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
122677882 12267788 2 F 20150412 20160802 20160414 20160804 EXP US-JNJFOC-20160404805 JANSSEN 77.00 YR E M Y 102.00000 KG 20160804 CN 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
122677882 12267788 1 PS ABIRATERONE ACETATE ABIRATERONE ACETATE 1 Oral N 202379 1000 MG TABLET QD
122677882 12267788 2 SS ENZALUTAMIDE ENZALUTAMIDE 1 Oral 0 80 MG UNSPECIFIED QD
122677882 12267788 3 SS PREDNISONE. PREDNISONE 1 Oral 0 5 MG UNSPECIFIED BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122677882 12267788 1 Hormone-refractory prostate cancer
122677882 12267788 2 Hormone-refractory prostate cancer
122677882 12267788 3 Hormone-refractory prostate cancer

Outcome of event

Event ID CASEID OUTC COD
122677882 12267788 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122677882 12267788 Dyspnoea
122677882 12267788 Gastritis
122677882 12267788 Hypotension
122677882 12267788 Malaise
122677882 12267788 Nephrolithiasis

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
122677882 12267788 1 20140728 0
122677882 12267788 2 20140728 0
122677882 12267788 3 20140728 0