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
118439726 11843972 6 F 2015 20160727 20151217 20160803 PER US-ALEXION-A201505076 ALEXION 37.10 YR F Y 0.00000 20160803 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
118439726 11843972 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) UNK Y T3-AE1224B01 125166 CONCENTRATE FOR SOLUTION FOR INFUSION
118439726 11843972 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 1200 MG, Q2W Y 125166 1200 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
118439726 11843972 3 C LABETALOL LABETALOLLABETALOL HYDROCHLORIDE 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118439726 11843972 1 Haemolytic uraemic syndrome
118439726 11843972 3 Hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
118439726 11843972 Blood pressure fluctuation
118439726 11843972 Exposure during pregnancy
118439726 11843972 Fatigue
118439726 11843972 Nausea
118439726 11843972 Protein urine
118439726 11843972 Swelling

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
118439726 11843972 1 20150911 0
118439726 11843972 2 20151009 20151218 0