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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5327663 | 6314674 | I | 5327663-0 | 20070301 | 20070507 | 20070517 | EXP | B0470832A | GLAXOSMITHKLINE | 52 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5327663 | 1008489326 | PS | ARIXTRA | 1 | SUBCUTANEOUS | 2.5MG PER DAY | UNSPECIFIED | 021345 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5327663 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5327663 | DRUG INEFFECTIVE |
| 5327663 | DYSPNOEA |
| 5327663 | HYPOCAPNIA |
| 5327663 | PAIN IN EXTREMITY |
| 5327663 | PULMONARY EMBOLISM |
| 5327663 | THROMBOSIS |
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 |
|---|---|---|---|---|---|
| 5327663 | 1008489326 | 20070308 | 20070315 | 8 | DAY |