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
120780934 12078093 4 F 201411 20160715 20160215 20160725 EXP CA-PFIZER INC-2014304761 PFIZER 52.00 YR F Y 0.00000 20160725 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
120780934 12078093 1 PS XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, 2X/DAY Y 203214 5 MG TABLET BID
120780934 12078093 2 SS XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, 2X/DAY Y 203214 5 MG TABLET BID
120780934 12078093 3 SS PREDNISONE. PREDNISONE 1 Oral 15 MG, DAILY 0 15 MG
120780934 12078093 4 C TYLENOL ACETAMINOPHEN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120780934 12078093 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
120780934 12078093 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
120780934 12078093 Bone pain
120780934 12078093 Condition aggravated
120780934 12078093 Diarrhoea
120780934 12078093 Disease recurrence
120780934 12078093 Headache
120780934 12078093 Oral candidiasis
120780934 12078093 Pain
120780934 12078093 Rheumatoid arthritis
120780934 12078093 Tooth disorder
120780934 12078093 Upper respiratory tract infection
120780934 12078093 Vulval cancer
120780934 12078093 Vulvovaginal burning sensation
120780934 12078093 Vulvovaginal disorder
120780934 12078093 Vulvovaginal dryness
120780934 12078093 Vulvovaginal pain
120780934 12078093 Vulvovaginal swelling

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
120780934 12078093 1 20141010 20141103 0