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
103571317 10357131 7 F 201404 20160913 20140801 20160920 EXP AU-ALEXION PHARMACEUTICALS INC.-A201402927 ALEXION 81.61 YR F Y 0.00000 20160920 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
103571317 10357131 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 600 MG, QW 125166 600 MG CONCENTRATE FOR SOLUTION FOR INFUSION /wk
103571317 10357131 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
103571317 10357131 1 Paroxysmal nocturnal haemoglobinuria

Outcome of event

Event ID CASEID OUTC COD
103571317 10357131 HO
103571317 10357131 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
103571317 10357131 Arthralgia
103571317 10357131 Blood lactate dehydrogenase increased
103571317 10357131 Carpal tunnel syndrome
103571317 10357131 Cholecystitis
103571317 10357131 Cholelithiasis
103571317 10357131 Circulatory collapse
103571317 10357131 Musculoskeletal pain
103571317 10357131 Pain
103571317 10357131 Pain in extremity
103571317 10357131 Syncope
103571317 10357131 Urinary tract infection

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
103571317 10357131 1 201111 0