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
119778983 11977898 3 F 2007 20160817 20160129 20160825 EXP CA-AMGEN-CANSP2016009711 AMGEN 54.00 YR A F Y 0.00000 20160825 OT CA CA

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
119778983 11977898 1 PS ENBREL ETANERCEPT 1 Subcutaneous UNK U 103795 UNKNOWN FORMULATION
119778983 11977898 2 SS LEFLUNOMIDE. LEFLUNOMIDE 1 Unknown 20 MG, UNK 0 20 MG TABLET
119778983 11977898 3 SS HUMIRA ADALIMUMAB 1 Unknown 40 MG, UNK 0 40 MG
119778983 11977898 4 SS ORENCIA ABATACEPT 1 Unknown UNK 0
119778983 11977898 5 C ARAVA LEFLUNOMIDE 1 UNK 0 TABLET
119778983 11977898 6 C MELOXICAM. MELOXICAM 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119778983 11977898 1 Rheumatoid arthritis
119778983 11977898 2 Rheumatoid arthritis
119778983 11977898 3 Rheumatoid arthritis
119778983 11977898 4 Rheumatoid arthritis
119778983 11977898 5 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
119778983 11977898 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119778983 11977898 Drug ineffective
119778983 11977898 Finger deformity
119778983 11977898 Foot deformity
119778983 11977898 Insomnia
119778983 11977898 Pain
119778983 11977898 Pyrexia
119778983 11977898 Rheumatoid arthritis
119778983 11977898 Swelling

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
119778983 11977898 1 200705 200710 0
119778983 11977898 2 200701 0