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
127419881 12741988 1 I 20160707 20160907 20160914 20160914 PER US-ALEXION PHARMACEUTICALS INC.-A201606713 ALEXION 8.09 YR F Y 0.00000 20160914 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
127419881 12741988 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, Q2W 24300 MG N 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
127419881 12741988 2 C PREDNISONE. PREDNISONE 1 Unknown 0
127419881 12741988 3 C LABETALOL LABETALOLLABETALOL HYDROCHLORIDE 1 Unknown 0
127419881 12741988 4 C AMLODIPINE AMLODIPINE BESYLATE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127419881 12741988 1 Haemolytic uraemic syndrome
127419881 12741988 2 Autoimmune disorder
127419881 12741988 3 Hypertension
127419881 12741988 4 Hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127419881 12741988 Drug ineffective
127419881 12741988 Nasopharyngitis

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
127419881 12741988 1 20150629 20160706 0