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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126652371 | 12665237 | 1 | I | 20141125 | 20160803 | 20160818 | 20160818 | EXP | FR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-064652 | BRISTOL MYERS SQUIBB | 75.97 | YR | M | Y | 0.00000 | 20160818 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126652371 | 12665237 | 1 | PS | COUMADINE | WARFARIN SODIUM | 1 | Oral | N | 9218 | TABLET | |||||||||
| 126652371 | 12665237 | 2 | C | BISOPROLOL | BISOPROLOL | 1 | Unknown | 1 TAB, BID | U | 0 | 1 | DF | TABLET | BID | |||||
| 126652371 | 12665237 | 3 | C | DIGOXINE | DIGOXIN | 1 | Unknown | 1 TAB, QD | U | 0 | 1 | DF | QD | ||||||
| 126652371 | 12665237 | 4 | C | CORDARONE | AMIODARONE HYDROCHLORIDE | 1 | Unknown | 1 TAB, QD | U | 0 | 1 | DF | TABLET | QD | |||||
| 126652371 | 12665237 | 5 | C | SPIRIVA | TIOTROPIUM BROMIDE MONOHYDRATE | 1 | Other | 1 DF, QD | U | 0 | 1 | DF | CAPSULE | QD | |||||
| 126652371 | 12665237 | 6 | C | SERETIDE | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | Unknown | 1 DF, BID | U | 0 | 1 | DF | BID | ||||||
| 126652371 | 12665237 | 7 | C | NOCTAMIDE | LORMETAZEPAM | 1 | Unknown | 1 MG, QD | U | 0 | 1 | MG | CAPSULE | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126652371 | 12665237 | 1 | Atrial fibrillation |
| 126652371 | 12665237 | 2 | Product used for unknown indication |
| 126652371 | 12665237 | 3 | Product used for unknown indication |
| 126652371 | 12665237 | 4 | Product used for unknown indication |
| 126652371 | 12665237 | 5 | Product used for unknown indication |
| 126652371 | 12665237 | 6 | Product used for unknown indication |
| 126652371 | 12665237 | 7 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126652371 | 12665237 | HO |
| 126652371 | 12665237 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126652371 | 12665237 | Fall | |
| 126652371 | 12665237 | Haemorrhagic stroke | |
| 126652371 | 12665237 | Head injury |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |