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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126584142 | 12658414 | 2 | F | 201603 | 20160811 | 20160817 | 20160823 | EXP | FR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-064622 | BRISTOL MYERS SQUIBB | 77.00 | YR | M | Y | 0.00000 | 20160823 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126584142 | 12658414 | 1 | PS | COUMADINE | WARFARIN SODIUM | 1 | Oral | 5 MG, QD | Y | 9218 | 5 | MG | TABLET | QD | |||||
| 126584142 | 12658414 | 2 | SS | COUMADINE | WARFARIN SODIUM | 1 | Unknown | 2 MG, UNK, 2 MG, 1.5 OF A TABLET | Y | 9218 | 2 | MG | TABLET | QD | |||||
| 126584142 | 12658414 | 3 | C | JANUMET | METFORMIN HYDROCHLORIDESITAGLIPTIN PHOSPHATE | 1 | Unknown | 1 DF, UNK | U | 0 | 1 | DF | |||||||
| 126584142 | 12658414 | 4 | C | BISOCE | BISOPROLOL | 1 | Unknown | U | 0 | ||||||||||
| 126584142 | 12658414 | 5 | C | COAPROVEL | HYDROCHLOROTHIAZIDEIRBESARTAN | 1 | Unknown | 1 DF, UNK | U | 0 | 1 | DF | |||||||
| 126584142 | 12658414 | 6 | C | TAHOR | ATORVASTATIN CALCIUM | 1 | Unknown | U | 0 | ||||||||||
| 126584142 | 12658414 | 7 | C | XATRAL | ALFUZOSIN | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126584142 | 12658414 | 1 | Arrhythmia prophylaxis |
| 126584142 | 12658414 | 3 | Product used for unknown indication |
| 126584142 | 12658414 | 4 | Product used for unknown indication |
| 126584142 | 12658414 | 5 | Product used for unknown indication |
| 126584142 | 12658414 | 6 | Product used for unknown indication |
| 126584142 | 12658414 | 7 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126584142 | 12658414 | OT |
| 126584142 | 12658414 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126584142 | 12658414 | Acute kidney injury | |
| 126584142 | 12658414 | International normalised ratio increased | |
| 126584142 | 12658414 | Overdose |
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 |
|---|---|---|---|---|---|---|
| 126584142 | 12658414 | 1 | 2012 | 0 |