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
126027902 12602790 2 F 201606 20160801 20160728 20160810 EXP CA-PFIZER INC-2016354390 PFIZER 78.00 YR F Y 0.00000 20160810 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
126027902 12602790 1 PS XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, 2X/DAY 203214 5 MG TABLET BID
126027902 12602790 2 SS CELEBREX CELECOXIB 1 Oral UNK 20998 CAPSULE, HARD
126027902 12602790 3 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Oral UNK Y 11719 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126027902 12602790 1 Rheumatoid arthritis
126027902 12602790 2 Rheumatoid arthritis
126027902 12602790 3 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
126027902 12602790 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126027902 12602790 Back pain
126027902 12602790 Constipation
126027902 12602790 Cystitis
126027902 12602790 Haematochezia
126027902 12602790 Haemorrhoids
126027902 12602790 Rectal haemorrhage

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
126027902 12602790 1 20150509 0
126027902 12602790 3 20160621 0