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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6138272 | 6956711 | I | 6138272-8 | 20081101 | 20090320 | 20090331 | EXP | B0567085A | GLAXOSMITHKLINE | F | Y | 70 | KG | 20090331 | MD | SWITZERLAND |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6138272 | 1011356965 | PS | ARIXTRA | 1 | SUBCUTANEOUS | 2.5MG PER DAY | 021345 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6138272 | 1011356965 | THROMBOSIS PROPHYLAXIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6138272 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6138272 | DRUG INEFFECTIVE |
| 6138272 | PULMONARY EMBOLISM |
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 |
|---|---|---|---|---|---|
| 6138272 | 1011356965 | 20080101 |