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Telepractice

The Rise of Telehealth in the United States: The present and the future of dysphagia telerehabilitation

Cagla Kantarcigil, MS, SLP - August 24, 2016
0

Dysphagia management via telepractice: What’s the evidence and where to from here?

Elizabeth Ward - December 9, 2015
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Dysphagia education: Rewind on 2016

Dysphagia Cafe - December 31, 2016
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ENRICHMENT WEBINARS

  • Cardiac ICU Dysphagia Cough Webinar Continuing Education Leveraging the Data to Optimize Swallow and Cough Care in Cardiothoracic Intensive Care Units $15.00
  • Competency in Dysphagia webinar by Jordan Hazelwood from Appalachian State University Enhancing Competency in Dysphagia Management $15.00
  • Comfort Care and Dysphagia Webinar by Paula Leslie How Do We Define Comfort PO? $15.00

Scroll for Important Safety Information

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.

TIMS MEDICAL
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