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
126455391 12645539 1 I 201603 20160801 20160811 20160811 EXP GB-MYLANLABS-2016M1032300 MYLAN 0.00 Y 0.00000 20160811 CN 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
126455391 12645539 1 PS TACROLIMUS. TACROLIMUS 1 Unknown UNK 90596
126455391 12645539 2 SS PREDNISONE. PREDNISONE 1 Unknown UNK 0
126455391 12645539 3 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 500 MG, Q2W 0 500 MG QOW
126455391 12645539 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
126455391 12645539 1 Product used for unknown indication
126455391 12645539 2 Product used for unknown indication
126455391 12645539 3 Haemolytic uraemic syndrome

Outcome of event

Event ID CASEID OUTC COD
126455391 12645539 HO
126455391 12645539 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126455391 12645539 Drug ineffective
126455391 12645539 Herpes zoster
126455391 12645539 Incorrect dose administered
126455391 12645539 Metapneumovirus infection
126455391 12645539 Osteonecrosis
126455391 12645539 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