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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6810647 | 7449280 | I | 6810647-0 | 20100507 | 20100621 | 20100630 | EXP | GB-MPIJNJ-2010-03162 | MPIFDA | YR | Y | 20100630 | PH | 20100507 | UNITED KINGDOM |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6810647 | 1014009306 | PS | VELCADE | 1 | UNK | NOT REPORTED | 021602 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6810647 | 1014009306 | MULTIPLE MYELOMA |
Outcome of event
Event ID | OUTC COD |
---|---|
6810647 | DE |
Reactions reported
Event ID | PT |
---|---|
6810647 | CONDITION AGGRAVATED |
6810647 | DEATH |
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 |
---|---|---|---|---|---|
6810647 | 1014009306 | 20100427 | 20100430 | 4 | DAY |