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
126571671 12657167 1 I 20160720 20160721 20160816 20160816 EXP BR-ALEXION PHARMACEUTICALS INC-A201605533 ALEXION 20.02 YR M Y 0.00000 20160816 CN BR BR

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
126571671 12657167 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, UNK 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION
126571671 12657167 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 1200 MG, UNK 125166 1200 MG CONCENTRATE FOR SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126571671 12657167 1 Haemolytic uraemic syndrome

Outcome of event

Event ID CASEID OUTC COD
126571671 12657167 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126571671 12657167 Abasia
126571671 12657167 Arrhythmia
126571671 12657167 Confusional state
126571671 12657167 Feeling abnormal
126571671 12657167 Headache
126571671 12657167 Influenza
126571671 12657167 Memory impairment
126571671 12657167 Pain
126571671 12657167 Pain in extremity
126571671 12657167 Urinary tract infection
126571671 12657167 Vomiting

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
126571671 12657167 1 20141113 20141204 0
126571671 12657167 2 20141214 0