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
125403191 12540319 1 I 2014 20150827 20160708 20160708 EXP US-DSJP-DSU-2015-127157 DAIICHI 71.33 YR F Y 117.91000 KG 20160708 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
125403191 12540319 1 PS BENICAR HCT HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 Oral 40/25 MG, QD Y 21532 1 DF FILM-COATED TABLET QD
125403191 12540319 2 C XANAX ALPRAZOLAM 1 5 MG, TID 0 5 MG TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125403191 12540319 1 Hypertension
125403191 12540319 2 Anxiety

Outcome of event

Event ID CASEID OUTC COD
125403191 12540319 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125403191 12540319 Constipation
125403191 12540319 Depression
125403191 12540319 Diverticulitis
125403191 12540319 Duodenitis
125403191 12540319 Haemorrhoids
125403191 12540319 Malabsorption
125403191 12540319 Polyp

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
125403191 12540319 1 201111 201405 0
125403191 12540319 2 2014 0