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
110264444 11026444 4 F 2000 20160628 20150414 20160701 EXP US-009507513-1504USA005260 MERCK 0.00 M Y 0.00000 20160701 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
110264444 11026444 1 PS PROPECIA FINASTERIDE 1 Oral UNK UNK, QD U 20788 FILM-COATED TABLET QD
110264444 11026444 2 SS PROPECIA FINASTERIDE 1 Oral 1 MG, UNK U 20788 1 MG FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
110264444 11026444 1 Androgenetic alopecia

Outcome of event

Event ID CASEID OUTC COD
110264444 11026444 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
110264444 11026444 Acute stress disorder
110264444 11026444 Basal cell carcinoma
110264444 11026444 Hyperlipidaemia
110264444 11026444 Hypertension
110264444 11026444 Hypertriglyceridaemia
110264444 11026444 Hypokalaemia
110264444 11026444 Intervertebral disc protrusion
110264444 11026444 Lumbar spinal stenosis
110264444 11026444 Melanocytic naevus
110264444 11026444 Myocardial ischaemia
110264444 11026444 Nephrolithiasis
110264444 11026444 Organic erectile dysfunction
110264444 11026444 Polycythaemia
110264444 11026444 Prostatic specific antigen increased
110264444 11026444 Sciatica
110264444 11026444 Sexual dysfunction
110264444 11026444 Sperm concentration decreased

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
110264444 11026444 1 1999 2000 0
110264444 11026444 2 2000 2005 0