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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7789543 | 8131175 | F | 7789543-0 | 20110801 | 20110920 | 20110930 | PER | US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2011-BP-21030BP | B.I. PHARMACEUTICALS,INC./RIDGEFIELD | 66 | YR | F | Y | 20110930 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7789543 | 1017679348 | C | ZOCOR | 1 | ORAL | ||||||
| 7789543 | 1017679349 | C | CALCIUM CARBONATE | 1 | ORAL | ||||||
| 7789543 | 1017679347 | C | METOPROLOL | 2 | ORAL | 50 MG | |||||
| 7789543 | 1017679346 | PS | PRADAXA | 1 | ORAL | 300 MG | NOTREPORTED | 022512 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7789543 | 1017679348 | BLOOD CHOLESTEROL INCREASED |
| 7789543 | 1017679349 | SUPPLEMENTATION THERAPY |
| 7789543 | 1017679347 | ATRIAL FIBRILLATION |
| 7789543 | 1017679346 | ATRIAL FIBRILLATION |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 7789543 | DARK CIRCLES UNDER EYES |
| 7789543 | ERYTHEMA OF EYELID |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 7789543 | 1017679346 | 20110611 |