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
105653407 10565340 7 F 20160808 20141105 20160810 EXP PHHY2013IL113153 NOVARTIS 0.00 M Y 110.00000 KG 20160810 CN IL 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
105653407 10565340 1 PS TASIGNA NILOTINIB 1 Oral 2 DF, BID (400MG AT THE MORNING+200MG AT THE EVENING) S0077 22068 2 DF CAPSULE BID
105653407 10565340 2 SS TASIGNA NILOTINIB 1 Oral 600 MG,(400MG AT THE MORNING AND 200 MG AT EVENING) 22068 600 MG CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
105653407 10565340 1 Chronic myeloid leukaemia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
105653407 10565340 Back pain
105653407 10565340 Blood glucose increased
105653407 10565340 Dysgeusia
105653407 10565340 Dyspepsia
105653407 10565340 Fatigue
105653407 10565340 Insomnia
105653407 10565340 Leukocytosis
105653407 10565340 Nausea
105653407 10565340 Urinary tract infection
105653407 10565340 Weight decreased
105653407 10565340 Wound

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
105653407 10565340 1 20130901 0