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
84984794 8498479 4 F 20160715 20120406 20160727 EXP US-ASTRAZENECA-2012SE21655 ASTRAZENECA 67.00 YR M Y 96.60000 KG 20160727 US US

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
84984794 8498479 1 PS CRESTOR ROSUVASTATIN CALCIUM 1 Oral U U 21366 20 MG TABLET QD
84984794 8498479 2 SS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral U U 0 40 MG CAPSULE QD
84984794 8498479 3 SS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral 40.0MG UNKNOWN U U 0 40 MG CAPSULE
84984794 8498479 4 SS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral GENERIC UNKNOWN U U 0
84984794 8498479 5 SS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral U U 0
84984794 8498479 6 C RANEXA RANOLAZINE 1 0
84984794 8498479 7 C ASPIRIN. ASPIRIN 1 0
84984794 8498479 8 C COREG CARVEDILOL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
84984794 8498479 1 Cardiac disorder
84984794 8498479 2 Gastrooesophageal reflux disease
84984794 8498479 3 Gastrooesophageal reflux disease
84984794 8498479 4 Gastrooesophageal reflux disease
84984794 8498479 5 Gastrooesophageal reflux disease

Outcome of event

Event ID CASEID OUTC COD
84984794 8498479 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
84984794 8498479 Abdominal discomfort
84984794 8498479 Anxiety
84984794 8498479 Dementia
84984794 8498479 Drug dose omission
84984794 8498479 Feeling abnormal
84984794 8498479 Gastric disorder
84984794 8498479 Hypoacusis
84984794 8498479 Intentional product misuse
84984794 8498479 Malaise
84984794 8498479 Memory impairment

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

no results found

Therapies reported

no results found