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
121811355 12181135 5 F 20160729 20160315 20160808 EXP CA-PFIZER INC-2016150655 PFIZER 52.00 YR M Y 0.00000 20160808 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
121811355 12181135 1 PS XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, 2X/DAY 203214 5 MG TABLET BID
121811355 12181135 2 SS CELEBREX CELECOXIB 1 Oral 200 MG, AS NEEDED 20998 200 MG CAPSULE, HARD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121811355 12181135 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
121811355 12181135 OT
121811355 12181135 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
121811355 12181135 Headache
121811355 12181135 Joint effusion
121811355 12181135 Ligament sprain
121811355 12181135 Mobility decreased
121811355 12181135 Musculoskeletal stiffness
121811355 12181135 Pain
121811355 12181135 Sensitivity to weather change
121811355 12181135 Swelling
121811355 12181135 Synovial fluid white blood cells positive

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
121811355 12181135 1 20160229 0