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
108466034 10846603 4 F 20150217 20160922 20150220 20160929 EXP US-ALEXION-A201500597 ALEXION 0.00 F Y 0.00000 20160929 MD 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
108466034 10846603 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) UNK T2-AD3636B01 125166 CONCENTRATE FOR SOLUTION FOR INFUSION
108466034 10846603 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
108466034 10846603 1 Paroxysmal nocturnal haemoglobinuria

Outcome of event

Event ID CASEID OUTC COD
108466034 10846603 HO
108466034 10846603 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
108466034 10846603 Anal incontinence
108466034 10846603 Arthralgia
108466034 10846603 Back pain
108466034 10846603 Deep vein thrombosis
108466034 10846603 Intervertebral disc protrusion
108466034 10846603 Pain in extremity

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

no results found

Therapies reported

no results found