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
118843813 11884381 3 F 20160828 20160103 20160901 EXP PHHY2013IL096439 NOVARTIS 0.00 F Y 86.00000 KG 20160902 CN COUNTRY NOT SPECIFIED IL

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
118843813 11884381 1 PS TASIGNA NILOTINIB 1 Oral 400 MG, BID S0127 22068 400 MG CAPSULE BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118843813 11884381 1 Chronic myeloid leukaemia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
118843813 11884381 Back pain
118843813 11884381 Ear infection
118843813 11884381 Increased appetite
118843813 11884381 Pain in extremity
118843813 11884381 Peripheral swelling
118843813 11884381 Varicose vein

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
118843813 11884381 1 2010 0