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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
8477394 | 8642799 | I | 8477394-3 | 20120620 | 20120629 | EXP | JP-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2012-EU-03257GD | B.I. PHARMACEUTICALS,INC./RIDGEFIELD | 64 | YR | M | Y | 20120629 | OT | JAPAN |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
8477394 | 1020122579 | PS | DABIGATRAN | 2 | 022512 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
8477394 | 1020122579 | ATRIAL FIBRILLATION |
Outcome of event
Event ID | OUTC COD |
---|---|
8477394 | OT |
Reactions reported
Event ID | PT |
---|---|
8477394 | RENAL DISORDER |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |