The Safety Rates Drug Report

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Drug     Injury     Quarter    

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
126963091 12696309 1 I 20160824 20160830 20160830 EXP CA-ROCHE-1819631 ROCHE 45.00 YR F Y 96.00000 KG 20160830 OT CA CA

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
126963091 12696309 1 PS AVASTIN BEVACIZUMAB 1 Intravenous (not otherwise specified) FREQUENCY: CYCLICAL U 125085 960 MG SOLUTION FOR INFUSION
126963091 12696309 2 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral U 0 2 MG
126963091 12696309 3 SS DILANTIN PHENYTOIN 1 Intravenous (not otherwise specified) U 0
126963091 12696309 4 C DIAMICRON GLICLAZIDE 1 Unknown 0 TABLET
126963091 12696309 5 C PANTOPRAZOLE SODIUM. PANTOPRAZOLE SODIUM 1 0
126963091 12696309 6 C SITAGLIPTIN PHOSPHATE SITAGLIPTIN PHOSPHATE 1 0
126963091 12696309 7 C VITAMIN B12 CYANOCOBALAMIN 1 Unknown AS REQUIRED 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126963091 12696309 1 Glioblastoma
126963091 12696309 2 Glioblastoma
126963091 12696309 3 Seizure

Outcome of event

Event ID CASEID OUTC COD
126963091 12696309 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126963091 12696309 Amnesia
126963091 12696309 Confusional state
126963091 12696309 Diarrhoea
126963091 12696309 Hypersensitivity
126963091 12696309 Hypertension
126963091 12696309 Malignant neoplasm progression
126963091 12696309 Seizure
126963091 12696309 Skin disorder
126963091 12696309 Skin striae
126963091 12696309 Skin ulcer
126963091 12696309 White blood cell count decreased

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

no results found

Therapies reported

no results found