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
122906343 12290634 3 F 20151105 20160617 20160421 20160720 EXP PHHY2016KR053486 NOVARTIS 52.25 YR F Y 0.00000 20160720 MD KR 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
122906343 12290634 1 PS TASIGNA NILOTINIB 1 Oral 600 MG, QD 35400 MG U 22068 600 MG CAPSULE QD
122906343 12290634 2 SS TASIGNA NILOTINIB 1 Oral 400 MG, QD 35400 MG U 22068 400 MG CAPSULE QD
122906343 12290634 3 C HYDROCORTISONE. HYDROCORTISONE 1 Intravenous (not otherwise specified) 200 MG, UNK 0 200 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122906343 12290634 1 Chronic myeloid leukaemia
122906343 12290634 3 Prophylaxis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
122906343 12290634 Headache

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
122906343 12290634 1 20150908 20151105 0
122906343 12290634 2 20151215 0
122906343 12290634 3 20151210 20151210 0