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
115954754 11595475 4 F 20160922 20151006 20160929 EXP CA-UCBSA-2015031200 UCB 0.00 F Y 0.00000 20160929 MD CA CA

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
115954754 11595475 1 PS Certolizumab pegol RA CERTOLIZUMAB PEGOL 1 Subcutaneous 400 MG, EV 2 WEEKS(QOW) 121121 125160 400 MG SOLUTION FOR INJECTION QOW
115954754 11595475 2 SS Certolizumab pegol RA CERTOLIZUMAB PEGOL 1 Subcutaneous 200 MG, EV 2 WEEKS(QOW) 125160 200 MG SOLUTION FOR INJECTION QOW
115954754 11595475 3 SS Certolizumab pegol RA CERTOLIZUMAB PEGOL 1 Subcutaneous 200 MG, EV 2 WEEKS(QOW) 125160 200 MG SOLUTION FOR INJECTION QOW
115954754 11595475 4 SS Thalidomide THALIDOMIDE 1 UNK U U 0
115954754 11595475 5 C PREDNISONE. PREDNISONE 1 UNK U U 0
115954754 11595475 6 C PREDNISONE. PREDNISONE 1 UNK U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115954754 11595475 1 Rheumatoid arthritis
115954754 11595475 4 Eczema
115954754 11595475 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
115954754 11595475 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
115954754 11595475 Eczema
115954754 11595475 Infection
115954754 11595475 Localised infection
115954754 11595475 Pleural effusion

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
115954754 11595475 1 20140926 20141012 0
115954754 11595475 2 20141026 0
115954754 11595475 3 20151030 0