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
123486066 12348606 6 F 201604 20160908 20160509 20160915 EXP CA-PFIZER INC-2016243328 PFIZER 69.00 YR F Y 0.00000 20160915 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
123486066 12348606 1 PS XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, 2X/DAY 203214 5 MG TABLET BID
123486066 12348606 2 SS XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, 2X/DAY 203214 5 MG TABLET BID
123486066 12348606 3 SS XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, 2X/DAY 203214 5 MG TABLET BID
123486066 12348606 4 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 25 MG, WEEKLY 11719 25 MG /wk
123486066 12348606 5 C CELEBREX CELECOXIB 1 200 MG, AS NEEDED 0 200 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123486066 12348606 1 Rheumatoid arthritis
123486066 12348606 4 Rheumatoid arthritis
123486066 12348606 5 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
123486066 12348606 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123486066 12348606 Alopecia
123486066 12348606 Cataract
123486066 12348606 Drug effect delayed

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
123486066 12348606 1 20160427 20160502 0
123486066 12348606 2 20160601 20160727 0
123486066 12348606 3 20160823 0