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International

InternationalEric Blicker, MA CCC-SLP.D BCS-SDecember 21, 2021
InternationalRehabilitationGabriela Constantinescu, PhD, R.SLP, S-LP(C)October 4, 2021
InternationalEd Bice, M.Ed., CCC-SLPJuly 26, 2021
InternationalRehabilitationGabriela Constantinescu, PhD, R.SLP, S-LP(C)June 14, 2021
InternationalRehabilitationTreatmentLeticia FreixoFebruary 16, 2021
InternationalPediatricEna Heimdahl, MAApril 28, 2019
AnatomyAssessmentEvidence Based PracticeInstrumental AssessmentInternationalAnna Miles, PhDNovember 29, 2016
AssessmentInstrumental AssessmentInternationalCatriona Steele, Ph.D., CCC-SLP, BCS-SJuly 20, 2016
InternationalPediatricEna Heimdahl, MAApril 5, 2016
InternationalPediatricEna Heimdahl, MAMarch 30, 2016
Continuing EducationInternationalRinki Varindani Desai, M.S.CCC-SLPMarch 20, 2016
AssessmentInternationalTelepracticeTreatmentElizabeth WardDecember 9, 2015
AssessmentInstrumental AssessmentInternationalRehabilitationTreatmentEmilia Michou Ph.D., PGDip, CertMRCSLTJanuary 8, 2015
Art & ScienceInternationalLuis Riquelme, PhD, CCC-SLP, BCS-SNovember 15, 2014
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INDICATIONS AND USAGE:

VARIBAR ® THIN HONEY (barium sulfate) oral suspension, VARIBAR ® NECTAR (barium sulfate) oral suspension, and VARIBAR ® THIN LIQUID (barium sulfate) for oral suspension, are indicated for use in modified barium swallow examinations to evaluate the oral and pharyngeal function and morphology in adult and pediatric patients. VARIBAR ® HONEY (barium sulfate) oral suspension and VARIBAR ® PUDDING (barium sulfate) oral paste are indicated for use in modified barium swallow examinations to evaluate the oral and pharyngeal function and morphology in adult and pediatric patients 6 months of age and older.

IMPORTANT SAFETY INFORMATION:
For Oral Administration. This product should not be used in patients with known or suspected perforation of the GI tract, known obstruction of the GI tract, high risk of aspiration, or hypersensitivity to barium sulfate products. Rarely, severe allergic reactions of anaphylactoid nature have been reported following administration of barium sulfate contrast agents. Aspiration may occur during the modified barium swallow examination, monitor the patient for aspiration.

Please consult full Prescribing Information for VARIBAR products by clicking HERE.

You are encouraged to report negative side effects of prescription drugs to the FDA.
Visit FDA or call 1-800-FDA-1088.

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