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
122970782 12297078 2 F 2008 20160914 20160422 20160921 EXP US-DSJP-DSU-2015-139625 DAIICHI 0.00 Y 0.00000 20160921 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
122970782 12297078 1 PS BENICAR OLMESARTAN MEDOXOMIL 1 UNK Y 21286 TABLET
122970782 12297078 2 SS BENICAR OLMESARTAN MEDOXOMIL 1 20 MG, UNK Y 21286 20 MG TABLET
122970782 12297078 3 SS BENICAR OLMESARTAN MEDOXOMIL 1 Oral 10 MG, QD Y 21286 10 MG TABLET QD
122970782 12297078 4 C VITAMINS /00067501/ VITAMINS 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122970782 12297078 1 Hypertension
122970782 12297078 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
122970782 12297078 HO
122970782 12297078 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122970782 12297078 Acute kidney injury
122970782 12297078 Adenocarcinoma of colon
122970782 12297078 Anxiety
122970782 12297078 Haemorrhoids
122970782 12297078 Hiatus hernia
122970782 12297078 Irritable bowel syndrome
122970782 12297078 Malabsorption
122970782 12297078 Osteoporosis

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
122970782 12297078 1 2006 0
122970782 12297078 2 2010 2012 0