Person who experienced the adverse event (patient)
Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127882871 | 12788287 | 1 | I | 20140918 | 20160922 | 20160928 | 20160928 | PER | US-CELGENEUS-USA-2016095809 | CELGENE | 74.12 | YR | Y | 0.00000 | 20160928 | OT | US | US |
Drug(s) used by person
Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127882871 | 12788287 | 1 | PS | REVLIMID | LENALIDOMIDE | 1 | Oral | U | 21880 | 25 | MG | CAPSULES | /wk | ||||||
127882871 | 12788287 | 2 | SS | REVLIMID | LENALIDOMIDE | 1 | Oral | 20 | U | 21880 | 15 | MG | CAPSULES | /wk | |||||
127882871 | 12788287 | 3 | SS | REVLIMID | LENALIDOMIDE | 1 | Oral | U | 21880 | 5 | MG | CAPSULES | |||||||
127882871 | 12788287 | 4 | SS | VELCADE | BORTEZOMIB | 1 | Subcutaneous | U | 66188 | INJECTION | /wk | ||||||||
127882871 | 12788287 | 5 | SS | VELCADE | BORTEZOMIB | 1 | Subcutaneous | U | 66188 | INJECTION | /wk | ||||||||
127882871 | 12788287 | 6 | SS | DECADRON | DEXAMETHASONE | 1 | Oral | U | 0 | UNKNOWN | |||||||||
127882871 | 12788287 | 7 | SS | ZOMETA | ZOLEDRONIC ACID | 1 | Intravenous drip | 4 MILLIGRAM | U | 0 | 4 | MG | INJECTION |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127882871 | 12788287 | 1 | Plasma cell myeloma |
127882871 | 12788287 | 4 | Plasma cell myeloma |
127882871 | 12788287 | 6 | Plasma cell myeloma |
127882871 | 12788287 | 7 | Plasma cell myeloma |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127882871 | 12788287 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127882871 | 12788287 | Nausea | |
127882871 | 12788287 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
127882871 | 12788287 | 1 | 20140627 | 20141024 | 0 | |
127882871 | 12788287 | 2 | 20140627 | 20141024 | 0 | |
127882871 | 12788287 | 3 | 20140620 | 20150201 | 0 | |
127882871 | 12788287 | 4 | 20010808 | 20141024 | 0 | |
127882871 | 12788287 | 5 | 20140627 | 20140808 | 0 | |
127882871 | 12788287 | 6 | 20140627 | 20141024 | 0 | |
127882871 | 12788287 | 7 | 20140618 | 20150220 | 0 |