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
124536922 12453692 2 F 201305 20160517 20160609 20160720 PER US-DSJP-DSU-2016-112194 DAIICHI 46.44 YR F Y 122.00000 KG 20160718 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
124536922 12453692 1 PS BENICAR HCT HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 40/25 MG, UNK 21532 1 DF FILM-COATED TABLET
124536922 12453692 2 SS BENICAR OLMESARTAN MEDOXOMIL 1 UNK Y 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124536922 12453692 1 Hypertension
124536922 12453692 2 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124536922 12453692 Candida infection
124536922 12453692 Gastrooesophageal reflux disease
124536922 12453692 Hiatus hernia
124536922 12453692 Malabsorption
124536922 12453692 Perivascular dermatitis

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
124536922 12453692 1 201003 2014 0
124536922 12453692 2 201011 20140401 0