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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126466011 | 12646601 | 1 | I | 20160728 | 20160801 | 20160812 | 20160812 | EXP | IT-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-063456 | BRISTOL MYERS SQUIBB | 84.03 | YR | F | Y | 0.00000 | 20160812 | CN | IT | IT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126466011 | 12646601 | 1 | PS | COUMADIN | WARFARIN SODIUM | 1 | Oral | 1 U, QD | Y | 9218 | 1 | DF | TABLET | QD | |||||
| 126466011 | 12646601 | 2 | SS | ZOLOFT | SERTRALINE HYDROCHLORIDE | 1 | Oral | 1 U, QD | U | 0 | 1 | DF | QD | ||||||
| 126466011 | 12646601 | 3 | SS | TAVOR (LORAZEPAM) | LORAZEPAM | 1 | Oral | 1 U, QD | U | 0 | 1 | DF | QD | ||||||
| 126466011 | 12646601 | 4 | SS | CONGESCOR | BISOPROLOL | 1 | Oral | 1 U, QD | U | 0 | 1 | DF | QD | ||||||
| 126466011 | 12646601 | 5 | SS | luvion | CANRENONE | 1 | Oral | 50 MG, QD | U | 0 | 50 | MG | QD | ||||||
| 126466011 | 12646601 | 6 | SS | LASIX | FUROSEMIDE | 1 | Oral | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126466011 | 12646601 | 1 | Atrial fibrillation |
| 126466011 | 12646601 | 2 | Depression |
| 126466011 | 12646601 | 3 | Hypertension |
| 126466011 | 12646601 | 4 | Hypertension |
| 126466011 | 12646601 | 5 | Hypertension |
| 126466011 | 12646601 | 6 | Hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126466011 | 12646601 | OT |
| 126466011 | 12646601 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126466011 | 12646601 | Cerebral haemorrhage | |
| 126466011 | 12646601 | Fall |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |