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
125477221 12547722 1 I 20160513 20160705 20160712 20160712 EXP DE-UCBSA-2016025419 UCB 76.48 YR M Y 72.00000 KG 20160712 MD DE DE

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
125477221 12547722 1 PS CIMZIA CERTOLIZUMAB PEGOL 1 Subcutaneous 200 MG, EV 2 WEEKS(QOW) Y U 125160 200 MG SOLUTION FOR INJECTION QOW
125477221 12547722 2 C MTX METHOTREXATE SODIUM 1 Oral 10 MG, WEEKLY (QW) 0 10 MG /wk
125477221 12547722 3 C Prednisolon PREDNISOLONE 1 Oral 5 MG, ONCE DAILY (QD) 0 5 MG QD
125477221 12547722 4 C IBUPROFEN. IBUPROFEN 1 Oral 600 MG, UNK 0 600 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125477221 12547722 1 Rheumatoid arthritis
125477221 12547722 2 Rheumatoid arthritis
125477221 12547722 3 Rheumatoid arthritis
125477221 12547722 4 Pain

Outcome of event

Event ID CASEID OUTC COD
125477221 12547722 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125477221 12547722 Pneumonia

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
125477221 12547722 1 20140603 20160513 0
125477221 12547722 2 20070727 0
125477221 12547722 3 20150216 0
125477221 12547722 4 20080603 0