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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6734211 | 7366493 | F | 6734211-7 | 20100417 | 20100517 | 20100520 | EXP | US-CELGENEUS-163-21880-10041604 | CELGENEUS | 44 | YR | M | Y | 20100520 | MD | 20100417 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6734211 | 1013723052 | PS | REVLIMID | 1 | ORAL | 021880 | |||||
| 6734211 | 1013723053 | SS | REVLIMID | 1 | ORAL | 021880 | |||||
| 6734211 | 1013723054 | SS | REVLIMID | 1 | ORAL | 10-25MG |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6734211 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 6734211 | MULTIPLE MYELOMA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6734211 | 1013723052 | 20100201 | |||
| 6734211 | 1013723053 | 20090301 | |||
| 6734211 | 1013723054 | 20060801 |