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
125592921 12559292 1 I 2016 20160711 20160715 20160715 EXP US-UCBSA-2016026129 UCB 0.00 F Y 0.00000 20160715 OT US US

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
125592921 12559292 1 PS CIMZIA CERTOLIZUMAB PEGOL 1 200 MG, EV 2 WEEKS(QOW) U U 902042 125160 200 MG POWDER AND SOLVENT FOR SOLUTION FOR INJECTION QOW
125592921 12559292 2 C PREDNISOLONE. PREDNISOLONE 1 UNK U 0
125592921 12559292 3 C ADVIL IBUPROFEN 1 UNK U 0
125592921 12559292 4 C ALEVE NAPROXEN SODIUM 1 UNK U 0
125592921 12559292 5 C ALPHAGAN P BRIMONIDINE TARTRATE 1 UNK U 0
125592921 12559292 6 C PREDNISOLONE ACETATE. PREDNISOLONE ACETATE 1 UNK U 0
125592921 12559292 7 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125592921 12559292 1 Rheumatoid arthritis
125592921 12559292 2 Product used for unknown indication
125592921 12559292 3 Product used for unknown indication
125592921 12559292 4 Product used for unknown indication
125592921 12559292 5 Product used for unknown indication
125592921 12559292 6 Product used for unknown indication
125592921 12559292 7 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125592921 12559292 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125592921 12559292 Rash

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
125592921 12559292 1 201604 0