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
116903089 11690308 9 F 20160704 20151102 20160712 EXP CA-PFIZER INC-2015329399 PFIZER 62.00 YR F Y 0.00000 20160712 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
116903089 11690308 1 PS XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, 2X/DAY Y 203214 5 MG TABLET BID
116903089 11690308 2 SS XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, 2X/DAY Y 203214 5 MG TABLET BID
116903089 11690308 3 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Subcutaneous 25 MG, WEEKLY Y 11719 25 MG SOLUTION FOR INJECTION /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116903089 11690308 1 Rheumatoid arthritis
116903089 11690308 3 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
116903089 11690308 OT
116903089 11690308 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
116903089 11690308 Arthropathy
116903089 11690308 Pain
116903089 11690308 Pneumonia
116903089 11690308 Pulmonary mass

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
116903089 11690308 1 20141006 201509 0
116903089 11690308 2 20151214 20160203 0
116903089 11690308 3 20160203 0