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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125316361 | 12531636 | 1 | I | 20150215 | 20150629 | 20160706 | 20160706 | EXP | PL-CELGENEUS-POL-2015070868 | CELGENE | 66.28 | YR | F | Y | 0.00000 | 20160706 | OT | PL | PL |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125316361 | 12531636 | 1 | PS | REVLIMID | LENALIDOMIDE | 1 | Oral | Y | U | 21880 | CAPSULES | ||||||||
| 125316361 | 12531636 | 2 | SS | DEXAMETHASONE. | DEXAMETHASONE | 1 | Unknown | Y | U | 0 | UNKNOWN |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125316361 | 12531636 | 1 | Plasma cell myeloma |
| 125316361 | 12531636 | 2 | Plasma cell myeloma |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125316361 | 12531636 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125316361 | 12531636 | Abscess limb | |
| 125316361 | 12531636 | Anaemia | |
| 125316361 | 12531636 | Bronchitis | |
| 125316361 | 12531636 | Haemorrhagic disorder | |
| 125316361 | 12531636 | Pharyngitis | |
| 125316361 | 12531636 | Respiratory tract infection | |
| 125316361 | 12531636 | Upper respiratory tract infection |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |