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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120890104 | 12089010 | 4 | F | 20160215 | 20160907 | 20160218 | 20160913 | EXP | PHHY2016CO021681 | NOVARTIS | 86.21 | YR | F | Y | 50.00000 | KG | 20160913 | CN | COUNTRY NOT SPECIFIED | CO |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120890104 | 12089010 | 1 | PS | TASIGNA | NILOTINIB | 1 | Oral | 200 MG, BID | 22068 | 200 | MG | CAPSULE | BID | ||||||
| 120890104 | 12089010 | 2 | C | LOSARTAN. | LOSARTAN | 1 | Oral | 50 MG, BID | U | 0 | 50 | MG | TABLET | BID | |||||
| 120890104 | 12089010 | 3 | C | METOPROLOL. | METOPROLOL | 1 | Oral | 0.5 DF, Q8H | U | 0 | .5 | DF | TABLET | Q8H | |||||
| 120890104 | 12089010 | 4 | C | NIFEDIPINE. | NIFEDIPINE | 1 | Oral | 30 MG, QD | U | 0 | 30 | MG | TABLET | QD | |||||
| 120890104 | 12089010 | 5 | C | CLOPIDOGREL | CLOPIDOGREL BISULFATE | 1 | Unknown | U | 0 | ||||||||||
| 120890104 | 12089010 | 6 | C | FUROSEMIDE. | FUROSEMIDE | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 120890104 | 12089010 | 1 | Chronic myeloid leukaemia |
| 120890104 | 12089010 | 2 | Blood pressure abnormal |
| 120890104 | 12089010 | 3 | Product used for unknown indication |
| 120890104 | 12089010 | 4 | Product used for unknown indication |
| 120890104 | 12089010 | 5 | Product used for unknown indication |
| 120890104 | 12089010 | 6 | Fluid retention |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 120890104 | 12089010 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 120890104 | 12089010 | Depressed mood | |
| 120890104 | 12089010 | Erythema | |
| 120890104 | 12089010 | Fatigue | |
| 120890104 | 12089010 | General physical health deterioration | |
| 120890104 | 12089010 | Malaise | |
| 120890104 | 12089010 | Pyrexia | |
| 120890104 | 12089010 | Therapy non-responder | |
| 120890104 | 12089010 | Viral infection |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |