The Safety Rates Drug Report

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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
126620871 12662087 1 I 201511 20160803 20160817 20160817 EXP E2B_00584714 CA-HQ SPECIALTY-CA-2016INT000786 INTERCHEM 65.00 YR F Y 0.00000 20160817 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
126620871 12662087 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Unknown UNK 201749
126620871 12662087 2 SS ENBREL ETANERCEPT 1 UNK Y 0
126620871 12662087 3 SS SULFASALAZINE. SULFASALAZINE 1 Unknown UNK Y 0
126620871 12662087 4 SS ARTHROTEC DICLOFENAC SODIUMMISOPROSTOL 1 Unknown UNK U 0
126620871 12662087 5 SS CELEBREX CELECOXIB 1 Unknown UNK 0
126620871 12662087 6 SS ARAVA LEFLUNOMIDE 1 Unknown UNK U 0
126620871 12662087 7 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126620871 12662087 1 Rheumatoid arthritis
126620871 12662087 2 Rheumatoid arthritis
126620871 12662087 3 Rheumatoid arthritis
126620871 12662087 4 Rheumatoid arthritis
126620871 12662087 5 Rheumatoid arthritis
126620871 12662087 6 Rheumatoid arthritis
126620871 12662087 7 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
126620871 12662087 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126620871 12662087 Joint arthroplasty
126620871 12662087 Joint destruction
126620871 12662087 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
126620871 12662087 2 2013 201511 0