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
125241001 12524100 1 I 201606 20160627 20160704 20160704 PER US-AMGEN-USASP2016083688 AMGEN 53.00 YR A F Y 0.00000 20160704 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
125241001 12524100 1 PS ENBREL ETANERCEPT 1 Unknown 50 MG, QWK U 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
125241001 12524100 2 SS AMOXICILLIN. AMOXICILLIN 1 Unknown UNK 0
125241001 12524100 3 SS AMOXICILLIN. AMOXICILLIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125241001 12524100 1 Rheumatoid arthritis
125241001 12524100 2 Nasopharyngitis
125241001 12524100 3 Secretion discharge

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125241001 12524100 Diarrhoea
125241001 12524100 Fatigue
125241001 12524100 Malaise
125241001 12524100 Nasopharyngitis
125241001 12524100 Secretion discharge
125241001 12524100 Sputum discoloured

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
125241001 12524100 1 2011 0