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
126966871 12696687 1 I 20160818 20160830 20160830 EXP CA-ORION CORPORATION ORION PHARMA-TREX2016-1456 ORION 49.00 YR F Y 0.00000 20160830 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
126966871 12696687 1 PS METHOTREXATE (TRADE NAME UNKNOWN) METHOTREXATE 1 Unknown U 0
126966871 12696687 2 SS ENBREL ETANERCEPT 1 Subcutaneous U 0
126966871 12696687 3 SS HUMIRA ADALIMUMAB 1 Subcutaneous U 0
126966871 12696687 4 SS PREDNISONE. PREDNISONE 1 Unknown U 0
126966871 12696687 5 SS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) U 0
126966871 12696687 6 C ACTEMRA TOCILIZUMAB 1 Unknown 0
126966871 12696687 7 C CELECOXIB. CELECOXIB 1 Unknown 0
126966871 12696687 8 C HYDROMORPHONE HYDROCHLORIDE. HYDROMORPHONE HYDROCHLORIDE 1 Unknown 0
126966871 12696687 9 C IBUPROFEN. IBUPROFEN 1 Unknown 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126966871 12696687 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126966871 12696687 Drug ineffective
126966871 12696687 Nausea
126966871 12696687 Respiratory disorder
126966871 12696687 Rheumatoid arthritis
126966871 12696687 Type 2 diabetes mellitus

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

no results found

Therapies reported

no results found