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
122021145 12202114 5 F 2016 20160830 20160322 20160914 PER US-AMGEN-USASL2016034196 AMGEN 55.00 YR A F Y 0.00000 20160914 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
122021145 12202114 1 PS ENBREL ETANERCEPT 1 Unknown 50 MG, QWK U 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
122021145 12202114 2 SS PREDNISONE. PREDNISONE 1 Unknown 40 MG, UNK 0 40 MG
122021145 12202114 3 SS PREDNISONE. PREDNISONE 1 Unknown 20 MG, UNK 0 20 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122021145 12202114 1 Rheumatoid arthritis
122021145 12202114 2 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
122021145 12202114 Eye irritation
122021145 12202114 Generalised oedema
122021145 12202114 Headache
122021145 12202114 Impaired work ability
122021145 12202114 Influenza like illness
122021145 12202114 Musculoskeletal disorder
122021145 12202114 Musculoskeletal stiffness
122021145 12202114 Nasopharyngitis
122021145 12202114 Oropharyngeal pain
122021145 12202114 Pain
122021145 12202114 Peripheral swelling
122021145 12202114 Sinusitis
122021145 12202114 Throat irritation

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
122021145 12202114 1 201602 0