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
126793771 12679377 1 I 20150725 20150729 20160824 20160824 EXP BR-ALEXION PHARMACEUTICALS INC-A201505595 ALEXION 36.00 YR F Y 60.00000 KG 20160824 CN BR BR

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
126793771 12679377 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, QW 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION /wk
126793771 12679377 2 C ROCEPHIN CEFTRIAXONE SODIUM 1 Intravenous (not otherwise specified) 500 MG, UNK 0 500 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126793771 12679377 1 Haemolytic uraemic syndrome
126793771 12679377 2 Meningococcal infection

Outcome of event

Event ID CASEID OUTC COD
126793771 12679377 OT
126793771 12679377 HO
126793771 12679377 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126793771 12679377 Blood lactate dehydrogenase increased
126793771 12679377 Cardio-respiratory arrest
126793771 12679377 Confusional state
126793771 12679377 Diarrhoea
126793771 12679377 Exposure during pregnancy
126793771 12679377 Renal impairment
126793771 12679377 Thrombocytopenia
126793771 12679377 Vomiting

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
126793771 12679377 1 20110722 0
126793771 12679377 2 20150722 0