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
109834506 10983450 6 F 19980319 20160713 20150403 20160721 EXP US-009507513-98031967 MERCK 0.00 M Y 131.52000 KG 20160721 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
109834506 10983450 1 PS PROPECIA FINASTERIDE 1 Oral 1 MG, UNK U 20788 1 MG FILM-COATED TABLET
109834506 10983450 2 SS PROPECIA FINASTERIDE 1 U 20788 FILM-COATED TABLET
109834506 10983450 3 C TETRACYCLINE TETRACYCLINE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109834506 10983450 1 Alopecia
109834506 10983450 2 Androgenetic alopecia

Outcome of event

Event ID CASEID OUTC COD
109834506 10983450 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
109834506 10983450 Anxiety
109834506 10983450 Arthralgia
109834506 10983450 Benign prostatic hyperplasia
109834506 10983450 Depression
109834506 10983450 Ejaculation disorder
109834506 10983450 Erectile dysfunction
109834506 10983450 Gynaecomastia
109834506 10983450 Hernia repair
109834506 10983450 Hypertension
109834506 10983450 Jaw operation
109834506 10983450 Myalgia
109834506 10983450 Sexual dysfunction
109834506 10983450 Spermatocele

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
109834506 10983450 1 19970820 20101021 0
109834506 10983450 3 1998 0