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
125378531 12537853 1 I 2010 20150629 20160707 20160707 EXP US-DSJP-DSU-2015-120677 DAIICHI 0.00 F Y 83.90000 KG 20160707 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
125378531 12537853 1 PS BENICAR HCT HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 UNK N 21532 FILM-COATED TABLET
125378531 12537853 2 SS BENICAR HCT HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 40/25 MG, UNK N 21532 FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125378531 12537853 1 Hypertension

Outcome of event

Event ID CASEID OUTC COD
125378531 12537853 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125378531 12537853 Anxiety
125378531 12537853 Depression
125378531 12537853 Diverticulum
125378531 12537853 Gastritis
125378531 12537853 Haemorrhoids
125378531 12537853 Inflammation
125378531 12537853 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
125378531 12537853 1 2005 0
125378531 12537853 2 2007 2010 0