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
122052462 12205246 2 F 20160309 20160701 20160323 20160712 EXP FR-ALEXION PHARMACEUTICALS INC-A201601905 ALEXION 32.90 YR F Y 53.00000 KG 20160712 CN FR FR

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
122052462 12205246 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 1200 MG, EVERY 21 DAYS U P00003905 125166 1200 MG CONCENTRATE FOR SOLUTION FOR INFUSION
122052462 12205246 2 SS TACROLIMUS. TACROLIMUS 1 Unknown UNK U 0
122052462 12205246 3 SS MMF MYCOPHENOLATE MOFETIL 1 Endocervical UNK U 0
122052462 12205246 4 C SODIUM CHLORIDE. SODIUM CHLORIDE 1 Unknown 9 %, UNK 0 9 PCT

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122052462 12205246 1 Product used for unknown indication
122052462 12205246 2 Immunosuppression
122052462 12205246 3 Immunosuppression
122052462 12205246 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
122052462 12205246 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122052462 12205246 Gastrointestinal disorder
122052462 12205246 Influenza
122052462 12205246 Nausea
122052462 12205246 Pyrexia
122052462 12205246 Rotavirus infection
122052462 12205246 Vomiting

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

no results found

Therapies reported

no results found