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
70166872 7016687 2 F 20080401 20160801 20090610 20160805 EXP US-AMGEN-QUU349621 AMGEN 60.00 YR A F Y 0.00000 20160805 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
70166872 7016687 1 PS ENBREL ETANERCEPT 1 Subcutaneous 50 MG, QWK U 1006108 103795 50 MG UNKNOWN FORMULATION /wk
70166872 7016687 2 C METHOTREXATE. METHOTREXATE 1 Oral 15 MG, QWK 0 15 MG /wk
70166872 7016687 3 C PREDNISONE. PREDNISONE 1 5 MG, UNK 0 5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
70166872 7016687 1 Rheumatoid arthritis
70166872 7016687 3 Arthritis

Outcome of event

Event ID CASEID OUTC COD
70166872 7016687 OT
70166872 7016687 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
70166872 7016687 Blindness
70166872 7016687 Bronchitis
70166872 7016687 Cough
70166872 7016687 Ear infection
70166872 7016687 Injection site pain
70166872 7016687 Pain
70166872 7016687 Pulmonary cavitation
70166872 7016687 Retinal disorder
70166872 7016687 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
70166872 7016687 1 20040101 0
70166872 7016687 2 19800101 0