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
970800513 9708005 13 F 20010213 20160629 20131125 20160707 EXP US-MERCK-1311USA008145 MERCK 0.00 M Y 99.77000 KG 20160707 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
970800513 9708005 1 PS PROPECIA FINASTERIDE 1 Oral 1 MG, QD 20788 1 MG FILM-COATED TABLET QD
970800513 9708005 2 SS PROPECIA FINASTERIDE 1 Oral 1 MG, QD 20788 1 MG FILM-COATED TABLET QD
970800513 9708005 3 SS PROSCAR FINASTERIDE 1 Oral 5 MG, SPLIT INTO 1/5 DAILY 0 5 MG FILM-COATED TABLET QD
970800513 9708005 4 SS FINASTERIDE. FINASTERIDE 1 Oral 5 MG, QD 0 5 MG QD
970800513 9708005 5 SS FINASTERIDE. FINASTERIDE 1 Oral 5 MG, SPLIT INTO 1/5 DAILY 0 5 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
970800513 9708005 1 Androgenetic alopecia
970800513 9708005 3 Alopecia
970800513 9708005 4 Alopecia

Outcome of event

Event ID CASEID OUTC COD
970800513 9708005 DS
970800513 9708005 HO
970800513 9708005 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
970800513 9708005 Acne
970800513 9708005 Alopecia
970800513 9708005 Arthralgia
970800513 9708005 Attention deficit/hyperactivity disorder
970800513 9708005 Blepharitis
970800513 9708005 Blindness
970800513 9708005 Blood testosterone decreased
970800513 9708005 Chronic fatigue syndrome
970800513 9708005 Cognitive disorder
970800513 9708005 Drug administration error
970800513 9708005 Dry eye
970800513 9708005 Dry skin
970800513 9708005 Eczema
970800513 9708005 Ejaculation disorder
970800513 9708005 Epididymal cyst
970800513 9708005 Erectile dysfunction
970800513 9708005 Eye pain
970800513 9708005 Generalised anxiety disorder
970800513 9708005 Hand fracture
970800513 9708005 Headache
970800513 9708005 Heart rate irregular
970800513 9708005 Hydrocele
970800513 9708005 Hypogonadism
970800513 9708005 Lacrimation decreased
970800513 9708005 Libido decreased
970800513 9708005 Major depression
970800513 9708005 Male orgasmic disorder
970800513 9708005 Muscle atrophy
970800513 9708005 Myalgia
970800513 9708005 Obsessive-compulsive disorder
970800513 9708005 Pain in jaw
970800513 9708005 Penile curvature
970800513 9708005 Peyronie's disease
970800513 9708005 Scrotal pain
970800513 9708005 Semen volume decreased
970800513 9708005 Sexual dysfunction
970800513 9708005 Sleep apnoea syndrome
970800513 9708005 Substance dependence
970800513 9708005 Supraventricular tachycardia
970800513 9708005 Tachycardia paroxysmal
970800513 9708005 Testicular pain
970800513 9708005 Tongue movement disturbance
970800513 9708005 Treatment noncompliance
970800513 9708005 Varicocele
970800513 9708005 Varicose vein
970800513 9708005 Vitamin D abnormal
970800513 9708005 Wisdom teeth removal
970800513 9708005 Wrist fracture
970800513 9708005 Wrong technique in product usage process

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
970800513 9708005 1 199812 201111 0
970800513 9708005 2 20101220 20111104 0
970800513 9708005 3 200704 201012 0
970800513 9708005 4 20070319 0
970800513 9708005 5 20100810 20100918 0