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
113809862 11380986 2 F 20140821 20160629 20150814 20160707 EXP CA-AMGEN-CANSP2014105527 AMGEN 27.00 YR A F Y 0.00000 20160707 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
113809862 11380986 1 PS ENBREL ETANERCEPT 1 Unknown UNK U 103795 UNKNOWN FORMULATION
113809862 11380986 2 SS METHOTREXATE. METHOTREXATE 1 Oral 20 MG, QWK 0 20 MG /wk
113809862 11380986 3 SS CIMZIA CERTOLIZUMAB PEGOL 1 Unknown UNK 0
113809862 11380986 4 SS PREDNISONE. PREDNISONE 1 Unknown UNK 0
113809862 11380986 5 SS XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, BID 0 5 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113809862 11380986 1 Rheumatoid arthritis
113809862 11380986 2 Rheumatoid arthritis
113809862 11380986 3 Product used for unknown indication
113809862 11380986 4 Product used for unknown indication
113809862 11380986 5 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
113809862 11380986 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
113809862 11380986 Activities of daily living impaired
113809862 11380986 Emotional disorder
113809862 11380986 Joint swelling
113809862 11380986 Motor dysfunction
113809862 11380986 Rheumatoid arthritis

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
113809862 11380986 2 20121018 20130425 0
113809862 11380986 5 20140917 0