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
124486902 12448690 2 F 2014 20160701 20160608 20160708 EXP US-DSJP-DSU-2016-112693 DAIICHI 0.00 Y 0.00000 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
124486902 12448690 1 PS BENICAR OLMESARTAN MEDOXOMIL 1 UNK U 21286 TABLET
124486902 12448690 2 SS BENICAR OLMESARTAN MEDOXOMIL 1 Oral 20 MG, QD U 21286 20 MG TABLET QD
124486902 12448690 3 SS BENICAR OLMESARTAN MEDOXOMIL 1 Oral 5 MG 2 TABLETS, QD U 21286 10 MG TABLET QD
124486902 12448690 4 SS BENICAR OLMESARTAN MEDOXOMIL 1 UNK U 21286 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124486902 12448690 1 Hypertension

Outcome of event

Event ID CASEID OUTC COD
124486902 12448690 OT
124486902 12448690 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124486902 12448690 Anxiety
124486902 12448690 Depression
124486902 12448690 Diverticulum intestinal
124486902 12448690 Drug prescribing error
124486902 12448690 Gastrooesophageal reflux disease
124486902 12448690 Haematuria
124486902 12448690 Hypertension
124486902 12448690 Intestinal atresia
124486902 12448690 Large intestinal stenosis
124486902 12448690 Malabsorption
124486902 12448690 Palpitations

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
124486902 12448690 1 20100101 0
124486902 12448690 2 2013 201510 0