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
92457918 9245791 8 F 2010 20160804 20130422 20160809 EXP US-009507513-1112USA02606 MERCK 0.00 M Y 0.00000 20160809 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
92457918 9245791 1 PS PROPECIA FINASTERIDE 1 Oral 1 MG, QD 380 MG 20788 1 MG FILM-COATED TABLET QD
92457918 9245791 2 SS PROPECIA FINASTERIDE 1 380 MG 20788 FILM-COATED TABLET
92457918 9245791 3 C RITALIN METHYLPHENIDATE HYDROCHLORIDE 1 Unknown UNK, UNKNOWN U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
92457918 9245791 1 Alopecia
92457918 9245791 2 Androgenetic alopecia
92457918 9245791 3 Autism

Outcome of event

Event ID CASEID OUTC COD
92457918 9245791 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
92457918 9245791 Amnesia
92457918 9245791 Anxiety
92457918 9245791 Attention deficit/hyperactivity disorder
92457918 9245791 Bladder outlet obstruction
92457918 9245791 Cognitive disorder
92457918 9245791 Depression
92457918 9245791 Diarrhoea
92457918 9245791 Drug ineffective
92457918 9245791 Erectile dysfunction
92457918 9245791 Headache
92457918 9245791 Hypertonic bladder
92457918 9245791 Lower urinary tract symptoms
92457918 9245791 Paraesthesia
92457918 9245791 Pelvic floor muscle weakness
92457918 9245791 Penile size reduced
92457918 9245791 Prostatitis
92457918 9245791 Prostatomegaly
92457918 9245791 Sexual dysfunction
92457918 9245791 Terminal dribbling
92457918 9245791 Urinary tract obstruction
92457918 9245791 Urine flow decreased

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
92457918 9245791 1 20100713 20110727 0
92457918 9245791 3 2008 0