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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4390693 | 4157613 | F | 1 | 4390693-X | 20040101 | 20040617 | 20040630 | EXP | 163-20785-04040580 | CELGENE CORPORATION | 74 | YR | F | N | 107.3 | LBS | 20040617 | MD | 20040517 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4390693 | 1004990062 | PS | THALOMID | 1 | ORAL | 200 MG , DAILY , ORAL | D | D | 20785 | ||
| 4390693 | 1005007996 | C | DECADRON | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4390693 | 1004990062 | MULTIPLE MYELOMA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4390693 | DE |
| 4390693 | OT |
| 4390693 | RI |
Reactions reported
| Event ID | PT |
|---|---|
| 4390693 | CONVULSION |
| 4390693 | DERMATITIS |
| 4390693 | IMPAIRED HEALING |
| 4390693 | MALIGNANT NEOPLASM PROGRESSION |
| 4390693 | MULTIPLE MYELOMA |
| 4390693 | PANCYTOPENIA |
| 4390693 | PYREXIA |
| 4390693 | RASH |
| 4390693 | RENAL FAILURE |
| 4390693 | STOMATITIS |
| 4390693 | WEIGHT DECREASED |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4390693 | CSM |
| 4390693 | HP |
| 4390693 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4390693 | 1004990062 | 13 | DAY |