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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7789542 | 8163762 | I | 7789542-9 | 20110923 | 20110930 | EXP | AU-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2011-AU-01540AU | B.I. PHARMACEUTICALS,INC./RIDGEFIELD | YR | M | Y | 20110930 | MD | AUSTRALIA |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7789542 | 1017679345 | PS | PRADAXA | 1 | 022512 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
7789542 | HO |
Reactions reported
Event ID | PT |
---|---|
7789542 | ISCHAEMIC STROKE |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |