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
101005876 10100587 6 F 2008 20160714 20140423 20160721 EXP US-009507513-1103USA03951 MERCK 0.00 M Y 66.21000 KG 20160721 CN 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
101005876 10100587 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
101005876 10100587 1 Androgenetic alopecia

Outcome of event

Event ID CASEID OUTC COD
101005876 10100587 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
101005876 10100587 Anxiety
101005876 10100587 Dehydration
101005876 10100587 Depression
101005876 10100587 Dysuria
101005876 10100587 Emotional distress
101005876 10100587 Epididymal cyst
101005876 10100587 Erectile dysfunction
101005876 10100587 Food poisoning
101005876 10100587 Hydrocele
101005876 10100587 Libido decreased
101005876 10100587 Libido increased
101005876 10100587 Orgasmic sensation decreased
101005876 10100587 Scrotal pain
101005876 10100587 Scrotal swelling
101005876 10100587 Semen volume decreased
101005876 10100587 Sexual dysfunction
101005876 10100587 Testicular disorder
101005876 10100587 Testicular pain
101005876 10100587 Varicocele

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
101005876 10100587 1 20080213 200806 0