Dizziness While Taking Zetia (Ezetimibe)
If you experience dizziness while taking Zetia, contact your healthcare provider immediately, as this is a recognized adverse effect that may require medication adjustment or discontinuation. 1
Understanding Dizziness as a Side Effect of Zetia
- Dizziness is listed as a known adverse effect in the FDA-approved prescribing information for ezetimibe (Zetia), occurring in post-marketing surveillance reports 1
- The FDA label specifically instructs patients to "stop using ezetimibe tablets and get medical help right away" if experiencing "fainting or feeling dizzy" as part of a serious allergic reaction 1
- Dizziness from ezetimibe appears to be relatively uncommon, as it was not among the most frequent adverse reactions (≥2%) reported in controlled clinical trials 1
Immediate Actions to Take
Contact your healthcare provider promptly to report the dizziness, especially if it is persistent, severe, or accompanied by other symptoms. 1
- Watch for signs of a serious allergic reaction that requires immediate medical attention, including: swelling of face/tongue/throat, difficulty breathing or swallowing, very fast heartbeat, severe skin rash, or flu-like symptoms 1
- Document when the dizziness occurs (timing relative to dose, activities that trigger it, duration, and severity) to help your provider assess the situation 2
- Check if you are taking other medications that could contribute to dizziness, as drug interactions may amplify this effect 1
Medication Review Considerations
- Your healthcare provider should review all medications you are taking, as ezetimibe can interact with cyclosporine, fibrates, and bile acid sequestrants, potentially affecting drug levels and side effects 1
- If you are taking ezetimibe with a statin, the combination may increase the risk of adverse effects compared to either medication alone 1
- Ezetimibe reaches peak concentrations 1-2 hours after administration and has a terminal half-life of approximately 22 hours, meaning it accumulates with repeated daily dosing 3
Clinical Decision Algorithm
Your healthcare provider will likely follow this approach:
Assess severity and pattern: Determine if dizziness represents true vertigo, presyncope, disequilibrium, or vague lightheadedness, as each has different implications 2
Rule out serious causes: Evaluate for signs of allergic reaction, cardiovascular issues, or other serious conditions that may coincidentally present with dizziness 1
Consider medication adjustment: Options include:
Monitor for resolution: If ezetimibe is discontinued, dizziness should improve within several days given the drug's elimination half-life of approximately 22 hours 3
Alternative Treatment Options
- If ezetimibe must be discontinued due to intolerable dizziness, your provider may consider other non-statin lipid-lowering options such as bempedoic acid, PCSK9 inhibitors (inclisiran, evolocumab, alirocumab), or bile acid sequestrants 4
- The choice of alternative therapy depends on your specific lipid profile, cardiovascular risk, and other medical conditions 4
Important Safety Considerations
- Do not stop taking ezetimibe without consulting your healthcare provider, as abrupt discontinuation of cholesterol-lowering therapy may affect your cardiovascular risk management 1
- Ezetimibe has an overall favorable safety profile with few serious adverse effects reported in clinical trials, but individual responses vary 5, 6
- If dizziness is accompanied by unexplained muscle pain, tenderness, weakness, or unusual fatigue, report this immediately as it may indicate myopathy, a rare but serious adverse effect 1
When to Seek Immediate Medical Attention
Go to the emergency department or call emergency services if you experience: 1
- Severe dizziness with loss of consciousness or near-fainting
- Dizziness accompanied by chest pain, shortness of breath, or irregular heartbeat
- Signs of allergic reaction (facial swelling, difficulty breathing, severe rash)
- Sudden onset of severe headache, vision changes, or difficulty speaking