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
127099172 12709917 2 F 201608 20160831 20160901 20160907 PER US-AMGEN-USASL2016112719 AMGEN 57.00 YR A F Y 0.00000 20160907 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
127099172 12709917 1 PS ENBREL ETANERCEPT 1 Unknown 50 MG, QWK U 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
127099172 12709917 2 SS PREDNISONE. PREDNISONE 1 Unknown 5 MG, QD 0 5 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127099172 12709917 1 Rheumatoid arthritis
127099172 12709917 2 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127099172 12709917 Arthralgia
127099172 12709917 Arthritis
127099172 12709917 Back pain
127099172 12709917 Drug effect incomplete
127099172 12709917 Injection site bruising
127099172 12709917 Nasal congestion
127099172 12709917 Nausea
127099172 12709917 Pain in extremity
127099172 12709917 Peripheral swelling

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
127099172 12709917 1 20160811 0
127099172 12709917 2 201608 20160830 0