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
122130983 12213098 3 F 20160822 20160328 20160825 EXP CA-AMGEN-CANSP2016035723 AMGEN 66.00 YR E F Y 0.00000 20160825 OT 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
122130983 12213098 1 PS ENBREL ETANERCEPT 1 Subcutaneous UNK U 103795 UNKNOWN FORMULATION
122130983 12213098 2 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Oral UNK 0
122130983 12213098 3 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown UNK 0 TABLET
122130983 12213098 4 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) UNK 0 POWDER AND SOLVENT FOR SOLUTION FOR INFUSION
122130983 12213098 5 SS XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, BID, 5 MG, 2 EVERY 1 DAY 0 5 MG TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122130983 12213098 1 Rheumatoid arthritis
122130983 12213098 2 Rheumatoid arthritis
122130983 12213098 3 Rheumatoid arthritis
122130983 12213098 4 Rheumatoid arthritis
122130983 12213098 5 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
122130983 12213098 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122130983 12213098 Drug ineffective
122130983 12213098 Pain in extremity
122130983 12213098 Peripheral swelling

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

no results found

Therapies reported

no results found