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
119852252 11985225 2 F 20160629 20160201 20160708 EXP CA-CONCORDIA PHARMACEUTICALS INC.-CO-PL-CA-2016-026 CONCORDIA 0.00 F Y 0.00000 20160708 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
119852252 11985225 1 PS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 9768 400 MG QD
119852252 11985225 2 SS LEFLUNOMIDE. LEFLUNOMIDE 1 0 20 MG QD
119852252 11985225 3 SS CELEBREX CELECOXIB 1 9768
119852252 11985225 4 SS TORADOL KETOROLAC TROMETHAMINE 1 9768
119852252 11985225 5 C METHOTREXATE. METHOTREXATE 1 0
119852252 11985225 6 C SULFASALAZINE. SULFASALAZINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119852252 11985225 1 Rheumatoid arthritis
119852252 11985225 2 Product used for unknown indication
119852252 11985225 3 Rheumatoid arthritis
119852252 11985225 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
119852252 11985225 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119852252 11985225 Fatigue
119852252 11985225 Infection
119852252 11985225 Pain
119852252 11985225 Rheumatoid arthritis
119852252 11985225 Therapy non-responder

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
119852252 11985225 1 20150817 0
119852252 11985225 2 20141201 20150505 0
119852252 11985225 3 20160520 0
119852252 11985225 5 20140709 20150501 0
119852252 11985225 6 20150817 20150830 0