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
125510021 12551002 1 I 20160622 20160705 20160713 20160713 EXP GB-BAXTER-2016BAX035829 BAXTER 67.00 YR M Y 0.00000 20160712 OT 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
125510021 12551002 1 PS METRONIDAZOLE 500 MG / 100 ML INTRAVENOUS INFUSION METRONIDAZOLE 1 Unknown U U 0 SOLUTION FOR INFUSION
125510021 12551002 2 SS Clexane ENOXAPARIN SODIUM 1 Unknown U U 0
125510021 12551002 3 SS Atorvastin ATORVASTATIN 1 Unknown U U 0
125510021 12551002 4 SS EZETIMIBE. EZETIMIBE 1 Oral U U 0 TABLET
125510021 12551002 5 SS insulin INSULIN NOS 1 Unknown U U 0
125510021 12551002 6 SS OMEPRAZOLE. OMEPRAZOLE 1 Oral U U 0 CAPSULE
125510021 12551002 7 SS RAMIPRIL. RAMIPRIL 1 Unknown U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125510021 12551002 1 Product used for unknown indication
125510021 12551002 2 Product used for unknown indication
125510021 12551002 3 Product used for unknown indication
125510021 12551002 4 Product used for unknown indication
125510021 12551002 5 Product used for unknown indication
125510021 12551002 6 Product used for unknown indication
125510021 12551002 7 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125510021 12551002 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125510021 12551002 Acute kidney injury

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

no results found

Therapies reported

no results found