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
88345905 8834590 5 F 2007 20160711 20121010 20160714 EXP US-009507513-1210USA003229 MERCK 0.00 M Y 79.37000 KG 20160714 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
88345905 8834590 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
88345905 8834590 1 Androgenetic alopecia

Outcome of event

Event ID CASEID OUTC COD
88345905 8834590 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
88345905 8834590 Androgen deficiency
88345905 8834590 Blood cholesterol increased
88345905 8834590 Cognitive disorder
88345905 8834590 Depression
88345905 8834590 Erectile dysfunction
88345905 8834590 Fatigue
88345905 8834590 Generalised anxiety disorder
88345905 8834590 Insomnia
88345905 8834590 Libido decreased
88345905 8834590 Malaise
88345905 8834590 Sexual dysfunction
88345905 8834590 Skin lesion
88345905 8834590 Stress
88345905 8834590 Suicidal ideation
88345905 8834590 Upper respiratory tract infection

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
88345905 8834590 1 20060131 201110 0