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
126295683 12629568 3 F 20160718 20160831 20160808 20160907 EXP BR-ALEXION-A201605620 ALEXION 26.90 YR F Y 0.00000 20160907 CN BR BR

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
126295683 12629568 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 600 MG, UNK Y 125166 600 MG CONCENTRATE FOR SOLUTION FOR INFUSION
126295683 12629568 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, UNK Y 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION
126295683 12629568 3 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, QW Y 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126295683 12629568 1 Paroxysmal nocturnal haemoglobinuria

Outcome of event

Event ID CASEID OUTC COD
126295683 12629568 OT
126295683 12629568 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126295683 12629568 Back pain
126295683 12629568 Blood pressure increased
126295683 12629568 Chromaturia
126295683 12629568 Dyspnoea
126295683 12629568 Haemolysis
126295683 12629568 Inappropriate schedule of drug administration
126295683 12629568 Loss of consciousness
126295683 12629568 Seizure
126295683 12629568 Syncope

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
126295683 12629568 1 20140924 0
126295683 12629568 3 20160718 20160801 0