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
92492246 9249224 6 F 2003 20160912 20130423 20160915 EXP US-009507513-1304USA011000 MERCK 0.00 M Y 0.00000 20160915 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
92492246 9249224 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
92492246 9249224 1 Androgenetic alopecia

Outcome of event

Event ID CASEID OUTC COD
92492246 9249224 OT
92492246 9249224 HO
92492246 9249224 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
92492246 9249224 Acrochordon
92492246 9249224 Ankle fracture
92492246 9249224 Anxiety
92492246 9249224 Brain injury
92492246 9249224 Cognitive disorder
92492246 9249224 Depression
92492246 9249224 Dermatitis
92492246 9249224 Ejaculation disorder
92492246 9249224 Erectile dysfunction
92492246 9249224 Genital disorder male
92492246 9249224 Genital hypoaesthesia
92492246 9249224 Gynaecomastia
92492246 9249224 Head injury
92492246 9249224 Hormone level abnormal
92492246 9249224 Loss of libido
92492246 9249224 Penis injury
92492246 9249224 Rectal haemorrhage
92492246 9249224 Semen volume decreased
92492246 9249224 Sexual dysfunction
92492246 9249224 Shoulder operation
92492246 9249224 Tibia fracture

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
92492246 9249224 1 200301 20080315 0