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
117580543 11758054 3 F 201307 20160714 20151120 20160719 EXP CA-AMGEN-CANSP2015122252 AMGEN 47.00 YR A F Y 0.00000 20160719 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
117580543 11758054 1 PS ENBREL ETANERCEPT 1 Unknown UNK 103795 UNKNOWN FORMULATION
117580543 11758054 2 SS METHOTREXATE (METHOTREXATE SODIUM) METHOTREXATE SODIUM 1 Unknown UNK 0
117580543 11758054 3 C CELEBREX CELECOXIB 1 UNK 0
117580543 11758054 4 C ARAVA LEFLUNOMIDE 1 UNK 0
117580543 11758054 5 C ORENCIA ABATACEPT 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117580543 11758054 1 Rheumatoid arthritis
117580543 11758054 2 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
117580543 11758054 HO
117580543 11758054 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
117580543 11758054 Arthralgia
117580543 11758054 Drug effect decreased
117580543 11758054 Influenza like illness
117580543 11758054 Joint swelling
117580543 11758054 Knee arthroplasty
117580543 11758054 Localised infection
117580543 11758054 Musculoskeletal pain
117580543 11758054 Nausea
117580543 11758054 Staphylococcal infection
117580543 11758054 Therapeutic response decreased
117580543 11758054 Vomiting

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
117580543 11758054 2 1997 0