The Safety Rates Drug Report

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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
117763212 11776321 2 F 20160714 20151125 20160719 EXP CA-AMGEN-CANSP2015124500 AMGEN 58.00 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
117763212 11776321 1 PS ENBREL ETANERCEPT 1 Unknown UNK U 103795 UNKNOWN FORMULATION
117763212 11776321 2 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Unknown UNK 0
117763212 11776321 3 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown 400 MG, BID 0 400 MG TABLET BID
117763212 11776321 4 C HUMIRA ADALIMUMAB 1 UNK 0
117763212 11776321 5 C ORENCIA ABATACEPT 1 UNK 0
117763212 11776321 6 C RITUXAN RITUXIMAB 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117763212 11776321 1 Rheumatoid arthritis
117763212 11776321 2 Rheumatoid arthritis
117763212 11776321 3 Rheumatoid arthritis
117763212 11776321 4 Rheumatoid arthritis
117763212 11776321 5 Rheumatoid arthritis
117763212 11776321 6 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
117763212 11776321 DS
117763212 11776321 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
117763212 11776321 Disability
117763212 11776321 Drug ineffective
117763212 11776321 Eye disorder
117763212 11776321 Rash
117763212 11776321 Rheumatoid arthritis

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found