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
100738373 10073837 3 F 2003 20160914 20140413 20160921 EXP US-009507513-1404USA004029 MERCK 0.00 M Y 0.00000 20160921 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
100738373 10073837 1 PS PROPECIA FINASTERIDE 1 Oral 1 MG, UNK 20788 1 MG FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100738373 10073837 1 Androgenetic alopecia

Outcome of event

Event ID CASEID OUTC COD
100738373 10073837 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
100738373 10073837 Anxiety
100738373 10073837 Blood testosterone decreased
100738373 10073837 Cognitive disorder
100738373 10073837 Depression
100738373 10073837 Emotional distress
100738373 10073837 Epilepsy
100738373 10073837 Erectile dysfunction
100738373 10073837 Fatigue
100738373 10073837 Head injury
100738373 10073837 Hyperlipidaemia
100738373 10073837 Hypertension
100738373 10073837 Libido decreased
100738373 10073837 Microalbuminuria
100738373 10073837 Nephrolithiasis
100738373 10073837 Neuropathy peripheral
100738373 10073837 Panic attack
100738373 10073837 Pyrexia
100738373 10073837 Seizure
100738373 10073837 Sexual dysfunction
100738373 10073837 Squamous cell carcinoma of the tongue
100738373 10073837 Treatment noncompliance
100738373 10073837 Type 2 diabetes mellitus

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
100738373 10073837 1 1997 20070726 0