IMPORTANT SAFETY INFORMATION
CONTRAINDICATIONS
QULIPTA is contraindicated in patients with a history of hypersensitivity to atogepant or any of the components of QULIPTA.
WARNINGS AND PRECAUTIONS
Cases, including anaphylaxis, dyspnea, rash, pruritus, urticaria, and facial edema, have been reported with use of QULIPTA. Hypersensitivity reactions can occur days after administration. If a hypersensitivity reaction occurs, discontinue QULIPTA and institute appropriate therapy.
ADVERSE REACTIONS
The most common adverse reactions (at least 4% and greater than placebo) are nausea, constipation, and fatigue/somnolence.
Dosage form and strengths: QULIPTA is available in 10 mg, 30 mg, and 60 mg tablets.
INDICATION
QULIPTA® (atogepant) is indicated for the preventive treatment of migraine in adults.
Please see full Prescribing Information.
*Managed Markets Insight & Technology, LLC, a trademark of MMIT. Data as of August 2023 and subject to change.
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US-QLP-230521 11/23