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Media Mentions, Articles, News & Press Releases

Media Mentions

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

“[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)

-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

Why treating CID is so complicated

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August 2022  -  PetVet Magazine

Navigating the Side Effects of Chemotherapy in Dogs

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June 2022  -  Veterinary Practice News

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.

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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