The Safety Rates Drug Report

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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
115023302 11502330 2 F 20151215 20150914 20160915 PER US-ASTELLAS-2015US019879 ASTELLAS 0.00 M Y 0.00000 20160915 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
115023302 11502330 1 PS XTANDI ENZALUTAMIDE 1 Oral Y 203415 160 MG CAPSULE QD
115023302 11502330 2 SS XTANDI ENZALUTAMIDE 1 203415 CAPSULE
115023302 11502330 3 SS FLOMAX TAMSULOSIN HYDROCHLORIDE 1 Unknown UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115023302 11502330 1 Hormone-refractory prostate cancer
115023302 11502330 2 Prostate cancer
115023302 11502330 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
115023302 11502330 Decreased appetite
115023302 11502330 Dizziness
115023302 11502330 Fatigue

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
115023302 11502330 1 20150512 0