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
110274315 11027431 5 F 2002 20160829 20150414 20160901 EXP US-009507513-1504USA010725 MERCK 0.00 M Y 71.66000 KG 20160901 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
110274315 11027431 1 PS PROPECIA FINASTERIDE 1 Oral 1 MG, QD 20788 1 MG FILM-COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
110274315 11027431 1 Androgenetic alopecia

Outcome of event

Event ID CASEID OUTC COD
110274315 11027431 OT
110274315 11027431 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
110274315 11027431 Arthropathy
110274315 11027431 Brain injury
110274315 11027431 Depression
110274315 11027431 Ejaculation disorder
110274315 11027431 Endocrine disorder
110274315 11027431 Erectile dysfunction
110274315 11027431 Essential hypertension
110274315 11027431 Hormone level abnormal
110274315 11027431 Hypogonadism
110274315 11027431 Loss of libido
110274315 11027431 Lung carcinoma cell type unspecified stage III
110274315 11027431 Osteoarthritis
110274315 11027431 Painful ejaculation
110274315 11027431 Penile size reduced
110274315 11027431 Penis injury
110274315 11027431 Plasma cell myeloma
110274315 11027431 Rheumatoid arthritis
110274315 11027431 Sexual dysfunction
110274315 11027431 Sleep apnoea syndrome
110274315 11027431 Systemic lupus erythematosus
110274315 11027431 Testicular disorder

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
110274315 11027431 1 2002 2005 0