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Gasper’s experience with CREXONT is his own and may not reflect the experience of every patient. Most common side effects include nausea and anxiety. For some people, CREXONT may cause falling asleep during daily activities. Individual results will vary. Always speak with your doctor to determine if CREXONT may be right for you. Only a healthcare provider can assess your condition and guide you to the appropriate treatment options. INDICATION CREXONT® (carbidopa and levodopa) extended-release capsules is a prescription medication for the treatment of Parkinson’s disease, Parkinson’s disease caused by infection or inflammation of the brain, or Parkinson’s disease-like symptoms that may result from carbon monoxide or manganese poisoning in adults. IMPORTANT SAFETY INFORMATION Do not take CREXONT with antidepressant medications known as nonselective monoamine oxidase (MAO) inhibitors. Do not take CREXONT with other carbidopa-levodopa preparations without consulting your healthcare provider. CREXONT may cause falling asleep during activities of daily living, somnolence, or dizziness. Avoid activities that require alertness such as driving and operating machinery until you know how CREXONT affects you. The most common side effects that may occur with CREXONT are nausea and anxiety. It is important to avoid sudden discontinuation or rapid dose reduction of CREXONT. If you are discontinuing CREXONT, work with your healthcare provider to taper the dose over time to reduce the risk of fever or confusion. You may take CREXONT with or without food, but taking it with food may decrease or delay its effect. Consider taking the first dose of the day about 1 to 2 hours before eating. Swallow CREXONT whole. Do not chew, divide, or crush the capsules. Do not take CREXONT with alcohol. Tell your healthcare provider if you: Have any heart conditions, especially if you have had a heart attack or irregular heartbeats Experience hallucinations or abnormal thoughts and behaviors Have an inability to control urges to gamble, have increased sexual urges, or experience other intense urges Have thoughts of suicide or have attempted suicide Have abnormal involuntary movements that appear or get worse during treatment Have ever had a peptic ulcer or glaucoma Become or intend to become pregnant. Based on animal data, CREXONT may cause fetal harm Are breastfeeding during therapy To report SUSPECTED ADVERSE REACTIONS, contact Amneal Specialty, a division of Amneal Pharmaceuticals, LLC at 1-877-835-5472 or the FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. Please read the full Prescribing Information. For more information talk to your healthcare provider. PP ADV CREX US 0029 10/2026