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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5039983 | 6075130 | I | 5039983-8 | 20060622 | 20060623 | 20060630 | EXP | 2006UW13316 | AZPRODUW00 | 41 | YR | F | Y | 46.1 | KG | 20060630 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5039983 | 1007429045 | PS | IRESSA | 1 | ORAL | 21399 | |||||
5039983 | 1007429046 | SS | CAPECITABINE | 2 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5039983 | 1007429045 | BREAST CANCER METASTATIC |
5039983 | 1007429046 | BREAST CANCER METASTATIC |
Outcome of event
Event ID | OUTC COD |
---|---|
5039983 | HO |
Reactions reported
Event ID | PT |
---|---|
5039983 | PANCREATITIS ACUTE |
5039983 | URINARY TRACT INFECTION |
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 |
---|---|---|---|---|---|
5039983 | 1007429045 | 20050819 | 20060618 | 304 | DAY |
5039983 | 1007429046 | 20050819 | 20060618 | 304 | DAY |