Dosage and Administration of Prednisone for MG

Your doctor will determine the appropriate prednisone dosage for your myasthenia gravis (MG), based on your specific needs and response to treatment. Treatment typically begins with a high dose, often 60-80mg daily, gradually tapered down over weeks or months. This high initial dose helps control symptoms quickly. The tapering schedule is individualized; a common approach might involve reducing the dose by 5-10mg every few days or weeks. Always follow your doctor’s prescribed schedule precisely. Don’t adjust your dosage without consulting them.

Monitoring Your Progress

Regular monitoring is key. Your physician will track your MG symptoms and adjust the prednisone dosage accordingly. Blood tests may be used to monitor your blood cell counts and liver function, given the potential side effects of prednisone. Be prepared to report any new or worsening symptoms, as well as any side effects, like weight gain, fluid retention, increased appetite, or mood changes. Open communication with your doctor is vital for successful management.

Alternative Administration

Prednisone is usually administered orally as a tablet. Your doctor may recommend alternative administration methods, like intravenous prednisone in cases of severe MG exacerbation. However, oral administration is generally preferred for long-term treatment. Always carefully follow instructions for taking the medication. For example, take it with food to minimise stomach upset.