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
107427605 10742760 5 F 20061002 20160711 20150127 20160714 EXP US-009507513-1204USA02818 MERCK 0.00 M Y 0.00000 20160714 PH 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
107427605 10742760 1 PS PROPECIA FINASTERIDE 1 Oral UNK 20788 FILM-COATED TABLET
107427605 10742760 2 SS 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
107427605 10742760 1 Androgenetic alopecia
107427605 10742760 2 Alopecia

Outcome of event

Event ID CASEID OUTC COD
107427605 10742760 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
107427605 10742760 Anxiety
107427605 10742760 Cognitive disorder
107427605 10742760 Depression
107427605 10742760 Drug ineffective
107427605 10742760 Erectile dysfunction
107427605 10742760 Fatigue
107427605 10742760 Furuncle
107427605 10742760 Hypogonadism
107427605 10742760 Insomnia
107427605 10742760 Irritability
107427605 10742760 Libido decreased
107427605 10742760 Metabolic syndrome
107427605 10742760 Sexual dysfunction
107427605 10742760 Staphylococcal infection
107427605 10742760 Testicular failure
107427605 10742760 Urine flow decreased
107427605 10742760 Weight increased

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
107427605 10742760 2 20061102 20080314 0