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
126182982 12618298 2 F 20151016 20160825 20160803 20160901 EXP PHHY2015CO136842 NOVARTIS 40.94 YR M Y 75.00000 KG 20160901 CN COUNTRY NOT SPECIFIED CO

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
126182982 12618298 1 PS TASIGNA NILOTINIB 1 Oral 600 MG, QD (2 DF IN THE MORNING AND 1 DF IN THE AFTERNOON) U 22068 600 MG CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126182982 12618298 1 Chronic myeloid leukaemia

Outcome of event

Event ID CASEID OUTC COD
126182982 12618298 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126182982 12618298 Abdominal pain
126182982 12618298 Back pain
126182982 12618298 Blast crisis in myelogenous leukaemia
126182982 12618298 Chikungunya virus infection
126182982 12618298 Cough
126182982 12618298 Headache
126182982 12618298 Nausea
126182982 12618298 Nephrolithiasis
126182982 12618298 Pain
126182982 12618298 Pyrexia
126182982 12618298 Radiation associated pain
126182982 12618298 Rash

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
126182982 12618298 1 20150703 0