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
127614861 12761486 1 I 20160908 20160920 20160920 EXP FR-ALEXION PHARMACEUTICALS INC-A201606864 ALEXION 25.00 YR F Y 0.00000 20160920 OT FR FR

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
127614861 12761486 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) UNK 125166 CONCENTRATE FOR SOLUTION FOR INFUSION
127614861 12761486 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, QW 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION /wk
127614861 12761486 3 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
127614861 12761486 1 Haemolytic uraemic syndrome

Outcome of event

Event ID CASEID OUTC COD
127614861 12761486 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127614861 12761486 Abortion induced
127614861 12761486 Acute kidney injury
127614861 12761486 Exposure during pregnancy
127614861 12761486 Haemolytic uraemic syndrome
127614861 12761486 Renal impairment

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
127614861 12761486 1 201202 0