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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123879423 | 12387942 | 3 | F | 20160705 | 20160520 | 20160718 | EXP | US-CIPLA LTD.-2016US05463 | CIPLA | 0.00 | Y | 0.00000 | 20160718 | OT | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123879423 | 12387942 | 1 | PS | WARFARIN SODIUM. | WARFARIN SODIUM | 1 | Oral | 5 MG, QD | U | U | I1511900 | 90935 | 5 | MG | TABLET | ||||
| 123879423 | 12387942 | 2 | SS | WARFARIN SODIUM. | WARFARIN SODIUM | 1 | Unknown | UNK | U | U | 90935 | TABLET | |||||||
| 123879423 | 12387942 | 3 | C | TOPROL XL | METOPROLOL SUCCINATE | 1 | UNK, QD | U | U | 0 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123879423 | 12387942 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123879423 | 12387942 | Drug ineffective | |
| 123879423 | 12387942 | International normalised ratio abnormal |
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 |
|---|---|---|---|---|---|---|
| 123879423 | 12387942 | 1 | 20160308 | 0 |