17 PATIENT COUNSELING INFORMATION
Advise the patient to read the FDA-approved patient labeling (Patient Information and Instructions for Use).
Hypersensitivity Reactions
Advise patients that serious hypersensitivity reactions may occur, and to notify their healthcare providers if they develop generalized rash, urticaria, shortness of breath, facial swelling and eosinophilia [see Warnings and Precautions (5.1)].
Breastfeeding
Advise women not to breastfeed while they are on OXBRYTA therapy [see Use in Specific Populations (8.2)].
Dosage and Administration
To avoid a dosing error from using the wrong formulation of OXBRYTA, strongly advise patients and caregivers to visually inspect the tablets to verify the correct formulation each time the prescription is filled [see Dosage and Administration (2) and How Supplied/Storage and Handling (16)].
Advise patients to:
- Store OXBRYTA at 20°C to 30°C (68°F to 86°F).
- Continue taking OXBRYTA every day for as long as their physician tells them.
- Do not take St John's wort while taking OXBRYTA.
- Swallow OXBRYTA tablets whole. Do not cut, crush, or chew the tablets.
- Do not swallow whole, cut, crush, or chew OXBRYTA tablets for oral suspension. Disperse OXBRYTA tablets for oral suspension in room temperature clear drink (such as drinking water, clear soda, apple juice, clear electrolyte drinks, clear flavored drinks, or clear sports drinks) before administration. The amount of liquid needed to disperse the tablets for oral suspension will depend on the dose (number of tablets prescribed) [see Dosage and Administration (2.7)].
- Take OXBRYTA with or without food.
- If a dose is missed or not consumed entirely, resume dosing the following day [see Dosage and Administration (2.7)].
PATIENT INFORMATION | ||||
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OXBRYTA® (ox brye ta) (voxelotor) tablets | OXBRYTA® (ox brye ta) (voxelotor) tablets for oral suspension | |||
This Patient Information has been approved by the U.S. Food and Drug Administration. | Revised: 10/2022 | |||
What is OXBRYTA? OXBRYTA is a prescription medicine used for the treatment of sickle cell disease in adults and children 4 years of age and older. It is not known if OXBRYTA is safe and effective in children with sickle cell disease below 4 years of age. | ||||
Do not take OXBRYTA if you or your child have had an allergic reaction to voxelotor or any of the ingredients in OXBRYTA. See the end of this leaflet for a list of the ingredients in OXBRYTA. | ||||
Before taking OXBRYTA, tell your healthcare provider about all of your medical conditions, including if you or your child:
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How should I take OXBRYTA?
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What should I avoid while taking OXBRYTA? Do not take St. John's wort during treatment with OXBRYTA. | ||||
What are the possible side effects of OXBRYTA? OXBRYTA can cause serious side effects, including:
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The most common side effects of OXBRYTA include: | ||||
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The most common side effects of OXBRYTA in children ages 4 to less than 12 years of age include: | ||||
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These are not all the possible side effects of OXBRYTA. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects to Global Blood Therapeutics, Inc. at 1-833-428-4968 (1-833-GBT-4YOU). | ||||
How should I store OXBRYTA?
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General information about the safe and effective use of OXBRYTA. Medicines are sometimes prescribed for purposes other than those listed in a Patient Information leaflet. Do not use OXBRYTA for a condition for which it was not prescribed. Do not give OXBRYTA to other people, even if they have the same symptoms that you have. It may harm them. You can ask your healthcare provider or pharmacist for information about OXBRYTA that is written for health professionals. | ||||
What are the ingredients of OXBRYTA? Active Ingredient: voxelotor Inactive Ingredients: OXBRYTA tablets: colloidal silicon dioxide, croscarmellose sodium, magnesium stearate, microcrystalline cellulose, and sodium lauryl sulfate. The 500 mg tablet film coating contains: polyethylene glycol 3350, polyvinyl alcohol, talc, titanium dioxide, and yellow iron oxide. The 300 mg tablet film coating contains: black and red iron oxide, polyethylene glycol 3350, polyvinyl alcohol, talc, and titanium dioxide. OXBRYTA tablets for oral suspension: artificial grape flavor, colloidal silicon dioxide, croscarmellose sodium, iron oxide pigment, magnesium stearate, microcrystalline cellulose, and sucralose. Manufactured for: Global Blood Therapeutics, Inc. South San Francisco, CA 94080, USA. OXBRYTA® © 2022 Global Blood Therapeutics, Inc. All rights reserved. For more information, call 1-833-428-4968 (1-833-GBT-4YOU) or go to www.OXBRYTA.com. |