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
118046902 11804690 2 F 20151020 20160622 20151205 20160702 EXP GB-AMGEN-GBRSP2015113410 AMGEN 61.00 YR A F Y 0.00000 20160701 CN GB GB

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
118046902 11804690 1 PS ENBREL ETANERCEPT 1 Subcutaneous 50 MG, WEEKLY Y 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
118046902 11804690 2 C METHOTREXATE. METHOTREXATE 1 25 MG, UNK 0 25 MG
118046902 11804690 3 C HYDROXYCHLOROQUINE HYDROXYCHLOROQUINE 1 10 MG, UNK 0 10 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118046902 11804690 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
118046902 11804690 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
118046902 11804690 Condition aggravated
118046902 11804690 Injection site pruritus
118046902 11804690 Injection site swelling
118046902 11804690 Nasopharyngitis
118046902 11804690 Rheumatoid arthritis

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
118046902 11804690 1 20151020 0