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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5327661 | 6314672 | F | 5327661-7 | 20070321 | 20070510 | 20070517 | EXP | B0470670A | GLAXOSMITHKLINE | 57 | YR | F | Y | 60 | KG | 20070517 | CN | 20070330 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5327661 | 1008489324 | PS | ARIXTRA | 1 | SUBCUTANEOUS | 7.5MG PER DAY | UNSPECIFIED | 021345 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5327661 | 1008489324 | PULMONARY EMBOLISM |
Outcome of event
Event ID | OUTC COD |
---|---|
5327661 | DE |
5327661 | LT |
Reactions reported
Event ID | PT |
---|---|
5327661 | EPISTAXIS |
5327661 | OXYGEN SATURATION DECREASED |
5327661 | PULMONARY EMBOLISM |
5327661 | THROMBOCYTOPENIA |
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 |
---|---|---|---|---|---|
5327661 | 1008489324 | 20070313 | 20070325 | 13 | DAY |