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
92180505 9218050 5 F 2009 20160727 20130408 20160801 EXP US-009507513-1304USA002497 MERCK 0.00 M Y 95.24000 KG 20160801 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
92180505 9218050 1 PS PROPECIA FINASTERIDE 1 Oral 1 MG, QD 3308 MG 20788 1 MG FILM-COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
92180505 9218050 1 Alopecia

Outcome of event

Event ID CASEID OUTC COD
92180505 9218050 OT
92180505 9218050 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
92180505 9218050 Anxiety
92180505 9218050 Cardiac disorder
92180505 9218050 Cognitive disorder
92180505 9218050 Fatigue
92180505 9218050 Hypercholesterolaemia
92180505 9218050 Hyperlipidaemia
92180505 9218050 Hypertension
92180505 9218050 Hypogonadism male
92180505 9218050 Infertility
92180505 9218050 Loss of libido
92180505 9218050 Myocardial infarction
92180505 9218050 Organic erectile dysfunction
92180505 9218050 Partner stress
92180505 9218050 Penis injury
92180505 9218050 Sexual dysfunction

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
92180505 9218050 1 20030509 20120528 0