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
118869412 11886941 2 F 20150517 20160203 20160104 20160210 EXP GB-UCBSA-2015043599 UCB 30.30 YR F Y 0.00000 20160210 MD 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
118869412 11886941 1 PS Certolizumab pegol CERTOLIZUMAB PEGOL 1 Subcutaneous 200 MG, EV 2 WEEKS(QOW) 125160 200 MG QOW
118869412 11886941 2 C ETODOLAC. ETODOLAC 1 Oral 600 MG, ONCE DAILY (QD) U 0 600 MG QD
118869412 11886941 3 C TRAMADOL. TRAMADOL 1 Oral 50 MG U 0 50 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118869412 11886941 1 Rheumatoid arthritis
118869412 11886941 2 Rheumatoid arthritis
118869412 11886941 3 Rheumatoid arthritis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
118869412 11886941 Lower respiratory tract infection

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
118869412 11886941 1 20140618 0
118869412 11886941 2 20130405 0
118869412 11886941 3 20120503 0