The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
7489113 7830875 F 7489113-8 20101201 20110428 20110518 PER US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2011-BP-03307BP B.I. PHARMACEUTICALS,INC./RIDGEFIELD 69 YR F Y 20110518 CN UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
7489113 1016532709 C DIOVAN 1 ORAL 80 MG
7489113 1016532710 C DILTIAZEM 1 ORAL 120 MG
7489113 1016532713 C VITAMIN E 1
7489113 1016532711 C ALENDRONATE SODIUM 1 ORAL 10 MG
7489113 1016532708 SS PRADAXA 1 NOTREPORTED 022512
7489113 1016532712 C VITAMIN C 2
7489113 1016532714 C CALCIUM CARBONATE 1
7489113 1016532715 C GLUCOSAMINE 2
7489113 1016532707 PS PRADAXA 1 ORAL 300 MG NOTREPORTED 022512

Indications of drugs used

Event ID DRUG SEQ INDI PT
7489113 1016532709 BLOOD PRESSURE
7489113 1016532710 CARDIAC DISORDER
7489113 1016532713 SUPPLEMENTATION THERAPY
7489113 1016532711 OSTEOPOROSIS
7489113 1016532708 ANTICOAGULANT THERAPY
7489113 1016532712 SUPPLEMENTATION THERAPY
7489113 1016532714 SUPPLEMENTATION THERAPY
7489113 1016532715 ARTHROPATHY
7489113 1016532707 ATRIAL FIBRILLATION

Outcome of event

no results found

Reactions reported

Event ID PT
7489113 ABNORMAL FAECES

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
7489113 1016532709 20101215
7489113 1016532710 20101215
7489113 1016532707 20101215