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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5128413 | 6323469 | I | 5128413-3 | 20060901 | 20061002 | 20061011 | EXP | 163-21880-06100085 | CELGENE CORPORATION | 55 | YR | F | N | 20061002 | PH | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5128413 | 1007762974 | PS | REVLIMID | 1 | ORAL | 1 IN 1 D, ORAL | U | D | 21880 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5128413 | 1007762974 | MULTIPLE MYELOMA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5128413 | HO |
| 5128413 | RI |
Reactions reported
| Event ID | PT |
|---|---|
| 5128413 | ANAEMIA |
| 5128413 | DEHYDRATION |
| 5128413 | STOMATITIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5128413 | CSM |
| 5128413 | HP |
| 5128413 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5128413 | 1007762974 | 20060701 | 20060901 |