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
123260004 12326000 4 F 201603 20160720 20160503 20160728 EXP GB-ALEXION PHARMACEUTICALS INC-A201603086 ALEXION 59.19 YR F Y 0.00000 20160728 CN GB GB

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
123260004 12326000 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 500 MG, Q2W 125166 500 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
123260004 12326000 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 1200 MG, Q2W 125166 1200 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
123260004 12326000 3 SS PREDNISONE. PREDNISONE 1 Unknown UNK 0
123260004 12326000 4 SS TACROLIMUS. TACROLIMUS 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123260004 12326000 1 Haemolytic uraemic syndrome
123260004 12326000 3 Product used for unknown indication
123260004 12326000 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123260004 12326000 HO
123260004 12326000 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123260004 12326000 Drug ineffective
123260004 12326000 Herpes zoster
123260004 12326000 Incorrect dose administered
123260004 12326000 Metapneumovirus infection
123260004 12326000 Osteonecrosis
123260004 12326000 Respiratory tract infection

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

no results found

Therapies reported

no results found