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
126767792 12676779 2 F 201204 20160823 20160823 20160829 EXP BR-ALEXION PHARMACEUTICALS INC-A201606110 ALEXION 0.00 F Y 0.00000 20160829 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
126767792 12676779 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) UNK 125166 CONCENTRATE FOR SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126767792 12676779 1 Paroxysmal nocturnal haemoglobinuria

Outcome of event

Event ID CASEID OUTC COD
126767792 12676779 HO
126767792 12676779 OT
126767792 12676779 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126767792 12676779 Cellulitis
126767792 12676779 Facial pain
126767792 12676779 Gastric haemorrhage
126767792 12676779 Haemoglobinuria
126767792 12676779 Haemolysis
126767792 12676779 Headache
126767792 12676779 Hyperglycaemia
126767792 12676779 Infection

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
126767792 12676779 1 20111205 0