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
122357072 12235707 2 F 20160729 20160404 20160812 EXP 2015M1010089 CA-HQ SPECIALTY-CA-2016INT000158 INTERCHEM 61.00 YR F Y 0.00000 20160812 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
122357072 12235707 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Unknown 3.5714 MG (25 MG,1 IN 1 W) 201749
122357072 12235707 2 SS ARAVA LEFLUNOMIDE 1 Unknown (20 MG,1 D) N 0
122357072 12235707 3 SS REMICADE INFLIXIMAB 1 Unknown 5.3571 MG (300 MG,1 IN 8 W) N 0
122357072 12235707 4 SS RITUXAN RITUXIMAB 1 Unknown UNK N 0
122357072 12235707 5 SS XELJANZ TOFACITINIB CITRATE 1 Oral 10 MG (5 MG, 2 IN 1 D) 0
122357072 12235707 6 SS ACTEMRA TOCILIZUMAB 1 Unknown (8 MG/KG) N 0
122357072 12235707 7 SS CIMZIA CERTOLIZUMAB PEGOL 1 Unknown (200 MG) N 0
122357072 12235707 8 SS ORENCIA ABATACEPT 1 Unknown 25 MG (750 MG,1 IN 1 MO) N 0
122357072 12235707 9 SS SIMPONI GOLIMUMAB 1 Unknown 1.6667 MG (50 MG,1 IN 1 MO) N 0
122357072 12235707 10 C INSULIN INSULIN NOS 1 Oral UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122357072 12235707 1 Rheumatoid arthritis
122357072 12235707 2 Rheumatoid arthritis
122357072 12235707 3 Rheumatoid arthritis
122357072 12235707 4 Rheumatoid arthritis
122357072 12235707 5 Rheumatoid arthritis
122357072 12235707 6 Product used for unknown indication
122357072 12235707 7 Product used for unknown indication
122357072 12235707 8 Product used for unknown indication
122357072 12235707 9 Product used for unknown indication
122357072 12235707 10 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
122357072 12235707 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122357072 12235707 Drug ineffective
122357072 12235707 Headache
122357072 12235707 Insomnia
122357072 12235707 Memory impairment
122357072 12235707 Pain
122357072 12235707 Swelling

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
122357072 12235707 1 200902 0
122357072 12235707 2 200907 201102 0
122357072 12235707 3 201002 201103 0
122357072 12235707 4 2014 0
122357072 12235707 5 20150331 0
122357072 12235707 6 201108 201111 0
122357072 12235707 7 20110913 201202 0
122357072 12235707 8 20120308 20150902 0
122357072 12235707 9 201305 20131209 0