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
122231102 12223110 2 F 201603 20160719 20160330 20160727 EXP US-ALEXION PHARMACEUTICALS INC-A201602088 ALEXION 0.00 F Y 0.00000 20160727 CN 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
122231102 12223110 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, Q2W 132870.656 MG Y T2-AE3115B03 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122231102 12223110 1 Paroxysmal nocturnal haemoglobinuria

Outcome of event

Event ID CASEID OUTC COD
122231102 12223110 OT
122231102 12223110 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122231102 12223110 Arthralgia
122231102 12223110 Electrocardiogram abnormal
122231102 12223110 Fatigue
122231102 12223110 Infusion site swelling
122231102 12223110 Initial insomnia
122231102 12223110 Lung disorder
122231102 12223110 Medication error
122231102 12223110 Pain in extremity
122231102 12223110 Pneumonia

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
122231102 12223110 1 20100610 20160706 0