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
124775522 12477552 2 F 20160723 20160617 20160805 EXP CA-HQ SPECIALTY-CA-2016INT000382 INTERCHEM 51.00 YR F Y 0.00000 20160805 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
124775522 12477552 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Oral 20 MG, ON THURSDAYS 201749 20 MG TABLET
124775522 12477552 2 SS XELJANZ TOFACITINIB CITRATE 1 Oral 10 MG (5 MG, 2 IN 1 D) N 0 5 MG
124775522 12477552 3 SS CELEBREX CELECOXIB 1 Oral 1 D 0
124775522 12477552 4 SS FOLIC ACID. FOLIC ACID 1 Oral EXCEPT THURSDAY (5 MG, 1 D) 0 5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124775522 12477552 1 Rheumatoid arthritis
124775522 12477552 2 Rheumatoid arthritis
124775522 12477552 3 Rheumatoid arthritis
124775522 12477552 4 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
124775522 12477552 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124775522 12477552 Activities of daily living impaired
124775522 12477552 Myalgia
124775522 12477552 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
124775522 12477552 2 20151128 20160531 0