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
110388265 11038826 5 F 2003 20160630 20150416 20160701 EXP US-009507513-1504USA013053 MERCK 0.00 M Y 79.37000 KG 20160701 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
110388265 11038826 1 PS PROPECIA FINASTERIDE 1 Oral 1 MG, QD U 20788 1 MG FILM-COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
110388265 11038826 1 Alopecia

Outcome of event

Event ID CASEID OUTC COD
110388265 11038826 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
110388265 11038826 Blood creatinine increased
110388265 11038826 Brain injury
110388265 11038826 Breast disorder
110388265 11038826 Depression
110388265 11038826 Ejaculation disorder
110388265 11038826 Endocrine disorder
110388265 11038826 Erectile dysfunction
110388265 11038826 Hormone level abnormal
110388265 11038826 Hypertension
110388265 11038826 Intraductal papillary breast neoplasm
110388265 11038826 Intraductal proliferative breast lesion
110388265 11038826 Loss of libido
110388265 11038826 Painful ejaculation
110388265 11038826 Penile size reduced
110388265 11038826 Penis injury
110388265 11038826 Seborrhoeic keratosis
110388265 11038826 Sexual dysfunction
110388265 11038826 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
110388265 11038826 1 2003 2007 0