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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5327662 | 6314673 | I | 5327662-9 | 20070201 | 20070507 | 20070517 | EXP | B0470813A | GLAXOSMITHKLINE | 31 | YR | F | Y | 20070517 | CN | FRANCE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5327662 | 1008489325 | PS | ARIXTRA | 1 | SUBCUTANEOUS | 7.5MG PER DAY | UNSPECIFIED | 021345 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5327662 | 1008489325 | HEPARIN-INDUCED THROMBOCYTOPENIA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5327662 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5327662 | ANAEMIA |
| 5327662 | HAEMATURIA |
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 |
|---|---|---|---|---|---|
| 5327662 | 1008489325 | 20070201 | 20070209 | 9 | DAY |