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
126986022 12698602 2 F 201608 20160831 20160830 20160908 EXP US-ALEXION PHARMACEUTICALS INC-A201606298 ALEXION 53.36 YR M Y 0.00000 20160908 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
126986022 12698602 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) UNK 125166 CONCENTRATE FOR SOLUTION FOR INFUSION
126986022 12698602 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 1200 MG, Q2W 125166 1200 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126986022 12698602 1 Haemolytic uraemic syndrome

Outcome of event

Event ID CASEID OUTC COD
126986022 12698602 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126986022 12698602 Abdominal discomfort
126986022 12698602 Choking
126986022 12698602 Constipation
126986022 12698602 Decreased appetite
126986022 12698602 Dehydration
126986022 12698602 Dysphagia
126986022 12698602 Dysphonia
126986022 12698602 Fatigue
126986022 12698602 Headache
126986022 12698602 Malaise
126986022 12698602 Polyp
126986022 12698602 Urinary retention
126986022 12698602 Weight decreased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found