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
111270845 11127084 5 F 20150102 20160715 20150521 20160726 EXP US-ALEXION PHARMACEUTICALS INC.-A201501727 ALEXION 26.89 YR M Y 0.00000 20160726 CN 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
111270845 11127084 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 1200 MG, Q2W N T2-AC1965B01 125166 1200 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
111270845 11127084 1 Haemolytic uraemic syndrome

Outcome of event

Event ID CASEID OUTC COD
111270845 11127084 HO
111270845 11127084 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
111270845 11127084 Blood creatinine increased
111270845 11127084 Cerebral thrombosis
111270845 11127084 Condition aggravated
111270845 11127084 Cyanosis
111270845 11127084 Dehydration
111270845 11127084 Memory impairment
111270845 11127084 Pneumonia
111270845 11127084 Seizure
111270845 11127084 Sepsis

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
111270845 11127084 1 20130622 20160714 0