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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8480344 | 8644645 | I | 8480344-7 | 20120529 | 20120622 | 20120630 | PER | US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2012-BP-14304BP | B.I. PHARMACEUTICALS,INC./RIDGEFIELD | 72 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8480344 | 1020135292 | PS | PRADAXA | 1 | ORAL | 300 MG | NOT REPORTED | 022512 | |||
| 8480344 | 1020135293 | C | COQ10 | 2 | |||||||
| 8480344 | 1020135294 | C | FISH OIL | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 8480344 | 1020135292 | ATRIAL FIBRILLATION |
| 8480344 | 1020135293 | SUPPLEMENTATION THERAPY |
| 8480344 | 1020135294 | SUPPLEMENTATION THERAPY |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 8480344 | AGITATION |
| 8480344 | DEPRESSION |
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 |
|---|---|---|---|---|---|
| 8480344 | 1020135292 | 20120511 | |||
| 8480344 | 1020135293 | 20040101 | |||
| 8480344 | 1020135294 | 20020101 |