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
92499196 9249919 6 F 19990227 20160707 20130423 20160712 EXP US-009507513-1304USA011048 MERCK 0.00 M Y 84.35000 KG 20160712 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
92499196 9249919 1 PS PROPECIA FINASTERIDE 1 Oral 1 MG, QD 20788 1 MG FILM-COATED TABLET QD
92499196 9249919 2 SS PROPECIA FINASTERIDE 1 Oral 1 MG, ONE DAILY 20788 1 MG FILM-COATED TABLET QD
92499196 9249919 3 SS EFFEXOR VENLAFAXINE HYDROCHLORIDE 1 Oral 150 MG, UNK 0 150 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
92499196 9249919 1 Androgenetic alopecia

Outcome of event

Event ID CASEID OUTC COD
92499196 9249919 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
92499196 9249919 Alcohol abuse
92499196 9249919 Anxiety
92499196 9249919 Attention deficit/hyperactivity disorder
92499196 9249919 Cognitive disorder
92499196 9249919 Depression
92499196 9249919 Erectile dysfunction
92499196 9249919 Hypertension
92499196 9249919 Libido decreased
92499196 9249919 Ligament operation
92499196 9249919 Muscle strain
92499196 9249919 Obesity
92499196 9249919 Peyronie's disease
92499196 9249919 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
92499196 9249919 1 19981001 0
92499196 9249919 2 20000524 201208 0
92499196 9249919 3 200911 201108 0