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
77270472 7727047 2 F 2008 20130912 20101221 20130930 PER US-AMGEN-TCS406353 AMGEN 39.00 YR F Y 0.00000 20130930 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
77270472 7727047 1 PS Enbrel 1 SUBCUTANEOUS 25 MG, TWICE WEEKLY U 103795 25 MG POWDER AND SOLVENT FOR SOLUTION FOR INJECTION BIW
77270472 7727047 2 SS Enbrel 1 U NOT QUERIED/NOT AVAILABLE 103795 POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
77270472 7727047 3 C METHOTREXATE 1 UNK D 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
77270472 7727047 1 Juvenile idiopathic arthritis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
77270472 7727047 Injection site bruising
77270472 7727047 Injection site discomfort
77270472 7727047 Injection site pain
77270472 7727047 Liver function test abnormal
77270472 7727047 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
77270472 7727047 1 20010101 0
77270472 7727047 3 2008 0