FDA: Librela Tied to 3,600+ Dog Adverse Reactions, Deaths

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The FDA issued a warning regarding Librela, a dog arthritis medication, following more than 3,600 reports of serious adverse reactions, including deaths.

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Ataxia, seizures, partial paralysis, and urinary complications are among the reported side effects.

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Librela, approved by the FDA in May 2023, is a monthly treatment for canine osteoarthritis.

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Devastating results, including kidney failure and euthanasia, have been reported by pet owners following treatment with Librela.

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Manufacturer Zoetis defends the safety of Librela, saying that adverse effects occur very rarely, in a population of 21 million doses distributed worldwide.

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Veterinarians are encouraged to make careful diagnoses and discuss the risks with pet owners before prescribing.

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The FDA advises labeling on Librela and that it urgently reports any events to it.

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The FDA with the statistics showing that 14 million U.S. dogs are suffering from osteoarthritis asks pet owners to see veterinarians for less risky alternatives.

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