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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4303922 | 4100782 | I | 4303922-5 | 20031201 | 20040211 | 20040223 | EXP | 163-20785-04020338 | CELGENE CORPORATION | 69 | YR | M | N | 20040212 | 20031226 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4303922 | 1004651295 | PS | THALOMID | 1 | ORAL | 200 MG, DAILY, ORAL | D | D | 20785 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4303922 | 1004651295 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4303922 | DE |
| 4303922 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4303922 | AMMONIA INCREASED |
| 4303922 | COMA |
| 4303922 | ENCEPHALOPATHY |
| 4303922 | MULTIPLE MYELOMA |
| 4303922 | PNEUMONIA ASPIRATION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4303922 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4303922 | 1004651295 | 1 | YR |