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
113185722 11318572 2 F 20160705 20160705 20150729 20160708 PER US-AMGEN-USASP2015072070 AMGEN 68.00 YR E F Y 0.00000 20160708 CN 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
113185722 11318572 1 PS ENBREL ETANERCEPT 1 Unknown 50 MG, QWK U 1055192 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
113185722 11318572 2 SS ENBREL ETANERCEPT 1 U 103795 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113185722 11318572 1 Rheumatoid arthritis
113185722 11318572 2 Osteoarthritis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
113185722 11318572 Device difficult to use
113185722 11318572 Device malfunction
113185722 11318572 Headache
113185722 11318572 Incorrect dosage administered
113185722 11318572 Incorrect product storage
113185722 11318572 Injection site erythema
113185722 11318572 Injection site rash
113185722 11318572 Injury associated with device
113185722 11318572 Wrong technique in product usage process

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found