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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5293128 | 6105285 | F | 1 | 5293128-8 | 20060701 | 20070329 | 20070404 | EXP | 163-21880-06070753 | CELGENE CORPORATION | M | N | 20070329 | OT | 20060701 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5293128 | 1008354735 | PS | REVLIMID | 1 | ORAL | SEE IMAGE | D | D | 21880 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5293128 | 1008354735 | MYELODYSPLASTIC SYNDROME |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5293128 | DE |
| 5293128 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5293128 | DYSPNOEA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5293128 | CR |
| 5293128 | HP |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5293128 | 1008354735 | 20060701 | |||
| 5293128 | 1008354735 | 20060101 |