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
126451352 12645135 2 F 201504 20160914 20160811 20160921 EXP AU-ALEXION-A201501919 ALEXION 52.67 YR M Y 0.00000 20160921 CN AU AU

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
126451352 12645135 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 600 MG, QW 125166 600 MG CONCENTRATE FOR SOLUTION FOR INFUSION /wk
126451352 12645135 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, Q2W 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126451352 12645135 1 Paroxysmal nocturnal haemoglobinuria

Outcome of event

Event ID CASEID OUTC COD
126451352 12645135 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126451352 12645135 Bilirubin conjugated increased
126451352 12645135 Blood bilirubin increased
126451352 12645135 Blood lactate dehydrogenase increased
126451352 12645135 Chromaturia
126451352 12645135 Cough
126451352 12645135 Extravascular haemolysis
126451352 12645135 Haemoglobin decreased
126451352 12645135 Nasopharyngitis

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
126451352 12645135 1 20130422 20130513 0
126451352 12645135 2 20130520 0