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
90565766 9056576 6 F 200808 20160727 20130204 20160803 EXP US-009507513-1302USA000373 MERCK 0.00 M Y 0.00000 20160803 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
90565766 9056576 1 PS PROPECIA FINASTERIDE 1 Oral 1 MG, UNK U 20788 1 MG FILM-COATED TABLET
90565766 9056576 2 SS FINASTERIDE. FINASTERIDE 1 Oral 5 MG, UNK U 0 5 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
90565766 9056576 1 Alopecia
90565766 9056576 2 Alopecia

Outcome of event

Event ID CASEID OUTC COD
90565766 9056576 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
90565766 9056576 Anger
90565766 9056576 Anxiety
90565766 9056576 Cognitive disorder
90565766 9056576 Depression
90565766 9056576 Drug administration error
90565766 9056576 Erectile dysfunction
90565766 9056576 Knee operation
90565766 9056576 Limb operation
90565766 9056576 Mood altered
90565766 9056576 Sexual dysfunction

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
90565766 9056576 1 20080722 20120720 0
90565766 9056576 2 20080722 20151231 0