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Media Mentions, Articles, News & Press Releases

Media Mentions

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October 26, 2022  -  DVM360 Live!™
 

In this segment of dvm360 Live!™, Sue Ettinger, DVM, DACVIM (oncology), introduces crofelemer delayed-release tablets (Canalevia-CA1) and explains how it works to control chemotherapy-induced canine diarrhea.

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-A new standard of care for the treatment of chemotherapy-induced diarrhea in dogs

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June 19, 2022  -  NPR’s Dog Talk® (and Kitties Too!)

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“[I’m] so thankful that we have these new products so we can get the diarrhea to resolve more quickly and get the dogs back and the owners happier again sooner.” (49:20)

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-Dr. Sue Ettinger mentions Canalevia-CA1 on the June 19, 2022 episode #784 of NPR’s Dog Talk® (and Kitties Too!) podcast, hosted by Tracie Hotchner.

Articles

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September 2022  -  Veterinary Practice News

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Why treating CID is so complicated

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August 2022  -  PetVet Magazine

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Navigating the Side Effects of Chemotherapy in Dogs

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June 2022  -  Veterinary Practice News

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How 'Going Green' Impacts Veterinarians

News & Press Releases

2022

2021

Contact Us

 

1 (877) 787-3001

info@canalevia.com

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Location

 

Jaguar Animal Health

200 Pine Street, Suite 600

San Francisco, CA 94104

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Conditionally approved by FDA pending a full demonstration of effectiveness under application number 141-552.

CAUTION: Federal (USA) law restricts this drug to use by or on the order of a licensed veterinarian. It is a violation of Federal Law to use this product other than as directed in the labeling.

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IMPORTANT SAFETY INFORMATION

For oral use in dogs only. Not for use in humans. Keep Canalevia®-CA1 (crofelemer delayed-release tablets) in a secure location out of reach of children and other animals. Consult a physician in case of accidental ingestion by humans. Do not use in dogs that have a known hypersensitivity to crofelemer. Prior to using Canalevia-CA1, rule out infectious etiologies of diarrhea. Canalevia-CA1 is a conditionally approved drug indicated for the treatment of chemotherapy-induced diarrhea in dogs. The most common adverse reactions included decreased appetite, decreased activity, dehydration, abdominal pain, and vomiting.

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian. Use only as directed. It is a violation of Federal law to use this product other than as directed in the labeling. Conditionally approved by FDA pending a full demonstration of effectiveness under application number 141-552.

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