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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6661984 | 7339717 | F | 6661984-4 | 20091124 | 20100331 | PER | US-BRISTOL-MYERS SQUIBB COMPANY-14862585 | BRISTOL-MYERS SQUIBB COMPANY | 47 | YR | M | Y | 20100325 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6661984 | 1013422829 | PS | ERBITUX | 1 | RECEIVED 1ST DOSE | ||||||
| 6661984 | 1013422830 | C | STEROIDS | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6661984 | 1013422829 | RECTAL CANCER |
| 6661984 | 1013422830 | PREMEDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6661984 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6661984 | ANAPHYLACTIC REACTION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |