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
101749818 10174981 8 F 20131109 20160805 20140515 20160810 EXP PHHY2013IT151016 NOVARTIS 50.18 YR F Y 0.00000 20160810 OT IT IT

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
101749818 10174981 1 PS TASIGNA NILOTINIB 1 Oral 600 MG, BID 22068 600 MG CAPSULE BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
101749818 10174981 1 Chronic myeloid leukaemia

Outcome of event

Event ID CASEID OUTC COD
101749818 10174981 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
101749818 10174981 Blister
101749818 10174981 Conjunctivitis
101749818 10174981 Escherichia urinary tract infection
101749818 10174981 Foot fracture
101749818 10174981 Hypertension
101749818 10174981 Influenza
101749818 10174981 Lymphadenitis
101749818 10174981 Oropharyngeal pain
101749818 10174981 Pruritus
101749818 10174981 Rhinitis
101749818 10174981 Upper respiratory tract infection
101749818 10174981 Urinary tract infection

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
101749818 10174981 1 20101218 0