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
127235851 12723585 1 I 20160406 20160802 20160908 20160908 EXP US-JNJFOC-20160801642 JANSSEN 91.00 YR E M Y 71.00000 KG 20160908 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
127235851 12723585 1 PS ZYTIGA ABIRATERONE ACETATE 1 Oral N 202379 1000 MG TABLET
127235851 12723585 2 SS ENZALUTAMIDE ENZALUTAMIDE 1 Oral Y 0 160 MG UNSPECIFIED QD
127235851 12723585 3 SS PREDNISONE. PREDNISONE 1 Oral Y 0 5 MG UNSPECIFIED BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127235851 12723585 1 Prostate cancer metastatic
127235851 12723585 2 Prostate cancer metastatic
127235851 12723585 3 Prostate cancer metastatic

Outcome of event

Event ID CASEID OUTC COD
127235851 12723585 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127235851 12723585 Atrial fibrillation
127235851 12723585 Cardiac failure congestive
127235851 12723585 Dizziness
127235851 12723585 Dyspnoea
127235851 12723585 Muscular weakness
127235851 12723585 Pneumonia
127235851 12723585 Urinary tract infection

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
127235851 12723585 1 20160316 20160405 0
127235851 12723585 2 20160316 20160406 0
127235851 12723585 3 20160316 20160406 0