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
102693374 10269337 4 F 2013 20160923 20140701 20160930 EXP CA-UCBSA-2014003763 UCB 0.00 F Y 58.96000 KG 20160930 CN 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
102693374 10269337 1 PS Certolizumab pegol RA CERTOLIZUMAB PEGOL 1 Subcutaneous 400 MG, EV 2 WEEKS(QOW) Y U 125160 400 MG QOW
102693374 10269337 2 SS Certolizumab pegol RA CERTOLIZUMAB PEGOL 1 Subcutaneous 200 MG, EV 2 WEEKS(QOW) Y U 125160 200 MG QOW
102693374 10269337 3 C METHOTREXATE. METHOTREXATE 1 Oral 15 MG, WEEKLY (QW) U 0 15 MG /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
102693374 10269337 1 Rheumatoid arthritis
102693374 10269337 3 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
102693374 10269337 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
102693374 10269337 Psoriasis

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
102693374 10269337 1 20130117 20130214 0
102693374 10269337 2 201301 201406 0
102693374 10269337 3 2010 0