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
109715693 10971569 3 F 2001 20160630 20150331 20160701 EXP US-009507513-1503USA014205 MERCK 0.00 M Y 92.63000 KG 20160701 LW 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
109715693 10971569 1 PS PROPECIA FINASTERIDE 1 Oral 1 MG, QD 20788 1 MG FILM-COATED TABLET QD
109715693 10971569 2 SS PROPECIA FINASTERIDE 1 20788 FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109715693 10971569 1 Androgenetic alopecia
109715693 10971569 2 Alopecia

Outcome of event

Event ID CASEID OUTC COD
109715693 10971569 OT
109715693 10971569 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
109715693 10971569 Anxiety
109715693 10971569 Asthenia
109715693 10971569 Cardiac murmur
109715693 10971569 Cognitive disorder
109715693 10971569 Depression
109715693 10971569 Erectile dysfunction
109715693 10971569 Feeling abnormal
109715693 10971569 Hepatitis C
109715693 10971569 Hypercholesterolaemia
109715693 10971569 Libido decreased
109715693 10971569 Limb operation
109715693 10971569 Muscle spasms
109715693 10971569 Osteoarthritis
109715693 10971569 Pruritus
109715693 10971569 Rash
109715693 10971569 Sciatica
109715693 10971569 Semen analysis abnormal
109715693 10971569 Semen volume decreased
109715693 10971569 Sexual dysfunction
109715693 10971569 Testicular pain

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
109715693 10971569 1 1998 200911 0