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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5472350 | 6431115 | I | 5472350-1 | 20070806 | 20070918 | 20070930 | EXP | US-SHR-US-2007-035174 | BERLEX | 55 | YR | F | Y | 61.224 | KG | 20070928 | OT | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5472350 | 1008989640 | PS | LEUKINE | 1 | SUBCUTANEOUS | 400 MCG | |||||
| 5472350 | 1008989641 | SS | LEUKINE | 1 | SUBCUTANEOUS | 400 MCG | |||||
| 5472350 | 1008989642 | C | CARBOPLATIN | 1 | INTRAVENOUS | 460 UNK, UNK | |||||
| 5472350 | 1008989643 | C | HERCEPTIN | 1 | INTRAVENOUS | 50 MG, UNK | |||||
| 5472350 | 1008989644 | C | EMEND | 1 | ORAL | ||||||
| 5472350 | 1008989645 | C | DECADRON /CAN/ | 2 | 4 MG, 2X/DAY | ||||||
| 5472350 | 1008989646 | C | KYTRIL | 1 | 1 MG, 2X/DAY | ||||||
| 5472350 | 1008989647 | C | TAXOTERE | 1 | 120 MG |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5472350 | 1008989640 | BREAST CANCER |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5472350 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5472350 | DISORIENTATION |
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 |
|---|---|---|---|---|---|
| 5472350 | 1008989640 | 20070710 | 20070713 | 4320 | MIN |
| 5472350 | 1008989641 | 20070731 | 20070803 | 4320 | MIN |
| 5472350 | 1008989647 | 20070709 | 20070730 | 30240 | MIN |