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
111294334 11129433 4 F 20150511 20160823 20150521 20160830 EXP US-ALEXION-A201501752 ALEXION 0.00 F Y 0.00000 20160830 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
111294334 11129433 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) UNK U T2-AD4285B01 125166 CONCENTRATE FOR SOLUTION FOR INFUSION
111294334 11129433 2 SS HYDRALAZINE HYDRALAZINE HYDROCHLORIDE 1 Unknown UNK Y 0
111294334 11129433 3 SS CELLCEPT MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETIL HYDROCHLORIDE 1 Unknown UNK Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
111294334 11129433 1 Haemolytic uraemic syndrome
111294334 11129433 2 Product used for unknown indication
111294334 11129433 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
111294334 11129433 HO
111294334 11129433 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
111294334 11129433 Anaemia
111294334 11129433 Bone marrow failure
111294334 11129433 Condition aggravated
111294334 11129433 Diarrhoea
111294334 11129433 Drug ineffective
111294334 11129433 Fatigue
111294334 11129433 Haemoglobin decreased
111294334 11129433 Haemolytic uraemic syndrome
111294334 11129433 Haemorrhage
111294334 11129433 Motor dysfunction

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

no results found

Therapies reported

no results found