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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6250623 | 7007655 | F | 6250623-2 | 20090501 | 20090616 | 20090630 | EXP | AU-AMGEN-QUU348631 | AMGENSAFETY | 67 | F | Y | 92.05 | KG | 20090630 | MD | AUSTRALIA |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6250623 | 1011812007 | PS | NEULASTA | 1 | SUBCUTANEOUS | NOT PROVIDED | |||||
6250623 | 1011812008 | C | FLUOROURACIL | 2 | |||||||
6250623 | 1011812009 | C | EPIRUBICIN | 1 | |||||||
6250623 | 1011812010 | C | CYCLOPHOSPHAMIDE | 2 | |||||||
6250623 | 1011812011 | C | DOCETAXEL | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6250623 | 1011812007 | CHEMOTHERAPY |
Outcome of event
Event ID | OUTC COD |
---|---|
6250623 | OT |
Reactions reported
Event ID | PT |
---|---|
6250623 | FEBRILE NEUTROPENIA |
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 |
---|---|---|---|---|---|
6250623 | 1011812007 | 20090506 | |||
6250623 | 1011812008 | 20090505 | |||
6250623 | 1011812009 | 20090505 | |||
6250623 | 1011812010 | 20090505 |