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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125554311 | 12555431 | 1 | I | 20160629 | 20160714 | 20160714 | EXP | US-CIPLA LTD.-2016US09548 | CIPLA | WAGNER L, TURPIN B, NAGARAJAN R, WEISS B, CRIPE T, GELLER J. PILOT STUDY OF VINCRISTINE, ORAL IRINOTECAN, AND TEMOZOLOMIDE (VOIT REGIMEN) COMBINED WITH BEVACIZUMAB IN PEDIATRIC PATIENTS WITH RECURRENT SOLID TUMORS OR BRAIN TUMORS. PEDIATR BLOOD CANCER. 2013;60:1447 TO 1457 | 0.00 | Y | 0.00000 | 20160714 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125554311 | 12555431 | 1 | PS | Irinotecan | IRINOTECAN | 1 | Oral | 90 MG/M2, ON DAYS 1-5 IN 3 WEEKS | U | 77219 | 90 | MG/M**2 | |||||||
125554311 | 12555431 | 2 | SS | Vincristine | VINCRISTINE | 1 | Intravenous (not otherwise specified) | 1.5 MG/M2, OVER 1 MINUTE ON DAY 1, EVERY 3 WEEK CYCLE | U | 0 | 1.5 | MG/M**2 | |||||||
125554311 | 12555431 | 3 | SS | TEMOZOLOMIDE. | TEMOZOLOMIDE | 1 | Oral | 150 MG/M2/DAY ON DAYS 1TO 5, EVERY 3 WEEK CYCLE | U | 0 | 150 | MG/M**2 | CAPSULE | ||||||
125554311 | 12555431 | 4 | SS | Bevacizumab | BEVACIZUMAB | 1 | Unknown | 15 MG/KG, OVER 90 MINUTES ON DAY 1, EVERY 3 WEEK CYCLE | U | 0 | 15 | MG/KG | |||||||
125554311 | 12555431 | 5 | C | CEFIXIME. | CEFIXIME | 1 | Unknown | 8 MG/KG DAILY, 10 DAYS STARTING 2 DAYS BEFORE EACH CHEMOTHERAPY CYCLE | U | U | 0 | 8 | MG/KG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125554311 | 12555431 | 1 | Nephroblastoma |
125554311 | 12555431 | 2 | Nephroblastoma |
125554311 | 12555431 | 3 | Nephroblastoma |
125554311 | 12555431 | 4 | Nephroblastoma |
125554311 | 12555431 | 5 | Prophylaxis against diarrhoea |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125554311 | 12555431 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125554311 | 12555431 | Disease progression |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |