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
124856912 12485691 2 F 20160605 20160913 20160621 20160919 EXP PHHY2016VE085230 NOVARTIS 44.62 YR F Y 0.00000 20160919 CN COUNTRY NOT SPECIFIED VE

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
124856912 12485691 1 PS TASIGNA NILOTINIB 1 Oral 800 MG, QD 22068 800 MG CAPSULE QD
124856912 12485691 2 I TASIGNA NILOTINIB 1 Oral 800 MG, QD 22068 800 MG CAPSULE QD
124856912 12485691 3 I ATAMEL ACETAMINOPHEN 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124856912 12485691 1 Chronic myeloid leukaemia
124856912 12485691 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124856912 12485691 Drug interaction
124856912 12485691 Hypersensitivity
124856912 12485691 Pain in extremity

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
124856912 12485691 1 20160523 201606 0
124856912 12485691 2 20160614 0