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
125973391 12597339 1 I 20160722 20160726 20160726 EXP GB-ABBVIE-16P-167-1685456-00 ABBVIE 55.00 YR M Y 0.00000 20160726 CN GB GB

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
125973391 12597339 1 PS NORVIR RITONAVIR 1 Oral UNKNOWN 20945 100 MG TABLET
125973391 12597339 2 SS ATAZANAVIR ATAZANAVIR 1 Oral 0 300 MG CAPSULE
125973391 12597339 3 SS COTRIMOXAZOLE SULFAMETHOXAZOLETRIMETHOPRIM 1 Oral U 0 TABLET
125973391 12597339 4 SS KIVEXA ABACAVIR SULFATELAMIVUDINE 1 Oral U 0 TABLET
125973391 12597339 5 SS DOLUTEGRAVIR DOLUTEGRAVIR 1 Oral U 0 50 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125973391 12597339 1 Product used for unknown indication
125973391 12597339 2 Product used for unknown indication
125973391 12597339 3 Product used for unknown indication
125973391 12597339 4 Product used for unknown indication
125973391 12597339 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125973391 12597339 DE
125973391 12597339 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125973391 12597339 Death

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

no results found

Therapies reported

no results found