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
124483412 12448341 2 F 200512 20160726 20160608 20160802 EXP US-DSJP-DSU-2016-108220 DAIICHI 0.00 Y 0.00000 20160802 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
124483412 12448341 1 PS BENICAR OLMESARTAN MEDOXOMIL 1 Oral 40 MG, QD Y 21286 40 MG TABLET QD
124483412 12448341 2 SS BENICAR OLMESARTAN MEDOXOMIL 1 UNK Y 21286 TABLET
124483412 12448341 3 SS BENICAR HCT HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 40/25MG, UNK U 0 1 DF FILM-COATED TABLET
124483412 12448341 4 C NSAID'S UNSPECIFIED INGREDIENT 1 UNK 0
124483412 12448341 5 C MULTIVITAMINS VITAMINS 1 Oral UNK 0 TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124483412 12448341 1 Hypertension
124483412 12448341 3 Hypertension
124483412 12448341 4 Arthritis
124483412 12448341 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124483412 12448341 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124483412 12448341 Coeliac disease
124483412 12448341 Dysphagia
124483412 12448341 Gastrooesophageal reflux disease
124483412 12448341 Heart rate irregular
124483412 12448341 Hiatus hernia
124483412 12448341 Malabsorption
124483412 12448341 Renal failure

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
124483412 12448341 1 200409 20140515 0
124483412 12448341 2 2008 0
124483412 12448341 3 200409 200906 0