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 CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
8480329 8439903 F 8480329-0 20110601 20120621 20120630 EXP DK-TEVA-324463ISR TEVA 61 YR F Y 88 KG 20120630 MD DENMARK

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
8480329 1020135229 C FOLIC ACID 1
8480329 1020135228 SS HUMIRA 1
8480329 1020135227 PS METHOTREXATE 1 ORAL 081099

Indications of drugs used

Event ID DRUG SEQ INDI PT
8480329 1020135228 PSORIATIC ARTHROPATHY
8480329 1020135227 PSORIATIC ARTHROPATHY

Outcome of event

Event ID OUTC COD
8480329 HO

Reactions reported

Event ID PT
8480329 UTERINE CANCER

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
8480329 1020135228 20070430 20110523
8480329 1020135227 20070403 20110405