The Safety Rates Drug Report

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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
118300844 11830084 4 F 20151028 20160718 20151213 20160720 EXP PHHY2015CA161338 NOVARTIS 22.03 YR F Y 0.00000 20160720 CN COUNTRY NOT SPECIFIED CA

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
118300844 11830084 1 PS TASIGNA NILOTINIB 1 Oral 400 MG, BID Y 22068 400 MG CAPSULE BID
118300844 11830084 2 C PREGABALIN. PREGABALIN 1 Unknown U 0
118300844 11830084 3 C ABILIFY ARIPIPRAZOLE 1 Unknown U 0
118300844 11830084 4 C MIRTAZAPINE. MIRTAZAPINE 1 Unknown U 0
118300844 11830084 5 C BISOPROLOL BISOPROLOL 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118300844 11830084 1 Chronic myeloid leukaemia
118300844 11830084 2 Product used for unknown indication
118300844 11830084 3 Product used for unknown indication
118300844 11830084 4 Product used for unknown indication
118300844 11830084 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
118300844 11830084 Decreased appetite
118300844 11830084 Fatigue
118300844 11830084 Nausea
118300844 11830084 Vomiting
118300844 11830084 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
118300844 11830084 1 20151028 0