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
118009954 11800995 4 F 20151012 20160728 20151204 20160809 EXP US-ALEXION-A201504786 ALEXION 0.00 F Y 0.00000 20160809 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
118009954 11800995 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) UNK T2-AD4280B01 125166 CONCENTRATE FOR SOLUTION FOR INFUSION
118009954 11800995 2 SS GEMZAR GEMCITABINE HYDROCHLORIDE 1 Unknown UNK Y 0
118009954 11800995 3 SS GEMZAR GEMCITABINE HYDROCHLORIDE 1 Unknown UNK Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118009954 11800995 1 Haemolytic uraemic syndrome
118009954 11800995 2 Pancreatic carcinoma

Outcome of event

Event ID CASEID OUTC COD
118009954 11800995 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
118009954 11800995 Abdominal pain
118009954 11800995 Fatigue
118009954 11800995 Iron deficiency anaemia

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
118009954 11800995 3 20151026 0