The Safety Rates Drug Report

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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
125516301 12551630 1 I 20160628 20160713 20160713 EXP US-CIPLA LTD.-2016US09466 CIPLA REARDON DA, VREDENBURGH JJ, COAN A, DESJARDINS A, PETERS KB, GURURANGAN S, ET AL.,. PHASE I STUDY OF SUNITINIB AND IRINOTECAN FOR PATIENTS WITH RECURRENT MALIGNANT GLIOMA. J NEUROONCOL. 2011;105:621 TO 627 0.00 Y 0.00000 20160713 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
125516301 12551630 1 PS Irinotecan IRINOTECAN 1 Unknown UNK, PRIOR THERAPY U U 77219
125516301 12551630 2 SS Irinotecan IRINOTECAN 1 Intravenous (not otherwise specified) UNK, OVER 90 MIN ON DAYS 1, 15 AND 29 OF EACH 42 DAY CYCLE U U 77219
125516301 12551630 3 SS TEMOZOLOMIDE. TEMOZOLOMIDE 1 Unknown UNK, PRIOR THERAPY U U 0
125516301 12551630 4 SS Sunitinib SUNITINIB 1 Oral UNK, QD, WITHOUT REGARD TO FOOD ONCE A DAY FOR 4 WEEKS FOLLOWED BY A 2 WEEK REST U U 0
125516301 12551630 5 SS Bevacizumab BEVACIZUMAB 1 Unknown UNK, PRIOR THERAPY U U 0
125516301 12551630 6 SS VANDETANIB. VANDETANIB 1 Unknown UNK, PRIOR THERAPY U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125516301 12551630 1 Malignant glioma
125516301 12551630 3 Malignant glioma
125516301 12551630 4 Malignant glioma
125516301 12551630 5 Malignant glioma
125516301 12551630 6 Malignant glioma

Outcome of event

Event ID CASEID OUTC COD
125516301 12551630 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125516301 12551630 Disease progression
125516301 12551630 Hypertension

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found