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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7387024 | 7880272 | I | 7387024-X | 20110314 | 20110318 | 20110331 | EXP | DE-CELGENEUS-062-C5013-11032311 | CELGENEUS | 55 | YR | M | Y | 97 | KG | 20110331 | OT | GERMANY |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7387024 | 1016140034 | SS | LENALIDOMIDE | 1 | ORAL | ||||||
| 7387024 | 1016140033 | PS | LENALIDOMIDE | 1 | ORAL | 021880 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7387024 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 7387024 | CARDIOVASCULAR FUNCTION TEST |
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 |
|---|---|---|---|---|---|
| 7387024 | 1016140034 | 20110309 | |||
| 7387024 | 1016140033 | 20100128 |