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
126583562 12658356 2 F 20160822 20160817 20160830 EXP US-ALEXION PHARMACEUTICALS INC-A201605899 ALEXION 0.00 M Y 0.00000 20160830 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
126583562 12658356 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 1200 MG, UNK Y 125166 1200 MG CONCENTRATE FOR SOLUTION FOR INFUSION
126583562 12658356 2 C RITUXIMAB RITUXIMAB 1 Intravenous (not otherwise specified) UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126583562 12658356 1 Haemolytic uraemic syndrome
126583562 12658356 2 Glomerulonephritis membranoproliferative

Outcome of event

Event ID CASEID OUTC COD
126583562 12658356 HO
126583562 12658356 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126583562 12658356 Dyspnoea
126583562 12658356 Hypertensive crisis
126583562 12658356 Kidney fibrosis
126583562 12658356 Oedema
126583562 12658356 Renal impairment
126583562 12658356 Swelling

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
126583562 12658356 1 20160306 20160616 0
126583562 12658356 2 20160707 20160721 0