The Safety Rates Drug Report

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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
117928034 11792803 4 F 200606 20160902 20151202 20160910 EXP US-DSJP-DSU-2015-125762 DAIICHI 0.00 Y 0.00000 20160909 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
117928034 11792803 1 PS BENICAR HCT HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 40/25 MG, UNK N 21532 1 DF FILM-COATED TABLET
117928034 11792803 2 SS BENICAR OLMESARTAN MEDOXOMIL 1 40 MG, UNK U 0 40 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117928034 11792803 1 Hypertension
117928034 11792803 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
117928034 11792803 HO
117928034 11792803 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
117928034 11792803 Acquired oesophageal web
117928034 11792803 Cholelithiasis
117928034 11792803 Crohn's disease
117928034 11792803 Diabetic gastroparesis
117928034 11792803 Diverticulum
117928034 11792803 Gastrointestinal bacterial overgrowth
117928034 11792803 Gastrooesophageal reflux disease
117928034 11792803 Haemorrhoids
117928034 11792803 Hiatus hernia
117928034 11792803 Hospitalisation
117928034 11792803 Intestinal obstruction
117928034 11792803 Large intestine polyp
117928034 11792803 Malabsorption
117928034 11792803 Pancreatitis

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
117928034 11792803 1 2004 2005 0