603 11031260 1 20090717 2011 0