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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5120034 | 6093009 | F | 1 | 5120034-1 | 20060628 | 20060919 | 20060929 | EXP | 2006083824 | PFIZER INC | 72 | YR | M | N | 60 | KG | 20060928 | MD | FRANCE |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5120034 | 1007726848 | PS | SUTENT | 1 | U | U | 21938 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
5120034 | HO |
Reactions reported
Event ID | PT |
---|---|
5120034 | PANCYTOPENIA |
5120034 | UNEVALUABLE EVENT |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
5120034 | FGN |
5120034 | HP |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
5120034 | 1007726848 | 20060609 |