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
77173752 7717375 2 F 20101105 20120326 20101217 20160707 EXP BR-AMGEN-BRASP2010008643 AMGEN 0.00 F Y 56.00000 KG 20160706 CN BR BR

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
77173752 7717375 1 PS ENBREL ETANERCEPT 1 Subcutaneous 50 MG, WEEKLY 103795 50 MG POWDER AND SOLVENT FOR SOLUTION FOR INJECTION /wk
77173752 7717375 2 C PREDNISONE. PREDNISONE 1 5 MG, 1 TABLET IN THE MORNING 0 5 MG
77173752 7717375 3 C METHOTREXATE. METHOTREXATE 1 Intramuscular UNK UNK, WEEKLY 0 /wk
77173752 7717375 4 C ARAVA LEFLUNOMIDE 1 20 MG, UNK, 1 TABLET IN THE MORNING 0 20 MG
77173752 7717375 5 C CICLOSPORIN CYCLOSPORINE 1 UNK 0
77173752 7717375 6 C CHLOROQUINE. CHLOROQUINE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
77173752 7717375 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
77173752 7717375 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
77173752 7717375 Accident
77173752 7717375 Injection site erythema
77173752 7717375 Injection site hypersensitivity
77173752 7717375 Injection site pruritus
77173752 7717375 Lower limb fracture

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
77173752 7717375 1 20100917 0