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
126260591 12626059 1 I 20160721 20160805 20160805 EXP E2B_00506460 CA-HQ SPECIALTY-CA-2016INT000700 INTERCHEM 0.00 F Y 0.00000 20160805 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
126260591 12626059 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 UNK U 201749
126260591 12626059 2 SS ENBREL ETANERCEPT 1 Subcutaneous UNK U 0
126260591 12626059 3 SS ACTEMRA TOCILIZUMAB 1 UNK U 0
126260591 12626059 4 SS CIMZIA CERTOLIZUMAB PEGOL 1 Subcutaneous UNK U 0
126260591 12626059 5 SS FOLIC ACID. FOLIC ACID 1 UNK U 0
126260591 12626059 6 SS FOSAMAX ALENDRONATE SODIUM 1 UNK U 0
126260591 12626059 7 SS HUMIRA ADALIMUMAB 1 Subcutaneous UNK U 0
126260591 12626059 8 SS ORENCIA ABATACEPT 1 Intravenous (not otherwise specified) UNK U 0
126260591 12626059 9 SS PHTHALYLSULFATHIAZOLE PHTHALYLSULFATHIAZOLE 1 UNK U 0
126260591 12626059 10 SS PLAQUENIL /00072602/ HYDROXYCHLOROQUINE DIPHOSPHATE 1 UNK U 0
126260591 12626059 11 SS PREDNISONE. PREDNISONE 1 UNK U 0
126260591 12626059 12 SS REACTINE /00884302/ CETIRIZINE HYDROCHLORIDE 1 UNK U 0
126260591 12626059 13 SS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) UNK U 0
126260591 12626059 14 SS SIMPONI GOLIMUMAB 1 Subcutaneous UNK U 0
126260591 12626059 15 SS ARAVA LEFLUNOMIDE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126260591 12626059 1 Product used for unknown indication
126260591 12626059 2 Product used for unknown indication
126260591 12626059 3 Product used for unknown indication
126260591 12626059 4 Product used for unknown indication
126260591 12626059 5 Product used for unknown indication
126260591 12626059 6 Product used for unknown indication
126260591 12626059 7 Product used for unknown indication
126260591 12626059 8 Product used for unknown indication
126260591 12626059 9 Product used for unknown indication
126260591 12626059 10 Product used for unknown indication
126260591 12626059 11 Product used for unknown indication
126260591 12626059 12 Product used for unknown indication
126260591 12626059 13 Product used for unknown indication
126260591 12626059 14 Rheumatoid arthritis
126260591 12626059 15 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126260591 12626059 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126260591 12626059 Abdominal discomfort
126260591 12626059 Alopecia
126260591 12626059 Glossodynia
126260591 12626059 Hip arthroplasty
126260591 12626059 Knee arthroplasty
126260591 12626059 Maternal exposure during pregnancy
126260591 12626059 Pain
126260591 12626059 Pemphigus
126260591 12626059 Rheumatoid arthritis
126260591 12626059 Systemic lupus erythematosus

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

no results found

Therapies reported

no results found