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
125829001 12582900 1 I 20160712 20160722 20160722 EXP CA-PFIZER INC-2016351024 PFIZER 54.00 YR F Y 0.00000 20160722 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
125829001 12582900 1 SS ENBREL ETANERCEPT 1 Subcutaneous UNK U 0
125829001 12582900 2 PS CELEBREX CELECOXIB 1 UNK U 20998 CAPSULE, HARD
125829001 12582900 3 SS XELJANZ TOFACITINIB CITRATE 1 Oral 10 ML, UNK U 203214 10 ML TABLET BID
125829001 12582900 4 SS XELJANZ TOFACITINIB CITRATE 1 Oral 5 ML, 2X/DAY U 203214 5 ML TABLET BID
125829001 12582900 5 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 UNK U 11719
125829001 12582900 6 SS HUMIRA ADALIMUMAB 1 Subcutaneous UNK U 0
125829001 12582900 7 SS RITUXAN RITUXIMAB 1 Intravesical UNK U 0
125829001 12582900 8 SS SIMPONI GOLIMUMAB 1 Subcutaneous UNK U 0
125829001 12582900 9 SS VIOXX ROFECOXIB 1 UNK U 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125829001 12582900 2 Rheumatoid arthritis
125829001 12582900 5 Rheumatoid arthritis
125829001 12582900 6 Rheumatoid arthritis
125829001 12582900 7 Rheumatoid arthritis
125829001 12582900 8 Rheumatoid arthritis
125829001 12582900 9 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
125829001 12582900 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125829001 12582900 Drug ineffective
125829001 12582900 Nasopharyngitis
125829001 12582900 Rheumatoid arthritis
125829001 12582900 Stress

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found