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
122176134 12217613 4 F 20160208 20160803 20160329 20160808 EXP PHHY2016IL024985 NOVARTIS 80.69 YR F Y 56.00000 KG 20160808 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
122176134 12217613 1 PS TASIGNA NILOTINIB 1 Oral 200 MG, QD S0127 22068 200 MG CAPSULE QD
122176134 12217613 2 SS TASIGNA NILOTINIB 1 Oral 300 MG, BID 22068 300 MG CAPSULE BID
122176134 12217613 3 C ENSURE AMINO ACIDSDEXTROSEELECTROLYTES NOSSOYBEAN OILVITAMINS 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122176134 12217613 1 Chronic myeloid leukaemia
122176134 12217613 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
122176134 12217613 Asthenia
122176134 12217613 Back pain
122176134 12217613 Concomitant disease aggravated
122176134 12217613 Constipation
122176134 12217613 Decreased appetite
122176134 12217613 Depression
122176134 12217613 Diarrhoea
122176134 12217613 Discomfort
122176134 12217613 Fatigue
122176134 12217613 Gait disturbance
122176134 12217613 Musculoskeletal pain
122176134 12217613 Skin lesion
122176134 12217613 Underdose
122176134 12217613 Weight decreased

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
122176134 12217613 1 20160208 0