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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125732341 | 12573234 | 1 | I | 20160525 | 20160720 | 20160720 | EXP | JP-SUN PHARMACEUTICAL INDUSTRIES LTD-2016R1-120390 | RANBAXY | 70.00 | YR | F | Y | 0.00000 | 20160720 | OT | GB | JP |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125732341 | 12573234 | 1 | SS | Bortezomib | BORTEZOMIB | 1 | Unknown | UNK | Y | 0 | |||||||||
| 125732341 | 12573234 | 2 | PS | DEXAMETHASONE. | DEXAMETHASONE | 1 | Unknown | 20 MG/KG, BODY WEIGHT | Y | 84764 | |||||||||
| 125732341 | 12573234 | 3 | SS | CYCLOPHOSPHAMIDE. | CYCLOPHOSPHAMIDE | 1 | Unknown | UNK | Y | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125732341 | 12573234 | 1 | Light chain disease |
| 125732341 | 12573234 | 2 | Light chain disease |
| 125732341 | 12573234 | 3 | Light chain disease |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125732341 | 12573234 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125732341 | 12573234 | Drug ineffective | |
| 125732341 | 12573234 | Hepatotoxicity |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |