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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5795297 | 6687045 | I | 5795297-X | 20080619 | 20080630 | EXP | BE-PFIZER INC-2008051915 | PFIZER INC | M | Y | 20080630 | MD | BELGIUM |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5795297 | 1010111654 | PS | SUTENT | 1 | ORAL | 21938 | |||||
| 5795297 | 1010111655 | SS | ACE INHIBITOR NOS | 2 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5795297 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5795297 | ANGIOEDEMA |
| 5795297 | HYPERTENSION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |