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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127521391 | 12752139 | 1 | I | 20160908 | 0 | 20160915 | 20160915 | DIR | FDA-CTU | 74.52 | YR | M | N | 88.10000 | KG | 20160914 | N | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127521391 | 12752139 | 1 | PS | DEXAMETHASONE. | DEXAMETHASONE | 1 | 0 | 20 | MG | ||||||||||
| 127521391 | 12752139 | 2 | SS | LENALIDOMIDE (CC-5013) | LENALIDOMIDE | 1 | 0 | 25 | MG | ||||||||||
| 127521391 | 12752139 | 3 | SS | VELCADE | BORTEZOMIB | 1 | 0 | 2.73 | MG |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127521391 | 12752139 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127521391 | 12752139 | Back pain | |
| 127521391 | 12752139 | Heart rate irregular | |
| 127521391 | 12752139 | Peripheral swelling |
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 |
|---|---|---|---|---|---|---|
| 127521391 | 12752139 | 1 | 20160910 | 0 | ||
| 127521391 | 12752139 | 2 | 20160911 | 0 | ||
| 127521391 | 12752139 | 3 | 20160909 | 0 |