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
125448361 12544836 1 I 20100423 20160108 20160711 20160711 EXP US-DSJP-DSU-2016-101679 DAIICHI 50.57 YR F Y 88.44000 KG 20160711 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
125448361 12544836 1 PS BENICAR HCT HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 Oral 20/12.5 MG DAILY Y 21532 FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125448361 12544836 1 Hypertension

Outcome of event

Event ID CASEID OUTC COD
125448361 12544836 OT
125448361 12544836 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125448361 12544836 Acute kidney injury
125448361 12544836 Anxiety
125448361 12544836 Constipation
125448361 12544836 Dizziness
125448361 12544836 Gastrooesophageal reflux disease
125448361 12544836 Haemorrhoids
125448361 12544836 Hydronephrosis
125448361 12544836 Hypotension
125448361 12544836 Large intestine polyp
125448361 12544836 Malabsorption
125448361 12544836 Renal cyst

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
125448361 12544836 1 20060317 2011 0