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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 121850972 | 12185097 | 2 | F | 20160907 | 20160316 | 20160914 | EXP | PHEH2016US005981 | NOVARTIS | 0.00 | F | Y | 0.00000 | 20160914 | CN | COUNTRY NOT SPECIFIED | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 121850972 | 12185097 | 1 | PS | TASIGNA | NILOTINIB | 1 | Oral | 200 MG, BID | 22068 | 200 | MG | CAPSULE | BID | ||||||
| 121850972 | 12185097 | 2 | SS | TASIGNA | NILOTINIB | 1 | Oral | 200 MG, QID | 22068 | 200 | MG | CAPSULE | QID | ||||||
| 121850972 | 12185097 | 3 | SS | TASIGNA | NILOTINIB | 1 | Oral | 4 DF, QD (TOTAL 800 MG, QD (200 MG, 4 TABLETS A DAY)) | F0047 | 22068 | 4 | DF | CAPSULE | QD | |||||
| 121850972 | 12185097 | 4 | C | VALSARTAN. | VALSARTAN | 1 | Oral | 160 MG, UNK | U | 0 | 160 | MG | |||||||
| 121850972 | 12185097 | 5 | C | ASPIRIN. | ASPIRIN | 1 | Oral | 81 MG, UNK | U | 0 | 81 | MG | |||||||
| 121850972 | 12185097 | 6 | C | HYDROCHLOROTHIAZIDE. | HYDROCHLOROTHIAZIDE | 1 | Unknown | 12.5 MG, UNK | U | 0 | 12.5 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 121850972 | 12185097 | 1 | Product used for unknown indication |
| 121850972 | 12185097 | 4 | Product used for unknown indication |
| 121850972 | 12185097 | 5 | Product used for unknown indication |
| 121850972 | 12185097 | 6 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 121850972 | 12185097 | Dizziness | |
| 121850972 | 12185097 | Drug administration error | |
| 121850972 | 12185097 | Feeling abnormal | |
| 121850972 | 12185097 | Incorrect dose administered | |
| 121850972 | 12185097 | Malaise |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |