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
119217613 11921761 3 F 20151219 20160711 20160115 20160726 EXP PHHY2016TW001686 NOVARTIS 39.76 YR M Y 69.00000 KG 20160726 MD TW TW

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
119217613 11921761 1 PS TASIGNA NILOTINIB 1 Oral 300 MG, BID U 22068 300 MG CAPSULE BID
119217613 11921761 2 SS TASIGNA NILOTINIB 1 Oral 300 MG, BID U 22068 300 MG CAPSULE BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119217613 11921761 1 Chronic myeloid leukaemia

Outcome of event

Event ID CASEID OUTC COD
119217613 11921761 HO
119217613 11921761 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119217613 11921761 Cellulitis
119217613 11921761 Constipation
119217613 11921761 Erythema
119217613 11921761 Eye pain
119217613 11921761 Eye swelling
119217613 11921761 Leukocytosis
119217613 11921761 Pain in extremity
119217613 11921761 Peripheral swelling
119217613 11921761 Septal panniculitis

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
119217613 11921761 1 20151217 0
119217613 11921761 2 20151218 0