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
125266022 12526602 2 F 20111007 20160708 20160705 20160714 EXP PHJP2016JP018871 NOVARTIS 56.00 YR M Y 0.00000 20160714 MD JP JP

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
125266022 12526602 1 PS TASIGNA NILOTINIB 1 Oral 600 MG, QD Y 22068 600 MG CAPSULE QD
125266022 12526602 2 C AMLODIPINE AMLODIPINE BESYLATE 1 Oral 5 MG, UNK U 0 5 MG
125266022 12526602 3 C CARVEDILOL. CARVEDILOL 1 Oral 10 MG, UNK U 0 10 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125266022 12526602 1 Chronic myeloid leukaemia
125266022 12526602 2 Hypertension
125266022 12526602 3 Hypertension

Outcome of event

Event ID CASEID OUTC COD
125266022 12526602 OT
125266022 12526602 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125266022 12526602 Angina pectoris
125266022 12526602 Arteriosclerosis
125266022 12526602 Arteriosclerosis coronary artery
125266022 12526602 Chest pain
125266022 12526602 Coronary artery stenosis
125266022 12526602 Myocardial ischaemia

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
125266022 12526602 1 201102 201408 0