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
124535232 12453523 2 F 20160115 20160609 20160720 EXP US-DSJP-DSU-2015-133590 DAIICHI 0.00 F Y 171.43000 KG 20160720 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
124535232 12453523 1 PS BENICAR HCT HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 20/12.5 MG, UNK Y 21532 20 MG FILM-COATED TABLET
124535232 12453523 2 SS BENICAR OLMESARTAN MEDOXOMIL 1 Oral 10 MG, QD U 0 10 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124535232 12453523 1 Hypertension
124535232 12453523 2 Hypertension

Outcome of event

Event ID CASEID OUTC COD
124535232 12453523 HO
124535232 12453523 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124535232 12453523 Acute kidney injury
124535232 12453523 Cystitis
124535232 12453523 Drug administration error
124535232 12453523 Dysuria
124535232 12453523 Gallbladder disorder
124535232 12453523 Hiatus hernia
124535232 12453523 Malabsorption
124535232 12453523 Nephrolithiasis
124535232 12453523 Oesophagitis

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
124535232 12453523 1 201112 2014 0