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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 94730403 | 9473040 | 3 | F | 20160728 | 20130823 | 20160804 | EXP | US-BRISTOL-MYERS SQUIBB COMPANY-17359282 | BRISTOL MYERS SQUIBB | 0.00 | M | Y | 84.80000 | KG | 20160804 | CN | US | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 94730403 | 9473040 | 1 | PS | SPRYCEL | DASATINIB | 1 | Oral | REDUCED:80MG EVERY OTHER DAY:03FEB2013 | Y | U | 1E6048E | 21986 | 70 | MG | FILM-COATED TABLET | QD | |||
| 94730403 | 9473040 | 2 | SS | TYLENOL PM | ACETAMINOPHENDIPHENHYDRAMINE | 1 | Unknown | U | 0 | ||||||||||
| 94730403 | 9473040 | 3 | C | FLECAINIDE | FLECAINIDE | 1 | Unknown | UNK UNK, BID | U | 0 | 100 | MG | BID | ||||||
| 94730403 | 9473040 | 4 | C | AVODART | DUTASTERIDE | 1 | Unknown | .5 MG, QD | U | 0 | .5 | MG | QD | ||||||
| 94730403 | 9473040 | 5 | C | TAMSULOSIN | TAMSULOSIN | 1 | Unknown | .4 MG, UNK | U | 0 | .4 | MG | |||||||
| 94730403 | 9473040 | 6 | C | DILTIAZEM HCL | DILTIAZEM HYDROCHLORIDE | 1 | Unknown | 120 MG, QD | U | 0 | 120 | MG | QD | ||||||
| 94730403 | 9473040 | 7 | C | ALLOPURINOL. | ALLOPURINOL | 1 | Unknown | 100 MG, QD | U | 0 | 100 | MG | QD | ||||||
| 94730403 | 9473040 | 8 | C | FLUTICASONE | FLUTICASONEFLUTICASONE PROPIONATE | 1 | Unknown | U | 0 | ||||||||||
| 94730403 | 9473040 | 9 | C | FUROSEMIDE. | FUROSEMIDE | 1 | Unknown | 40 MG, UNK | U | 0 | 40 | MG | |||||||
| 94730403 | 9473040 | 10 | C | ALDACTONE | SPIRONOLACTONE | 1 | Unknown | 25 MG, UNK | U | 0 | 25 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 94730403 | 9473040 | 1 | Chronic myeloid leukaemia |
| 94730403 | 9473040 | 2 | Product used for unknown indication |
| 94730403 | 9473040 | 3 | Atrial fibrillation |
| 94730403 | 9473040 | 4 | Prostatic disorder |
| 94730403 | 9473040 | 5 | Drug therapy |
| 94730403 | 9473040 | 6 | Product used for unknown indication |
| 94730403 | 9473040 | 7 | Blood uric acid |
| 94730403 | 9473040 | 8 | Product used for unknown indication |
| 94730403 | 9473040 | 9 | Product used for unknown indication |
| 94730403 | 9473040 | 10 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 94730403 | 9473040 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 94730403 | 9473040 | Blood uric acid abnormal | |
| 94730403 | 9473040 | Fatigue | |
| 94730403 | 9473040 | Hepatic enzyme increased | |
| 94730403 | 9473040 | Hypertension | |
| 94730403 | 9473040 | Platelet count decreased | |
| 94730403 | 9473040 | Pleural effusion | |
| 94730403 | 9473040 | White blood cell count decreased |
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 |
|---|---|---|---|---|---|---|
| 94730403 | 9473040 | 1 | 20130207 | 0 |