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
99274913 9927491 3 F 20130905 20160721 20140227 20160727 EXP BR-AMGEN-BRASP2013064549 AMGEN 58.00 YR A F Y 78.00000 KG 20160727 OT BR BR

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
99274913 9927491 1 PS ENBREL ETANERCEPT 1 Subcutaneous 50 MG, ONCE WEEKLY 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
99274913 9927491 2 C PARACETAMOL ACETAMINOPHEN 1 UNK, AS NEEDED 0
99274913 9927491 3 C TECNOMET /00113801/ METHOTREXATE 1 UNK, QWK 0 /wk
99274913 9927491 4 C TECNOMET /00113801/ METHOTREXATE 1 5 DF, WEEKLY 0
99274913 9927491 5 C VENLAFAXINE VENLAFAXINE HYDROCHLORIDE 1 STRENGTH 150 MG 0
99274913 9927491 6 C VENLAFAXINE VENLAFAXINE HYDROCHLORIDE 1 150 MG, DAILY 0 150 MG
99274913 9927491 7 C NIMESULIDE NIMESULIDE 1 UNK, AS NEEDED 0
99274913 9927491 8 C FOLIC ACID. FOLIC ACID 1 1 DF, WEEKLY 0 1 DF /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
99274913 9927491 1 Rheumatoid arthritis
99274913 9927491 2 Pain
99274913 9927491 3 Arthritis
99274913 9927491 7 Pain

Outcome of event

Event ID CASEID OUTC COD
99274913 9927491 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
99274913 9927491 Arthropathy
99274913 9927491 Injection site erythema

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
99274913 9927491 1 201304 0