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Zycortal Injectable Suspension for Dogs is a prescription medication specifically formulated for the treatment of primary hypoadrenocorticism (Addison's disease) in dogs. Addison’s disease is a serious condition caused by insufficient hormone production from the adrenal glands, resulting in symptoms such as lethargy, vomiting, weight loss, and weakness. Zycortal contains desoxycorticosterone pivalate (DOCP), a long-acting mineralocorticoid that helps regulate sodium and potassium balance to maintain healthy electrolyte levels and blood pressure.
Zycortal delivers desoxycorticosterone pivalate, a synthetic mineralocorticoid that mimics the function of natural hormones produced by healthy adrenal glands. It helps restore balance to sodium and potassium levels in the bloodstream and supports blood pressure regulation. By replacing the missing hormone, Zycortal helps control the clinical signs of Addison’s disease and prevents potentially life-threatening adrenal crises.
Zycortal is indicated for use in dogs diagnosed with primary adrenocortical insufficiency (Addison’s disease). It is used in combination with glucocorticoid therapy to restore and maintain hormonal balance, alleviate clinical signs, and support long-term health and stability.
Do not use Zycortal in animals with known hypersensitivity to desoxycorticosterone. Use caution in dogs with pre-existing heart disease, kidney disease, or fluid retention issues. Always follow your veterinarian's dosing recommendations. Periodic blood tests may be required to monitor electrolyte levels.
Ingredient | Function | Amount |
---|---|---|
Desoxycorticosterone Pivalate | Mineralocorticoid hormone replacement | 25 mg/mL |
Desoxycorticosterone pivalate is the sole active ingredient in Zycortal. It acts as a synthetic mineralocorticoid used to replace the hormone normally produced by the adrenal glands, helping to regulate sodium and potassium levels and maintain healthy blood pressure in dogs with Addison's disease.
Download the Zycortal Suspension Package Insert (PDF)
Important Usage Instructions: Shake the vial thoroughly before each use to ensure proper suspension. Zycortal Suspension is a mineralocorticoid replacement therapy and does not replace glucocorticoids. Dogs with both glucocorticoid and mineralocorticoid deficiency must also receive an appropriate glucocorticoid, such as prednisone.
Long-Term Administration: Zycortal is intended for long-term use with dosage and injection intervals tailored to each dog based on clinical signs and sodium/potassium (Na⁺/K⁺) balance.
Administer an initial dose of 2.2 mg/kg body weight via subcutaneous injection.
At approximately 10 days after the first injection (the time of peak concentration), assess the Na⁺/K⁺ ratio and the dog's clinical status. If symptoms persist or worsen, adjust the glucocorticoid dosage or investigate alternative causes.
Reevaluate the dog and repeat the Na⁺/K⁺ test around Day 25. Follow the guidelines below to adjust the Zycortal dose:
Table 1: Second Dose Adjustment Based on Day 10 Na⁺/K⁺ Ratio | ||
---|---|---|
Day 10 Na⁺/K⁺ Ratio | Action on Day 10 | Day 25 Dose Recommendation |
≥ 34 | Do not give Dose 2 on Day 10 | Reduce dose to 2.0 mg/kg |
32 to < 34 | Do not give Dose 2 on Day 10 | Reduce dose to 2.1 mg/kg |
27 to 32 | Do not give Dose 2 on Day 10 | Maintain dose at 2.2 mg/kg |
24 to < 27 | Do not give Dose 2 on Day 10 | Increase dose to 2.3 mg/kg |
< 24 | Do not give Dose 2 on Day 10 | Increase dose to 2.4 mg/kg |
If the dog is stable with a Na⁺/K⁺ ratio > 32 at Day 25, consider delaying the next injection. Monitor electrolyte levels every 3–7 days. When the Na⁺/K⁺ ratio drops below 32, administer 2.2 mg/kg of Zycortal Suspension.
Adjust future doses based on clinical response and electrolyte levels:
Prior to stressful events (e.g., travel, surgery), consider a temporary increase in glucocorticoid dosage.
Do not use Zycortal in dogs with known hypersensitivity to desoxycorticosterone pivalate.
Keep out of reach of children and animals.
Store between 15°C and 30°C (59°F–86°F). Do not freeze. Use within 120 days after first puncture of the vial.