Teplizumab, marketed under the brand name Tzield, was approved by the FDA on November 17, 2022. This medication is used to delay the onset of stage 3 type 1 diabetes in individuals who are at least 8 years old and have stage 2 type 1 diabetes.
Usage: Teplizumab is administered as an intravenous infusion over approximately 30 minutes. The treatment involves daily infusions for 14 consecutive days. Prior to starting the therapy, your doctor will conduct tests to confirm the presence of stage 2 type 1 diabetes.
Side Effects: Patients should be aware of potential side effects, which can range from mild to severe. Common side effects include:
More serious side effects requiring immediate medical attention include:
Warnings:
Before Taking This Medicine: Before starting treatment with teplizumab, discuss with your doctor if you have:
Administration: Teplizumab is given as an infusion into a vein once daily for 14 days. It is important to follow all prescription label instructions and read all medication guides or instruction sheets. Your doctor may adjust, delay, or permanently discontinue your treatment based on side effects.
Dosing Information: The usual dose is based on body surface area and is administered by intravenous infusion once daily:
Precautions:
What to Avoid: Avoid receiving inactivated, mRNA, and "live" vaccines during treatment with teplizumab, as the vaccine may not work as effectively.
Drug Interactions: Teplizumab may interact with other medications, including prescription and over-the-counter medicines, vitamins, and herbal products. Inform your doctor about all the medicines you use to avoid harmful interactions.
Conclusion: Teplizumab (Tzield) is FDA approved for delaying the onset of stage 3 type 1 diabetes in individuals 8 years and older with stage 2 type 1 diabetes. Patients should be aware of potential side effects and interactions with other medications. Regular monitoring and communication with healthcare providers are essential for safe and effective treatment.
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