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
122659764 12265976 4 F 20160707 20160413 20160715 EXP CA-PFIZER INC-2016204841 PFIZER 91.00 YR F Y 0.00000 20160715 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
122659764 12265976 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Oral 20 MG, WEEKLY Y 11719 20 MG /wk
122659764 12265976 2 SS SULFASALAZINE. SULFASALAZINE 1 Y 7073
122659764 12265976 3 SS ARAVA LEFLUNOMIDE 1 Oral 20 MG, 1X/DAY Y 0 20 MG QD
122659764 12265976 4 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Oral 400 MG, 1X/DAY 0 400 MG QD
122659764 12265976 5 SS PREDNISONE. PREDNISONE 1 Y 0
122659764 12265976 6 SS PREDNISONE. PREDNISONE 1 Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122659764 12265976 1 Rheumatoid arthritis
122659764 12265976 2 Rheumatoid arthritis
122659764 12265976 3 Rheumatoid arthritis
122659764 12265976 4 Rheumatoid arthritis
122659764 12265976 5 Rheumatoid arthritis
122659764 12265976 6 Pain

Outcome of event

Event ID CASEID OUTC COD
122659764 12265976 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122659764 12265976 Abasia
122659764 12265976 Disease progression
122659764 12265976 Drug ineffective
122659764 12265976 Drug intolerance
122659764 12265976 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
122659764 12265976 1 20151123 20160620 0
122659764 12265976 3 20150723 20151123 0
122659764 12265976 4 20150723 0