FDA Warns of Serious Side Effects in Dogs Treated with Librela

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FDA Warns of Serious Side Effects in Dogs Treated with Librela
FDALibrelaOsteoarthritis
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The FDA has issued a warning to veterinarians about potential adverse effects in dogs receiving Librela injections. The drug, used to treat osteoarthritis pain, has been linked to neurological problems, physical issues, and even death.

The Food and Drug Administration's ( FDA ) Center for Veterinary Medicine posted a letter to veterinarians on Monday warning about adverse effects reported in dogs following injections of Librela , a treatment aimed at providing pain relief for dogs with osteoarthritis.Dogster reports that there are an estimated 86.9 million dogs in the U.S.

The Morris Animal Foundation said about 14 million of those dogs live with osteoarthritis, also known as degenerative joint disease, which is a 'progressive disease of the joints fueled by chronic inflammation. The end result is chronic pain that can have far-ranging, negative health effects beyond an affected joint.' The FDA warned of several neurological and physical problems in dogs after receiving Librela injections.The letter comes after several reports revealed the adverse effects of the drug.The letter details several side effects, including ataxia—which causes lack of muscle control and coordination, seizures, paresis, recumbency, urinary incontinence, polyuria, and polydipsia.The most intense side effect is death, both naturally and by euthanasia.Users on a Facebook group, Librela: The REAL Truth in Testimony, often post about side effects they've noticed in their dogs who have been treated with the injection, some noticing spasms, neurological problems, and lack of appetite, among other effects. Librela, sponsored by Zoetis, is a monoclonal antibody drug that was approved by the FDA on May 5, 2023. Veterinarians administer the drug as a once-a-month injection, with the dosage determined by the dog's weight. It is available as a 5, 10, 15, 20, or 30 mg/ml solution injection

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