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
91640484 9164048 4 F 2002 20160912 20130314 20160919 EXP US-009507513-1303USA006762 MERCK 0.00 M Y 95.24000 KG 20160919 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
91640484 9164048 1 PS PROPECIA FINASTERIDE 1 Oral 1 MG, QD 3555 MG U 20788 1 MG FILM-COATED TABLET QD
91640484 9164048 2 C ZETIA EZETIMIBE 1 Oral UNK U 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
91640484 9164048 1 Androgenetic alopecia
91640484 9164048 2 Blood cholesterol increased

Outcome of event

Event ID CASEID OUTC COD
91640484 9164048 DS
91640484 9164048 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
91640484 9164048 Benign prostatic hyperplasia
91640484 9164048 Cancer surgery
91640484 9164048 Cataract operation
91640484 9164048 Cerebrovascular accident
91640484 9164048 Cognitive disorder
91640484 9164048 Colectomy
91640484 9164048 Depression
91640484 9164048 Drug hypersensitivity
91640484 9164048 Erectile dysfunction
91640484 9164048 Gynaecomastia
91640484 9164048 Hernia repair
91640484 9164048 Hip arthroplasty
91640484 9164048 Knee operation
91640484 9164048 Libido decreased
91640484 9164048 Organic erectile dysfunction
91640484 9164048 Penile prosthesis insertion
91640484 9164048 Semen volume decreased
91640484 9164048 Sexual dysfunction
91640484 9164048 Squamous cell carcinoma

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
91640484 9164048 1 20020226 20111120 0