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
119370214 11937021 4 F 2011 20160920 20160121 20160926 EXP US-DSJP-DSU-2015-120153 DAIICHI 0.00 Y 0.00000 20160926 MD 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
119370214 11937021 1 PS BENICAR OLMESARTAN MEDOXOMIL 1 40 MG, QD Y 21286 40 MG TABLET QD
119370214 11937021 2 SS BENICAR OLMESARTAN MEDOXOMIL 1 Oral 20 MG, QD Y 21286 20 MG TABLET QD
119370214 11937021 3 SS BENICAR HCT HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 Oral 40/25MG, QD 1001 DF Y 0 1 DF FILM-COATED TABLET QD
119370214 11937021 4 SS BENICAR HCT HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 Oral 40/12.5MG, QD 1001 DF Y 0 1 DF FILM-COATED TABLET QD
119370214 11937021 5 SS BENICAR HCT HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 UNK 1001 DF Y 0 FILM-COATED TABLET
119370214 11937021 6 SS TRIBENZOR AMLODIPINE BESYLATEHYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 40/5/12.5MG, QD U 0 1 DF FILM-COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119370214 11937021 1 Hypertension
119370214 11937021 3 Hypertension
119370214 11937021 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
119370214 11937021 OT
119370214 11937021 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
119370214 11937021 Acute kidney injury
119370214 11937021 Adenoma benign
119370214 11937021 Bowel movement irregularity
119370214 11937021 Cholecystitis chronic
119370214 11937021 Cholesterosis
119370214 11937021 Depression
119370214 11937021 Diverticulum intestinal
119370214 11937021 Gallbladder polyp
119370214 11937021 Gastric ulcer
119370214 11937021 Gastroduodenitis
119370214 11937021 Gastrointestinal sounds abnormal
119370214 11937021 Gastrointestinal stromal tumour
119370214 11937021 Gastrooesophageal reflux disease
119370214 11937021 Hiatus hernia
119370214 11937021 Ileus
119370214 11937021 Intestinal metaplasia
119370214 11937021 Liver function test abnormal
119370214 11937021 Malabsorption
119370214 11937021 Pancytopenia
119370214 11937021 Reactive gastropathy
119370214 11937021 Renal disorder
119370214 11937021 Small intestinal obstruction
119370214 11937021 Ureteral disorder

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
119370214 11937021 1 2013 201310 0
119370214 11937021 2 201310 0
119370214 11937021 3 20101207 20130902 0
119370214 11937021 4 20101207 0
119370214 11937021 5 2006 0
119370214 11937021 6 20150407 0