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
125859331 12585933 1 I 20160627 20160628 20160725 20160725 PER US-ASTRAZENECA-2016SE71359 ASTRAZENECA 65.55 YR M Y 81.60000 KG 20160725 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
125859331 12585933 1 PS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 MCG 1 PUFF TWICE A DAY 21929
125859331 12585933 2 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 MCG 2 PUFF TWICE A DAY 21929
125859331 12585933 3 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 MCG 1 PUFF TWICE A DAY 21929
125859331 12585933 4 SS METOPROLOL SUCCINATE. METOPROLOL SUCCINATE 1 Oral 0 25 MG MODIFIED-RELEASE TABLET QD
125859331 12585933 5 C PLAVIX CLOPIDOGREL BISULFATE 1 Oral 0 75 MG QD
125859331 12585933 6 C LIPITOR ATORVASTATIN CALCIUM 1 Oral 0 40 MG QD
125859331 12585933 7 C ZETIA EZETIMIBE 1 Oral 0 10 MG QD
125859331 12585933 8 C ASPIRIN. ASPIRIN 1 Oral 0 81 MG QD
125859331 12585933 9 C FLOMAX TAMSULOSIN HYDROCHLORIDE 1 Oral 0 .4 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125859331 12585933 1 Chronic obstructive pulmonary disease
125859331 12585933 2 Chronic obstructive pulmonary disease
125859331 12585933 3 Chronic obstructive pulmonary disease
125859331 12585933 4 Coronary artery disease
125859331 12585933 5 Coronary artery disease
125859331 12585933 6 Blood cholesterol abnormal
125859331 12585933 7 Blood cholesterol abnormal
125859331 12585933 8 Coronary artery disease
125859331 12585933 9 Benign prostatic hyperplasia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125859331 12585933 Heart rate increased
125859331 12585933 Hypertension
125859331 12585933 Intentional product misuse
125859331 12585933 Off label use
125859331 12585933 Rash

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
125859331 12585933 1 20160615 0