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
126892071 12689207 1 I 20160818 20160826 20160826 EXP CA-ORION CORPORATION ORION PHARMA-TREX2016-1434 ORION 62.00 YR F Y 0.00000 20160826 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
126892071 12689207 1 PS METHOTREXATE (TRADE NAME UNKNOWN) METHOTREXATE 1 Unknown U 0
126892071 12689207 2 SS ENBREL ETANERCEPT 1 Subcutaneous U 0
126892071 12689207 3 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) U 0
126892071 12689207 4 SS ACTEMRA TOCILIZUMAB 1 Unknown U 0
126892071 12689207 5 SS ARAVA LEFLUNOMIDE 1 Unknown U 0 TABLET
126892071 12689207 6 SS CICLOSPORIN CYCLOSPORINE 1 Unknown U 0
126892071 12689207 7 SS IMURAN AZATHIOPRINE 1 Unknown U 0
126892071 12689207 8 SS ORENCIA ABATACEPT 1 Intravenous (not otherwise specified) U 0
126892071 12689207 9 SS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) U 0
126892071 12689207 10 SS SODIUM AUROTHIOMALATE GOLD SODIUM THIOMALATE 1 Intramuscular U 0 INJECTION

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126892071 12689207 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126892071 12689207 Demyelination
126892071 12689207 Diabetes mellitus
126892071 12689207 Drug hypersensitivity
126892071 12689207 Impaired gastric emptying
126892071 12689207 Renal impairment
126892071 12689207 Rheumatoid arthritis
126892071 12689207 Therapeutic response decreased

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

no results found

Therapies reported

no results found