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
125187072 12518707 2 F 2011 20160913 20160630 20160920 EXP US-DSJP-DSU-2015-120682 DAIICHI 0.00 Y 0.00000 20160920 LW 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
125187072 12518707 1 PS BENICAR OLMESARTAN MEDOXOMIL 1 Oral 20 MG, QD U 21286 20 MG TABLET QD
125187072 12518707 2 SS BENICAR HCT HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 Oral 40/25 MG, QD U 0 1 DF FILM-COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125187072 12518707 1 Product used for unknown indication
125187072 12518707 2 Hypertension

Outcome of event

Event ID CASEID OUTC COD
125187072 12518707 OT
125187072 12518707 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125187072 12518707 Acute kidney injury
125187072 12518707 Appendicitis
125187072 12518707 Chronic hepatitis C
125187072 12518707 Constipation
125187072 12518707 Dizziness
125187072 12518707 Gastrointestinal haemorrhage
125187072 12518707 Gastrooesophageal reflux disease
125187072 12518707 Haemorrhoids
125187072 12518707 Hypotension
125187072 12518707 Iron deficiency anaemia
125187072 12518707 Large intestine polyp
125187072 12518707 Malabsorption

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
125187072 12518707 2 2006 2014 0