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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4390696 | 4167622 | I | 4390696-5 | 20040416 | 20040617 | 20040630 | EXP | 163-20785-04060133 | CELGENE CORPORATION | 65 | YR | M | N | 20040617 | CN | 20040416 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4390696 | 1004990065 | PS | THALOMID | 1 | ORAL | 50 MG, DAILY, ORAL | D | D | 20785 | ||
| 4390696 | 1005008083 | SS | DECADRON | 1 | 4 DAYS ON, 4 DAYS OFF |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4390696 | 1004990065 | MULTIPLE MYELOMA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4390696 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 4390696 | CARDIAC DISORDER |
| 4390696 | STRESS SYMPTOMS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4390696 | CSM |
| 4390696 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4390696 | 1004990065 | 20040317 | 20040101 | ||
| 4390696 | 1005008083 | 20040101 |