Yes, tezepelumab (Tezspire) is FDA approved. The FDA granted approval for Tezspire on December 17, 2021, as an add-on maintenance treatment for severe asthma. This medication is specifically for patients whose asthma is not adequately controlled with their current medication regimen.
Tezepelumab is designed to be used in conjunction with other asthma medications to help control severe asthma. It is administered as a subcutaneous injection and is not intended for immediate relief of acute asthma attacks or bronchospasms. Patients should seek immediate medical attention if they experience worsening breathing problems or if their medications do not seem to be effective.
Common side effects of tezepelumab include:
Serious side effects that require immediate medical attention include signs of an allergic reaction, such as:
Patients experiencing any unusual symptoms should contact their doctor for medical advice. Side effects can be reported to the FDA at 1-800-FDA-1088.
Tezepelumab may interact with other medications, including prescription and over-the-counter drugs, vitamins, and herbal products. Patients should inform their doctor about all medications they are taking.
Tezepelumab (Tezspire) is an FDA-approved medication for the maintenance treatment of severe asthma in patients 12 years and older. Approved on December 17, 2021, it is administered as a subcutaneous injection every 4 weeks. While effective in controlling severe asthma, patients should be aware of potential side effects and interactions with other medications. Always consult a healthcare provider for personalized medical advice and treatment plans.
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