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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123410282 | 12341028 | 2 | F | 20160424 | 20160823 | 20160506 | 20160825 | PER | US-TAKEDA-2016MPI003567 | TAKEDA | 72.08 | YR | M | Y | 0.00000 | 20160825 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123410282 | 12341028 | 1 | PS | NINLARO | IXAZOMIB | 1 | Oral | 4 MG, UNK | 1402447 | 208462 | 4 | MG | CAPSULE | /wk | |||||
| 123410282 | 12341028 | 2 | SS | DEXAMETHASONE. | DEXAMETHASONE | 1 | Unknown | 40 MG, UNK | 0 | 40 | MG | ||||||||
| 123410282 | 12341028 | 3 | C | REVLIMID | LENALIDOMIDE | 1 | Unknown | 10 MG, UNK | U | 0 | 10 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123410282 | 12341028 | 1 | Plasma cell myeloma |
| 123410282 | 12341028 | 2 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123410282 | 12341028 | Dyspnoea | |
| 123410282 | 12341028 | Localised oedema | |
| 123410282 | 12341028 | Nausea | |
| 123410282 | 12341028 | Oedema peripheral |
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 |
|---|---|---|---|---|---|---|
| 123410282 | 12341028 | 1 | 20160414 | 0 |