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 |