The Safety Rates Drug Report

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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
124474172 12447417 2 F 20080826 20160628 20160608 20160705 EXP US-DSJP-DSU-2016-104916 DAIICHI 0.00 Y 0.00000 20160705 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
124474172 12447417 1 PS BENICAR OLMESARTAN MEDOXOMIL 1 Oral 40 MG, QD U 21286 40 MG TABLET QD
124474172 12447417 2 SS BENICAR OLMESARTAN MEDOXOMIL 1 20 MG, BID U 21286 20 MG TABLET BID
124474172 12447417 3 C ZELNORM TEGASEROD MALEATE 1 UNK 0
124474172 12447417 4 C BENTYL DICYCLOMINE HYDROCHLORIDE 1 Oral 10 MG, BID 0 10 MG CAPSULE BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124474172 12447417 1 Hypertension
124474172 12447417 3 Product used for unknown indication
124474172 12447417 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124474172 12447417 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124474172 12447417 Ascites
124474172 12447417 Colonic haematoma
124474172 12447417 Impaired gastric emptying
124474172 12447417 Irritable bowel syndrome
124474172 12447417 Malabsorption
124474172 12447417 Syncope

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
124474172 12447417 1 2008 2015 0