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
125378251 12537825 1 I 2013 20150605 20160707 20160707 EXP US-DSJP-DSU-2015-117860 DAIICHI 0.00 M Y 136.50000 KG 20160707 PH 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
125378251 12537825 1 PS BENICAR HCT HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 Oral 40/25 MG, QD 21532 FILM-COATED TABLET QD
125378251 12537825 2 C BYSTOLIC NEBIVOLOL HYDROCHLORIDE 1 20 MG, UNK 0 20 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125378251 12537825 1 Hypertension
125378251 12537825 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125378251 12537825 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125378251 12537825 Abnormal faeces
125378251 12537825 Acute kidney injury
125378251 12537825 Constipation
125378251 12537825 Dyspepsia
125378251 12537825 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
125378251 12537825 1 2006 2014 0
125378251 12537825 2 2012 0