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
124333394 12433339 4 F 20160524 20160722 20160603 20160801 EXP US-ALEXION PHARMACEUTICALS INC-A201603988 ALEXION 65.28 YR M Y 0.00000 20160801 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
124333394 12433339 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, QW U 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124333394 12433339 1 Paroxysmal nocturnal haemoglobinuria

Outcome of event

Event ID CASEID OUTC COD
124333394 12433339 HO
124333394 12433339 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124333394 12433339 Abdominal pain
124333394 12433339 Arthralgia
124333394 12433339 Epiglottitis
124333394 12433339 Febrile neutropenia
124333394 12433339 Haemoglobin decreased
124333394 12433339 Joint swelling
124333394 12433339 Pharyngitis
124333394 12433339 Platelet count decreased
124333394 12433339 Renal infarct
124333394 12433339 Splenic infarction
124333394 12433339 White blood cell count decreased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found