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
120049044 12004904 4 F 2014 20160919 20160204 20160926 EXP PHHY2015KR006708 NOVARTIS 53.94 YR F Y 0.00000 20160926 CN COUNTRY NOT SPECIFIED KR

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
120049044 12004904 1 PS GLIVEC IMATINIB MESYLATE 1 Oral 400 MG, QD D 21588 400 MG TABLET QD
120049044 12004904 2 SS TASIGNA NILOTINIB 1 Oral 400 MG, BID Y 0 400 MG CAPSULE BID
120049044 12004904 3 SS TASIGNA NILOTINIB 1 Oral 300 MG, BID Y 0 300 MG CAPSULE BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120049044 12004904 1 Chronic myeloid leukaemia
120049044 12004904 2 Chronic myeloid leukaemia

Outcome of event

Event ID CASEID OUTC COD
120049044 12004904 HO
120049044 12004904 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
120049044 12004904 Alopecia
120049044 12004904 Arthralgia
120049044 12004904 Arthritis
120049044 12004904 Chills
120049044 12004904 Depressed mood
120049044 12004904 Diabetes mellitus
120049044 12004904 Haematuria
120049044 12004904 Hyperlipidaemia
120049044 12004904 Polyuria

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
120049044 12004904 1 20080328 20120622 0
120049044 12004904 2 20120623 0