Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8480345 | 8644646 | I | 8480345-9 | 20120622 | 20120622 | 20120630 | PER | US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2012-BP-14294BP | B.I. PHARMACEUTICALS,INC./RIDGEFIELD | 85 | YR | M | Y | 20120630 | CN | UNITED STATES |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8480345 | 1020135295 | PS | PRADAXA | 1 | ORAL | 300 MG | NOT REPORTED | 022512 | |||
| 8480345 | 1020135296 | C | DILTIAZEM HYDROCHOLORIDE | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 8480345 | 1020135295 | ATRIAL FIBRILLATION |
| 8480345 | 1020135296 | HYPERTENSION |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 8480345 | DYSPHAGIA |
| 8480345 | HEMIPARESIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |