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
99179335 9917933 5 F 20131106 20160728 20140222 20160802 EXP GB-ROCHE-1351179 ROCHE 66.52 YR F Y 66.20000 KG 20160802 MD GB GB

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
99179335 9917933 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) LAST DOSE PRIOR TO SAE: 20/NOV/2013 125085 325 MG
99179335 9917933 2 C DALTEPARIN DALTEPARIN 1 Unknown 12500 UNITS 0
99179335 9917933 3 C DEXAMETHASONE. DEXAMETHASONE 1 Oral 0 4 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
99179335 9917933 1 Colon cancer
99179335 9917933 2 Thrombosis

Outcome of event

Event ID CASEID OUTC COD
99179335 9917933 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
99179335 9917933 Dysaesthesia
99179335 9917933 Epistaxis
99179335 9917933 Fatigue
99179335 9917933 Nausea
99179335 9917933 Palmar-plantar erythrodysaesthesia syndrome
99179335 9917933 Superior vena cava occlusion

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
99179335 9917933 1 20131106 20140709 0
99179335 9917933 2 20140210 0
99179335 9917933 3 20140212 20140219 0