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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
8480343 | 8644644 | I | 8480343-5 | 20120622 | 20120630 | PER | US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2012-BP-14308BP | B.I. PHARMACEUTICALS,INC./RIDGEFIELD | 88 | YR | F | Y | 20120630 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
8480343 | 1020135291 | SS | PRADAXA | 1 | NOT REPORTED | 022512 | |||||
8480343 | 1020135290 | PS | PRADAXA | 1 | ORAL | 300 MG | NOT REPORTED | 022512 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
8480343 | 1020135290 | ATRIAL FIBRILLATION |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
8480343 | DIZZINESS |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |