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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5903469 | 6775416 | I | 5903469-6 | 20080728 | 20080919 | 20080930 | EXP | CN-BAXTER-2008BH009864 | BAXTER | 14 | YR | M | Y | 42 | KG | 20080930 | MD | CHINA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5903469 | 1010520625 | PS | RECOMBINATE | 1 | INTRAVENOUS | UNKNOWN |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5903469 | 1010520625 | FACTOR VIII DEFICIENCY |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5903469 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5903469 | HAEMORRHAGE |
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 |
|---|---|---|---|---|---|
| 5903469 | 1010520625 | 20080728 | 20080801 |