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
115207868 11520786 8 F 20140605 20160902 20150918 20160909 EXP PHHO2015NL014251 NOVARTIS 66.08 YR M Y 82.00000 KG 20160909 MD NL NL

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
115207868 11520786 1 PS TASIGNA NILOTINIB 1 Oral 300 MG, BID 365400 MG Y 22068 300 MG CAPSULE BID
115207868 11520786 2 SS DASATINIB DASATINIB 1 Unknown 100 MG, QD 4800 MG Y 0 100 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115207868 11520786 1 Chronic myeloid leukaemia
115207868 11520786 2 Chronic myeloid leukaemia

Outcome of event

Event ID CASEID OUTC COD
115207868 11520786 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
115207868 11520786 Atrial flutter
115207868 11520786 Coronary artery stenosis
115207868 11520786 Fatigue
115207868 11520786 Groin pain
115207868 11520786 Muscle spasms
115207868 11520786 Nausea

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
115207868 11520786 1 20130815 20150415 0
115207868 11520786 2 20150416 20150602 0