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
111999074 11199907 4 F 20150602 20160809 20150618 20160816 EXP US-ARIAD-2015US004779 ARIAD 68.79 YR F Y 59.41000 KG 20160816 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
111999074 11199907 1 PS ICLUSIG PONATINIB 1 Oral 30 MG, QD Y U 31L14E01 203469 30 MG TABLET
111999074 11199907 2 SS ICLUSIG PONATINIB 1 Oral 45 MG, QD Y U 31L14E01 203469 45 MG TABLET
111999074 11199907 3 SS TASIGNA NILOTINIB 1 0
111999074 11199907 4 SS Hyper CVAD CYCLOPHOSPHAMIDECYTARABINEDEXAMETHASONEDOXORUBICINMETHOTREXATEVINCRISTINE 1 0
111999074 11199907 5 SS Blinatumomab BLINATUMOMAB 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
111999074 11199907 1 Acute lymphocytic leukaemia

Outcome of event

Event ID CASEID OUTC COD
111999074 11199907 OT
111999074 11199907 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
111999074 11199907 Blood lactate dehydrogenase increased
111999074 11199907 Chills
111999074 11199907 Device related thrombosis
111999074 11199907 Hypoaesthesia
111999074 11199907 Muscular weakness
111999074 11199907 Nausea
111999074 11199907 Neoplasm progression
111999074 11199907 Packed red blood cell transfusion
111999074 11199907 Pain in extremity
111999074 11199907 Pyrexia
111999074 11199907 Thrombocytopenia
111999074 11199907 Weight decreased

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
111999074 11199907 1 20150403 0