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
84867742 8486774 2 F 201203 20160824 20120402 20160831 EXP US-AMGEN-USASP2012019307 AMGEN 59.00 YR A F Y 0.00000 20160831 MD 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
84867742 8486774 1 PS ENBREL ETANERCEPT 1 Unknown 50 MG, QWK Y 1028224 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
84867742 8486774 2 SS ENBREL ETANERCEPT 1 Unknown UNK Y 1067272 103795 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
84867742 8486774 3 C METHOTREXATE. METHOTREXATE 1 1 MG, UNK 0 1 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
84867742 8486774 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
84867742 8486774 OT
84867742 8486774 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
84867742 8486774 Condition aggravated
84867742 8486774 Intervertebral disc protrusion
84867742 8486774 Rheumatoid arthritis
84867742 8486774 Spinal disorder

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
84867742 8486774 1 20100317 20120125 0
84867742 8486774 3 1997 0