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
125798371 12579837 1 I 20160714 20160721 20160721 EXP CA-PFIZER INC-2016355316 PFIZER 0.00 F Y 0.00000 20160721 MD 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
125798371 12579837 1 SS ENBREL ETANERCEPT 1 UNK U 0 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
125798371 12579837 2 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 20 MG, QWK U 11719 20 MG /wk
125798371 12579837 3 SS HUMIRA ADALIMUMAB 1 Subcutaneous UNK U 0
125798371 12579837 4 SS LEFLUNOMIDE. LEFLUNOMIDE 1 Unknown UNK, DAILY U 0 TABLET
125798371 12579837 5 SS ORENCIA ABATACEPT 1 UNK U 0
125798371 12579837 6 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown 400 MG, QD U 0 400 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125798371 12579837 3 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
125798371 12579837 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125798371 12579837 Activities of daily living impaired
125798371 12579837 Bone erosion
125798371 12579837 Drug hypersensitivity
125798371 12579837 Drug ineffective
125798371 12579837 Drug intolerance
125798371 12579837 Gastric ulcer
125798371 12579837 Inflammation
125798371 12579837 Pain
125798371 12579837 Rheumatoid arthritis
125798371 12579837 Rheumatoid factor positive
125798371 12579837 Synovitis

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

no results found

Therapies reported

no results found