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
115958094 11595809 4 F 20160907 20151006 20160912 EXP CA-ROCHE-1641281 ROCHE 56.00 YR F Y 0.00000 20160912 CN 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
115958094 11595809 1 PS ACTEMRA TOCILIZUMAB 1 Unknown 125276
115958094 11595809 2 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Unknown U 0
115958094 11595809 3 SS HUMIRA ADALIMUMAB 1 Subcutaneous U 0
115958094 11595809 4 SS ENBREL ETANERCEPT 1 Subcutaneous U 0
115958094 11595809 5 C FOLIC ACID. FOLIC ACID 1 0
115958094 11595809 6 C INDOMETHACIN. INDOMETHACIN 1 0
115958094 11595809 7 C XELJANZ TOFACITINIB CITRATE 1 Oral 0 5 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115958094 11595809 1 Rheumatoid arthritis
115958094 11595809 2 Rheumatoid arthritis
115958094 11595809 3 Rheumatoid arthritis
115958094 11595809 4 Rheumatoid arthritis
115958094 11595809 7 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
115958094 11595809 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
115958094 11595809 Arthralgia
115958094 11595809 Arthropathy
115958094 11595809 Drug ineffective
115958094 11595809 Dysstasia
115958094 11595809 Fall
115958094 11595809 Fine motor skill dysfunction
115958094 11595809 Gait disturbance
115958094 11595809 Mobility decreased
115958094 11595809 Seizure

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
115958094 11595809 4 2013 0