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
1125413614 11254136 14 F 2015 20160627 20150709 20160705 EXP CA-PFIZER INC-2015227267 PFIZER 66.00 YR F Y 0.00000 20160705 MD 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
1125413614 11254136 1 PS XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, 2X/DAY Y 203214 5 MG TABLET BID
1125413614 11254136 2 SS XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, 2X/DAY Y 203214 5 MG TABLET BID
1125413614 11254136 3 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Oral 20 MG, WEEKLY 11719 20 MG /wk
1125413614 11254136 4 SS PREDNISONE. PREDNISONE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
1125413614 11254136 1 Rheumatoid arthritis
1125413614 11254136 3 Rheumatoid arthritis
1125413614 11254136 4 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
1125413614 11254136 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
1125413614 11254136 Bronchitis
1125413614 11254136 Chronic obstructive pulmonary disease
1125413614 11254136 Condition aggravated
1125413614 11254136 Drug effect incomplete
1125413614 11254136 Fatigue
1125413614 11254136 Post procedural infection
1125413614 11254136 Respiratory tract infection
1125413614 11254136 Somnolence

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
1125413614 11254136 1 20150701 20150706 0
1125413614 11254136 2 20160210 201606 0