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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125437141 | 12543714 | 1 | I | 20160608 | 0 | 20160708 | 20160708 | DIR | 57.00 | YR | F | N | 252.00000 | LBS | 20160707 | N | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125437141 | 12543714 | 1 | PS | GLEEVEC | IMATINIB MESYLATE | 1 | Oral | N | D | 0 | 20 | DF | COATED TABLET | QD | |||||
125437141 | 12543714 | 2 | C | PREDNISONE. | PREDNISONE | 1 | 0 | ||||||||||||
125437141 | 12543714 | 3 | C | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | 0 | ||||||||||||
125437141 | 12543714 | 4 | C | PREMARIN | ESTROGENS, CONJUGATED | 1 | 0 | ||||||||||||
125437141 | 12543714 | 5 | C | XIFAXAN | RIFAXIMIN | 1 | 0 | ||||||||||||
125437141 | 12543714 | 6 | C | PROZAC | FLUOXETINE HYDROCHLORIDE | 1 | 0 | ||||||||||||
125437141 | 12543714 | 7 | C | TRAZODONE | TRAZODONE HYDROCHLORIDE | 1 | 0 | ||||||||||||
125437141 | 12543714 | 8 | C | VISTARIL | HYDROXYZINE PAMOATE | 1 | 0 | ||||||||||||
125437141 | 12543714 | 9 | C | LASIX | FUROSEMIDE | 1 | 0 | ||||||||||||
125437141 | 12543714 | 10 | C | ALDACTONE | SPIRONOLACTONE | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125437141 | 12543714 | 1 | Chronic myeloid leukaemia |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125437141 | 12543714 | DS |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125437141 | 12543714 | Abdominal pain upper | |
125437141 | 12543714 | Arthralgia | |
125437141 | 12543714 | Cheilitis | |
125437141 | 12543714 | Corneal abrasion | |
125437141 | 12543714 | Corneal bleeding | |
125437141 | 12543714 | Cough | |
125437141 | 12543714 | Decreased appetite | |
125437141 | 12543714 | Diarrhoea | |
125437141 | 12543714 | Dyspnoea | |
125437141 | 12543714 | Eyelid oedema | |
125437141 | 12543714 | Fatigue | |
125437141 | 12543714 | Gait disturbance | |
125437141 | 12543714 | Headache | |
125437141 | 12543714 | Hepatic pain | |
125437141 | 12543714 | Insomnia | |
125437141 | 12543714 | Joint swelling | |
125437141 | 12543714 | Nausea | |
125437141 | 12543714 | Oral mucosal exfoliation | |
125437141 | 12543714 | Oral pain | |
125437141 | 12543714 | Pain of skin | |
125437141 | 12543714 | Periorbital oedema | |
125437141 | 12543714 | Rash | |
125437141 | 12543714 | Secretion discharge |
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 |
---|---|---|---|---|---|---|
125437141 | 12543714 | 1 | 20160608 | 20160705 | 0 |