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
114315634 11431563 4 F 20150921 20160805 20150828 20160816 EXP US-ALEXION PHARMACEUTICALS INC-A201503231 ALEXION 80.00 YR F Y 0.00000 20160816 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
114315634 11431563 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, UNK T3-AD5336B01 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION
114315634 11431563 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, UNK AD7698B02 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114315634 11431563 1 Haemolytic uraemic syndrome

Outcome of event

Event ID CASEID OUTC COD
114315634 11431563 HO
114315634 11431563 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
114315634 11431563 Drug ineffective
114315634 11431563 Vomiting

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
114315634 11431563 1 20150807 0
114315634 11431563 2 201509 0