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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6523914 | 7183525 | F | 6523914-5 | 20090601 | 20091228 | 20091231 | EXP | US-CELGENEUS-163-21880-09111207 | CELGENEUS | 77 | M | Y | 20091231 | MD | 20091010 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6523914 | 1012888034 | PS | REVLIMID | 1 | ORAL | 021880 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6523914 | 1012888034 | MULTIPLE MYELOMA |
Outcome of event
Event ID | OUTC COD |
---|---|
6523914 | DE |
6523914 | HO |
Reactions reported
Event ID | PT |
---|---|
6523914 | ABSCESS |
6523914 | CELLULITIS |
6523914 | DRUG INTOLERANCE |
6523914 | 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 |
---|---|---|---|---|---|
6523914 | 1012888034 | 20090601 | 20090101 |