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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4869373 | 5953266 | I | 4869373-X | 20051220 | 20051230 | EXP | 2005GB02487 | AZPRODUW00 | M | Y | 20051230 | OT | UNITED KINGDOM |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4869373 | 1006775843 | PS | IRESSA | 1 | ORAL | 021399 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4869373 | 1006775843 | OROPHARYNGEAL CANCER STAGE UNSPECIFIED |
Outcome of event
Event ID | OUTC COD |
---|---|
4869373 | DS |
4869373 | OT |
Reactions reported
Event ID | PT |
---|---|
4869373 | GASTRITIS |
4869373 | NAUSEA |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |