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
109781066 10978106 6 F 20150110 20160721 20150402 20160724 EXP PHHY2015KR003705 NOVARTIS 72.86 YR M Y 0.00000 20160724 CN COUNTRY NOT SPECIFIED KR

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
109781066 10978106 1 PS TASIGNA NILOTINIB 1 Oral 400 MG, BID 22068 400 MG CAPSULE BID
109781066 10978106 2 SS GLIVEC IMATINIB MESYLATE 1 Oral 400 MG, QD 0 400 MG TABLET QD
109781066 10978106 3 SS SPRYCEL DASATINIB 1 Oral QD Y 0 TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109781066 10978106 1 Chronic myeloid leukaemia
109781066 10978106 2 Chronic myeloid leukaemia
109781066 10978106 3 Chronic myeloid leukaemia

Outcome of event

Event ID CASEID OUTC COD
109781066 10978106 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
109781066 10978106 Arthralgia
109781066 10978106 Asthenia
109781066 10978106 Dyspnoea
109781066 10978106 Facial paralysis
109781066 10978106 Faeces discoloured
109781066 10978106 Gallbladder disorder
109781066 10978106 Herpes zoster
109781066 10978106 Hypoaesthesia
109781066 10978106 Immunodeficiency
109781066 10978106 Nausea
109781066 10978106 Panic disorder
109781066 10978106 Stress

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
109781066 10978106 1 2012 0
109781066 10978106 2 2006 0
109781066 10978106 3 2012 0