Tezspire has been around since it was first approved by the FDA in December of 2021.
The adverse reactions to Tezspire include trouble breathing, severe dizziness, rash, itching and swelling of the face, tongue and throat.
If you notice any of these adverse and serious reactions to Tezpire you should seek medical attention right away.
The generic name for Tezspire is Tezepelumab-ekko.
Tezspire is not available in a biosimilar form. (Biosimilars are like generic drugs.
But unlike generics, which are made for non-biologic drugs, biosimilars are made for biologic drugs.)
Instead, tezepelumab-ekko comes only as the brand-name drug Tezspire.
The drug Tezpire is a treatment for severe asthma that proactively reduces inflammation, which means you could experience: Fewer asthma attacks.
Better breathing and improved lung function and improved asthma symptom control.
The cost for Tezspire subcutaneous solution (ekko 210 mg/1.91 mL) is around $4,061.00 for a supply of 1.91 milliliters, depending on the pharmacy you visit.
The Patient Assistance Program provides TEZSPIRE to qualified patients at no cost.
Eligible patients must meet certain requirements including being uninsured or underinsured on Medicare Part B without supplemental insurance or on Medicare Advantage with an affordability gap.
Do not take TEZSPIRE if you are allergic to tezepelumab or any of the ingredients in TEZSPIRE.
The most common side effects of TEZSPIRE include: Sore throat (pharyngitis) Joint pain (arthralgia)
Other side effects of Tezpire include.
Back pain.
Body aches or pain.
Cough.
Difficulty in moving.
Dryness or soreness of the throat.
Fever.
Muscle pain or stiffness.
Redness, pain, or itching at the injection site.
Although Tezspire begins working shortly after your first dose, it's likely to take several weeks or even months before you notice your symptoms begin to ease.
However some people receiving Tezspire in studies saw a reduction in their asthma symptoms as soon as 2 weeks after the first dose.
The recommended dosage of TEZSPIRE is 210 mg administered subcutaneously once every 4 weeks.
If a dose is missed, administer the dose as soon as possible.
Thereafter, the patient can continue (resume) dosing on the usual day of administration.
If the next dose is already due, then administer as planned.