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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 121809933 | 12180993 | 3 | F | 20160202 | 20160627 | 20160315 | 20160701 | EXP | IT-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-015707 | BRISTOL MYERS SQUIBB | 84.76 | YR | F | Y | 0.00000 | 20160701 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 121809933 | 12180993 | 1 | PS | COUMADIN | WARFARIN SODIUM | 1 | Unknown | U | 9218 | TABLET | |||||||||
| 121809933 | 12180993 | 2 | C | BISOPROLOL HEMIFUMARATE | BISOPROLOL FUMARATE | 1 | Unknown | U | 0 | ||||||||||
| 121809933 | 12180993 | 3 | C | LANSOPRAZOLE. | LANSOPRAZOLE | 1 | Unknown | U | 0 | ||||||||||
| 121809933 | 12180993 | 4 | C | LORAZEPAM. | LORAZEPAM | 1 | Unknown | U | 0 | ||||||||||
| 121809933 | 12180993 | 5 | C | MEDROL | METHYLPREDNISOLONE | 1 | Unknown | U | 0 | TABLET | |||||||||
| 121809933 | 12180993 | 6 | C | ENAPREN | ENALAPRIL MALEATE | 1 | Unknown | U | 0 | TABLET | |||||||||
| 121809933 | 12180993 | 7 | C | NATECAL D3 | CALCIUM CARBONATECHOLECALCIFEROL | 1 | Unknown | U | 0 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 121809933 | 12180993 | 1 | Atrial fibrillation |
| 121809933 | 12180993 | 2 | Hypertension |
| 121809933 | 12180993 | 3 | Product used for unknown indication |
| 121809933 | 12180993 | 4 | Product used for unknown indication |
| 121809933 | 12180993 | 5 | Product used for unknown indication |
| 121809933 | 12180993 | 6 | Hypertension |
| 121809933 | 12180993 | 7 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 121809933 | 12180993 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 121809933 | 12180993 | International normalised ratio increased | |
| 121809933 | 12180993 | Vision blurred |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |