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
126001662 12600166 2 F 2016 20160831 20160727 20160920 PER US-AMGEN-USASL2016094842 AMGEN 63.00 YR A F Y 0.00000 20160920 CN US US

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
126001662 12600166 1 PS ENBREL ETANERCEPT 1 Unknown UNK U 103795 UNKNOWN FORMULATION
126001662 12600166 2 SS ENBREL ETANERCEPT 1 Unknown 50 MG, QWK U 1064421 103795 50 MG UNKNOWN FORMULATION /wk
126001662 12600166 3 SS ORENCIA ABATACEPT 1 Unknown UNK 0
126001662 12600166 4 SS XELJANZ TOFACITINIB CITRATE 1 Unknown UNK 0
126001662 12600166 5 C RASUVO METHOTREXATE SODIUM 1 15 MG, QWK EVERY FRIDAY 0 15 MG /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126001662 12600166 1 Rheumatoid arthritis
126001662 12600166 3 Product used for unknown indication
126001662 12600166 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126001662 12600166 Injection site pain
126001662 12600166 Malaise
126001662 12600166 Sinusitis

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
126001662 12600166 2 201605 0