The Safety Rates Drug Report

Member Login
2004.Q1    2004.Q2    2004.Q3    2004.Q4    2005.Q1    2005.Q2    2005.Q3    2005.Q4    2006.Q1    2006.Q2    2006.Q3    2006.Q4    2007.Q1    2007.Q2    2007.Q3    2007.Q4    2008.Q1    2008.Q2    2008.Q3    2008.Q4    2009.Q1    2009.Q2    2009.Q3    2009.Q4    2010.Q1    2010.Q2    2010.Q3    2010.Q4    2011.Q1    2011.Q2    2011.Q3    2011.Q4    2012.Q1    2012.Q2    2012.Q3    2012.Q4    2013.Q1    2013.Q2    2013.Q3    2013.Q4    2014.Q1    2014.Q2    2014.Q3    2014.Q4    2015.Q1    2015.Q2    2015.Q3    2015.Q4    2016.Q1    2016.Q2    2016.Q3   

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
126992631 12699263 1 I 20150923 20160830 20160830 EXP CA-CONCORDIA PHARMACEUTICALS INC.-CO-PL-CA-2016-444 CONCORDIA 43.00 YR F Y 0.00000 20160829 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
126992631 12699263 1 PS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown 0 400 MG QD
126992631 12699263 2 SS ARAVA LEFLUNOMIDE 1 0
126992631 12699263 3 SS ENBREL ETANERCEPT 1 Subcutaneous 0
126992631 12699263 4 SS METHOTREXATE. METHOTREXATE 1 Oral 0 25 MG
126992631 12699263 5 SS CORTISONE CORTISONEHYDROCORTISONE 1 Oral 0
126992631 12699263 6 SS FOLIC ACID. FOLIC ACID 1 0
126992631 12699263 7 SS PREDNISONE. PREDNISONE 1 0
126992631 12699263 8 SS SULFATHALIDINE PHTHALYLSULFATHIAZOLE 1 0
126992631 12699263 9 SS SULFASALAZINE. SULFASALAZINE 1 Oral 0 1 G BID
126992631 12699263 10 SS REMICADE INFLIXIMAB 1 0
126992631 12699263 11 SS ACTEMRA TOCILIZUMAB 1 0
126992631 12699263 12 SS ORENCIA ABATACEPT 1 Intravenous (not otherwise specified) 0
126992631 12699263 13 SS CIMZIA CERTOLIZUMAB PEGOL 1 Subcutaneous 0
126992631 12699263 14 SS HUMIRA ADALIMUMAB 1 Subcutaneous 0
126992631 12699263 15 SS RITUXAN RITUXIMAB 1 0
126992631 12699263 16 SS SIMPONI GOLIMUMAB 1 Subcutaneous 0
126992631 12699263 17 SS REACTINE CETIRIZINE HYDROCHLORIDE 1 0
126992631 12699263 18 SS FOSAMAX ALENDRONATE SODIUM 1 0
126992631 12699263 19 C XELJANZ TOFACITINIB CITRATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126992631 12699263 1 Product used for unknown indication
126992631 12699263 3 Rheumatoid arthritis
126992631 12699263 4 Rheumatoid arthritis
126992631 12699263 5 Rheumatoid arthritis
126992631 12699263 6 Rheumatoid arthritis
126992631 12699263 7 Rheumatoid arthritis
126992631 12699263 9 Rheumatoid arthritis
126992631 12699263 10 Rheumatoid arthritis
126992631 12699263 11 Rheumatoid arthritis
126992631 12699263 12 Rheumatoid arthritis
126992631 12699263 13 Rheumatoid arthritis
126992631 12699263 14 Rheumatoid arthritis
126992631 12699263 15 Rheumatoid arthritis
126992631 12699263 16 Rheumatoid arthritis
126992631 12699263 17 Rheumatoid arthritis
126992631 12699263 18 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
126992631 12699263 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126992631 12699263 Abdominal discomfort
126992631 12699263 Alopecia
126992631 12699263 Glossodynia
126992631 12699263 Pain
126992631 12699263 Pemphigus
126992631 12699263 Systemic lupus erythematosus

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
126992631 12699263 1 2006 0
126992631 12699263 4 2006 0
126992631 12699263 9 2006 2007 0
126992631 12699263 12 20100510 201103 0
126992631 12699263 15 2009 2010 0