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
122813632 12281363 2 F 20160408 20160809 20160419 20160816 EXP CO-ALEXION PHARMACEUTICALS INC-A201602688 ALEXION 38.13 YR F Y 0.00000 20160816 CN CO CO

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
122813632 12281363 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 600 MG, QW AE1235B05 125166 600 MG CONCENTRATE FOR SOLUTION FOR INFUSION /wk
122813632 12281363 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, Q2W AE1235B05 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122813632 12281363 1 Paroxysmal nocturnal haemoglobinuria

Outcome of event

Event ID CASEID OUTC COD
122813632 12281363 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122813632 12281363 Arrhythmia
122813632 12281363 Autonomic nervous system imbalance
122813632 12281363 Bradycardia
122813632 12281363 Dizziness
122813632 12281363 Hypotension

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
122813632 12281363 1 20150529 20150619 0
122813632 12281363 2 20150626 0