Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124638982 | 12463898 | 2 | F | 20160704 | 20160614 | 20160708 | EXP | PHHY2016PL079123 | NOVARTIS | 58.00 | YR | F | Y | 0.00000 | 20160708 | OT | PL | PL |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124638982 | 12463898 | 1 | PS | LAPATINIB | LAPATINIB | 1 | Unknown | UNK | 22059 | ||||||||||
| 124638982 | 12463898 | 2 | SS | CAPECITABINE. | CAPECITABINE | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124638982 | 12463898 | 1 | Breast cancer |
| 124638982 | 12463898 | 2 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124638982 | 12463898 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124638982 | 12463898 | Breast cancer | |
| 124638982 | 12463898 | Malignant neoplasm progression | |
| 124638982 | 12463898 | Nausea | |
| 124638982 | 12463898 | Paresis |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 124638982 | 12463898 | 1 | 20140703 | 20160111 | 0 | |
| 124638982 | 12463898 | 2 | 20140703 | 20160111 | 0 |