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
126784571 12678457 1 I 20141205 20141219 20160823 20160823 EXP BR-ALEXION PHARMACEUTICALS INC.-A201405045 ALEXION 6.00 YR F Y 0.00000 20160823 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
126784571 12678457 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
126784571 12678457 1 Haemolytic uraemic syndrome

Outcome of event

Event ID CASEID OUTC COD
126784571 12678457 DE
126784571 12678457 HO
126784571 12678457 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126784571 12678457 Anuria
126784571 12678457 Blood lactate dehydrogenase abnormal
126784571 12678457 Cardiac arrest
126784571 12678457 Cardio-respiratory arrest
126784571 12678457 Cerebral ischaemia
126784571 12678457 Depression
126784571 12678457 Hypertension
126784571 12678457 Necrosis
126784571 12678457 Oedema
126784571 12678457 Pain
126784571 12678457 Polyuria
126784571 12678457 Seizure

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
126784571 12678457 1 20141128 20141216 0