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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7029107 | 7912965 | F | 7029107-X | 20100713 | 20101003 | 20101005 | EXP | Z0005857A | GLAXOSMITHKLINE | 48 | YR | F | Y | 61 | KG | 20101005 | MD | POLAND |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7029107 | 1014836530 | PS | LAPATINIB | 2 | ORAL | 1250MG PER DAY | 022059 | ||||
| 7029107 | 1014836532 | C | LETROX | 2 | ORAL | 50MG PER DAY | |||||
| 7029107 | 1014836531 | SS | CAPECITABINE | 1 | ORAL | 2000MGM2 CYCLIC | |||||
| 7029107 | 1014836533 | C | NIMESIL | 2 | ORAL | 100MG UNKNOWN |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7029107 | 1014836532 | HYPERTHYROIDISM |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7029107 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 7029107 | 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 |
|---|---|---|---|---|---|
| 7029107 | 1014836530 | 20100615 | |||
| 7029107 | 1014836532 | 20070101 | |||
| 7029107 | 1014836531 | 20100615 | |||
| 7029107 | 1014836533 | 20100615 | 20100601 |