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
126387381 12638738 1 I 201603 20160801 20160809 20160809 EXP PHHY2016GB105663 SANDOZ 60.00 YR F Y 0.00000 20160809 OT GB GB

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
126387381 12638738 1 PS TACROLIMUS. TACROLIMUS 1 Unknown UNK 65461
126387381 12638738 2 SS PREDNISONE. PREDNISONE 1 Unknown UNK 0
126387381 12638738 3 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 500 MG, Q2W 0 500 MG
126387381 12638738 4 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 1200 MG, Q2W 0 1200 MG QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126387381 12638738 1 Product used for unknown indication
126387381 12638738 2 Product used for unknown indication
126387381 12638738 3 Haemolytic uraemic syndrome

Outcome of event

Event ID CASEID OUTC COD
126387381 12638738 OT
126387381 12638738 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126387381 12638738 Drug ineffective
126387381 12638738 Herpes zoster
126387381 12638738 Incorrect dose administered
126387381 12638738 Metapneumovirus infection
126387381 12638738 Osteonecrosis
126387381 12638738 Respiratory tract infection

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

no results found

Therapies reported

no results found