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
123165643 12316564 3 F 20160902 20160429 20160909 PER US-ALEXION-A201603034 ALEXION 0.00 M Y 0.00000 20160909 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
123165643 12316564 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) UNK U T3-AE4703B04 125166 CONCENTRATE FOR SOLUTION FOR INFUSION
123165643 12316564 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) UNK U T3-AE7318B01 125166 CONCENTRATE FOR SOLUTION FOR INFUSION
123165643 12316564 3 C CELLCEPT MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETIL HYDROCHLORIDE 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123165643 12316564 1 Haemolytic uraemic syndrome
123165643 12316564 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123165643 12316564 Blood creatinine increased
123165643 12316564 Decreased appetite
123165643 12316564 Neuralgia
123165643 12316564 Neuropathy peripheral
123165643 12316564 Weight decreased

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

no results found

Therapies reported

no results found