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
125894581 12589458 1 I 2016 20160713 20160725 20160725 EXP CA-PFIZER INC-2016348248 PFIZER 0.00 A F Y 0.00000 20160725 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
125894581 12589458 1 PS XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, 1X/DAY 203214 5 MG TABLET QD
125894581 12589458 2 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Subcutaneous 25 MG, WEEKLY 11719 25 MG SOLUTION FOR INJECTION /wk
125894581 12589458 3 SS SULFASALAZINE. SULFASALAZINE 1 Oral 500 MG, 2X/DAY N 7073 500 MG BID
125894581 12589458 4 SS LEFLUNOMIDE. LEFLUNOMIDE 1 20 MG, DAILY N 0 20 MG
125894581 12589458 5 C CELEBREX CELECOXIB 1 Oral 200 MG, DAILY 0 200 MG
125894581 12589458 6 C FOLIC ACID. FOLIC ACID 1 UNK 0
125894581 12589458 7 C ITRACONAZOLE. ITRACONAZOLE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125894581 12589458 1 Rheumatoid arthritis
125894581 12589458 5 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
125894581 12589458 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125894581 12589458 Alopecia
125894581 12589458 Coccidioidomycosis
125894581 12589458 Cystitis
125894581 12589458 Drug ineffective
125894581 12589458 Fungal infection
125894581 12589458 White blood cell count decreased

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
125894581 12589458 1 20160716 0
125894581 12589458 2 200611 0
125894581 12589458 3 200808 201102 0
125894581 12589458 4 201402 201407 0