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
104060592 10406059 2 F 20140805 20160321 20140825 20160331 PER US-AMGEN INC.-USASP2014063209 AMGEN 57.00 YR A F Y 0.00000 20160331 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
104060592 10406059 1 PS ENBREL ETANERCEPT 1 Unknown 50 MG, QWK 1047371 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
104060592 10406059 2 SS ENBREL ETANERCEPT 1 Unknown UNK 1062647 103795 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
104060592 10406059 1 Rheumatoid arthritis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
104060592 10406059 Arthritis
104060592 10406059 Device issue
104060592 10406059 Dizziness
104060592 10406059 Injection site erythema
104060592 10406059 Injection site irritation
104060592 10406059 Injection site pain
104060592 10406059 Injection site pruritus
104060592 10406059 Injection site rash
104060592 10406059 Injection site recall reaction
104060592 10406059 Photophobia
104060592 10406059 Vision blurred

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
104060592 10406059 1 20140802 0