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
125685331 12568533 1 I 20160712 20160719 20160719 EXP CA-AMGEN-CANSP2016091465 AMGEN 0.00 F Y 0.00000 20160718 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
125685331 12568533 1 PS ENBREL ETANERCEPT 1 Subcutaneous UNK U 103795 UNKNOWN FORMULATION
125685331 12568533 2 SS ACTEMRA TOCILIZUMAB 1 Unknown UNK 0
125685331 12568533 3 SS ARAVA LEFLUNOMIDE 1 Unknown UNK 0 TABLET
125685331 12568533 4 SS CIMZIA CERTOLIZUMAB PEGOL 1 Subcutaneous UNK 0
125685331 12568533 5 SS FOLIC ACID. FOLIC ACID 1 Unknown UNK 0
125685331 12568533 6 SS FOSAMAX ALENDRONATE SODIUM 1 Unknown UNK 0 TABLET
125685331 12568533 7 SS HUMIRA ADALIMUMAB 1 Subcutaneous UNK 0
125685331 12568533 8 SS METHOTREXATE. METHOTREXATE 1 Unknown UNK 0
125685331 12568533 9 SS ORENCIA ABATACEPT 1 Intravenous (not otherwise specified) UNK 0
125685331 12568533 10 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown UNK 0 TABLET
125685331 12568533 11 SS PREDNISONE. PREDNISONE 1 Unknown UNK 0
125685331 12568533 12 SS REACTINE CETIRIZINE HYDROCHLORIDE 1 Unknown UNK 0
125685331 12568533 13 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) UNK 0
125685331 12568533 14 SS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) UNK 0
125685331 12568533 15 SS SIMPONI GOLIMUMAB 1 Subcutaneous UNK 0
125685331 12568533 16 SS SULFASALAZINE. SULFASALAZINE 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125685331 12568533 1 Rheumatoid arthritis
125685331 12568533 2 Rheumatoid arthritis
125685331 12568533 3 Rheumatoid arthritis
125685331 12568533 4 Rheumatoid arthritis
125685331 12568533 5 Product used for unknown indication
125685331 12568533 6 Rheumatoid arthritis
125685331 12568533 7 Rheumatoid arthritis
125685331 12568533 8 Rheumatoid arthritis
125685331 12568533 9 Rheumatoid arthritis
125685331 12568533 10 Rheumatoid arthritis
125685331 12568533 11 Rheumatoid arthritis
125685331 12568533 12 Product used for unknown indication
125685331 12568533 13 Rheumatoid arthritis
125685331 12568533 14 Rheumatoid arthritis
125685331 12568533 15 Rheumatoid arthritis
125685331 12568533 16 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
125685331 12568533 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125685331 12568533 Abdominal discomfort
125685331 12568533 Alopecia
125685331 12568533 Fatigue
125685331 12568533 Glossodynia
125685331 12568533 Hand deformity
125685331 12568533 Hip arthroplasty
125685331 12568533 Knee arthroplasty
125685331 12568533 Pain
125685331 12568533 Pemphigus
125685331 12568533 Swelling
125685331 12568533 Systemic lupus erythematosus
125685331 12568533 Wound

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

no results found

Therapies reported

no results found