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
968487813 9684878 13 F 2013 20160818 20131112 20160822 EXP CA-ROCHE-1183959 ROCHE 48.54 YR F Y 116.00000 KG 20160822 OT 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
968487813 9684878 1 PS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) U B20151,B20192,B2034 125276 800 MG SOLUTION FOR INFUSION
968487813 9684878 2 SS ACTEMRA TOCILIZUMAB 1 Subcutaneous WEEKLY 125472 162 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
968487813 9684878 3 SS NAPROSYN NAPROXEN 1 Unknown U 17581
968487813 9684878 4 SS METHOTREXATE. METHOTREXATE 1 Oral U 0 20 MG /wk
968487813 9684878 5 C CLONAZEPAM. CLONAZEPAM 1 0
968487813 9684878 6 C ATENOLOL. ATENOLOL 1 0
968487813 9684878 7 C LYRICA PREGABALIN 1 0
968487813 9684878 8 C FOLIC ACID. FOLIC ACID 1 0
968487813 9684878 9 C GLUCOSAMINE SULFATE GLUCOSAMINE SULFATE 1 0
968487813 9684878 10 C CYMBALTA DULOXETINE HYDROCHLORIDE 1 0
968487813 9684878 11 C PERCOCET ACETAMINOPHENOXYCODONE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
968487813 9684878 1 Rheumatoid arthritis
968487813 9684878 2 Rheumatoid arthritis
968487813 9684878 3 Product used for unknown indication
968487813 9684878 4 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
968487813 9684878 OT
968487813 9684878 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
968487813 9684878 Arthralgia
968487813 9684878 Blood bilirubin increased
968487813 9684878 Drug ineffective
968487813 9684878 Dyskinesia
968487813 9684878 Fatigue
968487813 9684878 Feeling cold
968487813 9684878 Fibromyalgia
968487813 9684878 Intervertebral disc protrusion
968487813 9684878 Liver function test increased
968487813 9684878 Musculoskeletal stiffness
968487813 9684878 Nephrolithiasis
968487813 9684878 Otitis media
968487813 9684878 Pain
968487813 9684878 Pustular psoriasis
968487813 9684878 Restless legs syndrome
968487813 9684878 Rheumatoid arthritis
968487813 9684878 Swelling
968487813 9684878 Upper respiratory tract infection
968487813 9684878 Urinary tract infection
968487813 9684878 Weight abnormal
968487813 9684878 Weight increased

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
968487813 9684878 1 20121214 20140729 0
968487813 9684878 2 20140826 0
968487813 9684878 4 201402 0