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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125312521 | 12531252 | 1 | I | 20160629 | 20160706 | 20160706 | EXP | MX-TAKEDA-2016MPI006096 | TAKEDA | 0.00 | Y | 0.00000 | 20160706 | CN | MX | MX |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125312521 | 12531252 | 1 | PS | VELCADE | BORTEZOMIB | 1 | Unknown | UNK | 21602 | INJECTION |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125312521 | 12531252 | 1 | Unevaluable event |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125312521 | 12531252 | DE |
125312521 | 12531252 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125312521 | 12531252 | Abdominal distension | |
125312521 | 12531252 | Ataxia telangiectasia | |
125312521 | 12531252 | Constipation | |
125312521 | 12531252 | Death | |
125312521 | 12531252 | Diarrhoea | |
125312521 | 12531252 | Herpes zoster | |
125312521 | 12531252 | Myocardial infarction | |
125312521 | 12531252 | Nausea | |
125312521 | 12531252 | Neuropathy peripheral | |
125312521 | 12531252 | Pneumonia | |
125312521 | 12531252 | Thrombocytopenia | |
125312521 | 12531252 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |