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
126665311 12666531 1 I 20111122 20130325 20160819 20160819 EXP BE-ROCHE-1815906 ROCHE 74.44 YR M Y 0.00000 20160819 MD BE BE

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
126665311 12666531 1 PS Bevacizumab BEVACIZUMAB 1 Unknown U 125085
126665311 12666531 2 SS 5-FU FLUOROURACIL 1 Unknown U 0
126665311 12666531 3 SS IRINOTECAN IRINOTECAN 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126665311 12666531 1 Colorectal cancer metastatic
126665311 12666531 2 Colorectal cancer metastatic
126665311 12666531 3 Colorectal cancer metastatic

Outcome of event

Event ID CASEID OUTC COD
126665311 12666531 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126665311 12666531 Anaemia
126665311 12666531 Hemiplegia
126665311 12666531 Hypertension
126665311 12666531 Proteinuria
126665311 12666531 Rash erythematous
126665311 12666531 Speech disorder
126665311 12666531 Transient ischaemic attack

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

no results found

Therapies reported

no results found