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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126085401 | 12608540 | 1 | I | 20160505 | 20160718 | 20160729 | 20160729 | EXP | FR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-059961 | BRISTOL MYERS SQUIBB | 80.75 | YR | F | Y | 0.00000 | 20160729 | CN | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126085401 | 12608540 | 1 | PS | COUMADINE | WARFARIN SODIUM | 1 | Oral | UNK, QD | U | 9218 | TABLET | QD | |||||||
| 126085401 | 12608540 | 2 | SS | COLCHICINE. | COLCHICINE | 1 | Oral | 0.5 MG, QD | 16 | MG | Y | 0 | .5 | MG | QD | ||||
| 126085401 | 12608540 | 3 | SS | ALLOPURINOL /00003302/ | ALLOPURINOL | 1 | Oral | UNK, QD | U | 0 | QD | ||||||||
| 126085401 | 12608540 | 4 | SS | CORDARONE | AMIODARONE HYDROCHLORIDE | 1 | Oral | 200 MG, QD | U | 0 | 200 | MG | QD | ||||||
| 126085401 | 12608540 | 5 | SS | EUPANTOL | PANTOPRAZOLE SODIUM | 1 | Oral | 40 MG, QD | U | 0 | 40 | MG | QD | ||||||
| 126085401 | 12608540 | 6 | C | TEMERIT | NEBIVOLOL | 1 | Unknown | 5 MG, UNK | U | 0 | 5 | MG | |||||||
| 126085401 | 12608540 | 7 | C | TEMESTA /00273201/ | LORAZEPAM | 1 | Unknown | 1 MG, BID | U | 0 | 1 | MG | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126085401 | 12608540 | 1 | Atrial fibrillation |
| 126085401 | 12608540 | 2 | Gout |
| 126085401 | 12608540 | 3 | Gout |
| 126085401 | 12608540 | 4 | Atrial fibrillation |
| 126085401 | 12608540 | 5 | Product used for unknown indication |
| 126085401 | 12608540 | 6 | Product used for unknown indication |
| 126085401 | 12608540 | 7 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126085401 | 12608540 | HO |
| 126085401 | 12608540 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126085401 | 12608540 | Arthritis | |
| 126085401 | 12608540 | International normalised ratio increased |
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 |
|---|---|---|---|---|---|---|
| 126085401 | 12608540 | 1 | 20160328 | 20160507 | 0 | |
| 126085401 | 12608540 | 2 | 20160404 | 20160509 | 0 | |
| 126085401 | 12608540 | 3 | 20160425 | 0 |