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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 121778674 | 12177867 | 4 | F | 20160228 | 20160624 | 20160315 | 20160706 | EXP | IT-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-015701 | BRISTOL MYERS SQUIBB | 80.11 | YR | F | Y | 0.00000 | 20160706 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 121778674 | 12177867 | 1 | PS | COUMADIN | WARFARIN SODIUM | 1 | Oral | 5 MG, PRN | Y | 9218 | 5 | MG | TABLET | ||||||
| 121778674 | 12177867 | 2 | SS | SOTALOL. | SOTALOL | 1 | Oral | 200 MG, QD | Y | 0 | 200 | MG | QD | ||||||
| 121778674 | 12177867 | 3 | C | AMLODIPINE BESILATE | AMLODIPINE BESYLATE | 1 | Oral | 10 MG, UNK | U | 0 | 10 | MG | |||||||
| 121778674 | 12177867 | 4 | C | RAMIPRIL. | RAMIPRIL | 1 | Oral | 5 U, UNK | U | 0 | 5 | DF | |||||||
| 121778674 | 12177867 | 5 | C | PANTOPRAZOLE | PANTOPRAZOLE SODIUM | 1 | Oral | 20 MG, UNK | U | 0 | 20 | MG | |||||||
| 121778674 | 12177867 | 6 | C | DIBASE | CHOLECALCIFEROL | 1 | Oral | 1 UNK, UNK | U | 0 | 1 | DF |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 121778674 | 12177867 | 1 | Atrial fibrillation |
| 121778674 | 12177867 | 2 | Atrial fibrillation |
| 121778674 | 12177867 | 3 | Hypertension |
| 121778674 | 12177867 | 4 | Hypertension |
| 121778674 | 12177867 | 5 | Product used for unknown indication |
| 121778674 | 12177867 | 6 | Vitamin D deficiency |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 121778674 | 12177867 | HO |
| 121778674 | 12177867 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 121778674 | 12177867 | Bradycardia | |
| 121778674 | 12177867 | Fall | |
| 121778674 | 12177867 | Overdose | |
| 121778674 | 12177867 | Pancreatitis | |
| 121778674 | 12177867 | Subarachnoid haemorrhage | |
| 121778674 | 12177867 | Syncope |
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 |
|---|---|---|---|---|---|---|
| 121778674 | 12177867 | 1 | 20160227 | 0 |