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
124399442 12439944 2 F 20150709 20160714 20160606 20160721 EXP PHHY2016DE075985 NOVARTIS 0.00 A M Y 0.00000 20160721 MD DE DE

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
124399442 12439944 1 PS TASIGNA NILOTINIB 1 Unknown 600 MG, QD 2400 MG U 22068 600 MG CAPSULE QD
124399442 12439944 2 SS TASIGNA NILOTINIB 1 Unknown 300 MG, BID 2400 MG U 22068 300 MG CAPSULE BID
124399442 12439944 3 C METOCLOPRAMIDE. METOCLOPRAMIDE 1 Unknown AS REQUESTED U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124399442 12439944 1 Chronic myeloid leukaemia
124399442 12439944 3 Nausea

Outcome of event

Event ID CASEID OUTC COD
124399442 12439944 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124399442 12439944 Angina pectoris
124399442 12439944 Nausea
124399442 12439944 Vomiting

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
124399442 12439944 1 20150706 20150714 0
124399442 12439944 2 20150717 0
124399442 12439944 3 20151116 0