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
118400787 11840078 7 F 20150512 20160727 20151216 20160728 EXP CA-ROCHE-1578083 ROCHE 65.67 YR M Y 0.00000 20160728 MD 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
118400787 11840078 1 PS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 674 MG SOLUTION FOR INFUSION
118400787 11840078 2 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 680 MG SOLUTION FOR INFUSION
118400787 11840078 3 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 656 MG SOLUTION FOR INFUSION
118400787 11840078 4 C SULPHASALAZINE SULFASALAZINE 1 0
118400787 11840078 5 C NAPROXEN. NAPROXEN 1 0
118400787 11840078 6 C METHOTREXATE. METHOTREXATE 1 0
118400787 11840078 7 C TELMISARTAN. TELMISARTAN 1 0
118400787 11840078 8 C ZANTAC RANITIDINE HYDROCHLORIDE 1 0
118400787 11840078 9 C RAPAFLO SILODOSIN 1 0
118400787 11840078 10 C PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118400787 11840078 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
118400787 11840078 LT
118400787 11840078 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
118400787 11840078 Arthralgia
118400787 11840078 Bladder neoplasm
118400787 11840078 Blood pressure diastolic decreased
118400787 11840078 Blood pressure fluctuation
118400787 11840078 Blood urine present
118400787 11840078 Cerebrovascular accident
118400787 11840078 Drug ineffective
118400787 11840078 Haematoma
118400787 11840078 Hypotension
118400787 11840078 Joint swelling
118400787 11840078 No adverse event
118400787 11840078 Oxygen saturation decreased
118400787 11840078 Pain
118400787 11840078 Pain in extremity

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
118400787 11840078 1 20150512 0
118400787 11840078 2 20150609 0
118400787 11840078 3 20160506 20160711 0