Prescription medication · ACL Inhibitor / Cholesterol Absorption Inhibitor
bempedoic acid/ezetimibe
Also sold as Nexlizet. Nexlizet is used to lower LDL-C (bad cholesterol) in adults who have high cholesterol.
Data updated 2026-05-15
- 329
- FDA reports
- 7
- InteractionsFew interactions
- $13.05
- Brand price (NADAC)
What the data shows
bempedoic acid/ezetimibe (Nexlizet) is a prescription ACL Inhibitor / Cholesterol Absorption Inhibitor, with 329 FDA adverse-event reports on file, with 7 documented drug interactions.
Reporting volume reflects how widely a drug is used and studied, not how dangerous it is, a FAERS report documents a temporal association, never proof of cause.
bempedoic acid/ezetimibe (Nexlizet) is a prescription ACL Inhibitor / Cholesterol Absorption Inhibitor. Nexlizet is used to lower LDL-C (bad cholesterol) in adults who have high cholesterol.
Nexlizet is a combination medicine that helps lower cholesterol. It is used with diet and exercise to lower LDL-C (bad cholesterol) in adults.
Verify with FDA → · CMS NADAC pricing →
Drug Pricing (NADAC)
Brand Price
$13.05/unit
Generic Available
No
Pricing data from NADAC (CMS), effective December 18, 2024. Compare all drug costs →
What it does
Nexlizet is used to lower LDL-C (bad cholesterol) in adults who have high cholesterol.
Common side effects
Upper respiratory tract infection (like a cold), Muscle spasms, High uric acid levels in the blood
Key warnings
This medicine can raise uric acid levels in your blood, which can cause gout.
The sections below are summarized in plain English from bempedoic acid/ezetimibe's FDA-approved prescribing information. They describe what the official label says, and are not personal medical advice.
How It Works
Nexlizet contains two medicines that work in different ways to lower cholesterol. Bempedoic acid blocks an enzyme in your liver that makes cholesterol. Ezetimibe stops your body from absorbing cholesterol from food.
How to Take It
Take one Nexlizet tablet each day. You can take it with or without food. Swallow the tablet whole with a glass of water. If you miss a dose, take it as soon as you remember. But do not take two doses at the same time.
This is a plain-language summary of bempedoic acid/ezetimibe's FDA labeling, not individualized dosing advice. Ask a pharmacist or prescriber before changing how you take this medication.
Pregnancy & Breastfeeding
This medicine may harm your unborn baby. Do not take Nexlizet if you are pregnant or planning to become pregnant. Talk to your doctor about other ways to lower your cholesterol during pregnancy.
This is a plain-language summary of bempedoic acid/ezetimibe's FDA labeling, not individualized advice. Ask a pharmacist or prescriber about pregnancy or breastfeeding on this medication.
Missed Dose
If you miss a dose, take it as soon as you remember. Do not take two doses at the same time to make up for the missed dose.
This is a plain-language summary of bempedoic acid/ezetimibe's FDA labeling, not individualized advice. Ask a pharmacist or prescriber what to do about your specific missed dose.
Storage
Store Nexlizet at room temperature, between 68°F to 77°F (20°C to 25°C), in the original package, away from heat and humidity. Keep the desiccant in the bottle.
Side Effects (from patient reports)
Based on 329 FDA adverse event reports.
Most-reported reactions
Adverse reactions in FAERS for bempedoic acid/ezetimibe, by number of reports
- Muscle pain
Muscle pain
53 reports
- Joint pain
Joint pain
51 reports
- Pain in your arms or legs
Pain in your arms or legs
40 reports
- Muscle spasms
Muscle spasms
32 reports
- Tiredness
Tiredness
30 reports
- Back pain
Back pain
26 reports
- Headache
Headache
26 reports
- Diarrhea
Diarrhea
24 reports
- Pain
Pain
24 reports
- Rash
Rash
23 reports
What this shows Bars show how often each reaction was reported, not how likely it is to happen, a report records a temporal association, never proof that the drug caused it.
Serious Warnings
This medicine can raise uric acid levels in your blood, which can cause gout. Tell your doctor if you have symptoms of high uric acid, like joint pain or swelling. Nexlizet can also increase your risk of tendon rupture. Stop taking Nexlizet and call your doctor right away if you have tendon pain, swelling, or difficulty moving.
Known Drug Interactions
Clinically Important Drug Interactions with NEXLIZET Simvastatin Clinical Impact: Concomitant use of NEXLIZET with simvastatin causes an increase in simvastatin concentration and may increase the risk of simvastatin-related myopathy [see Clinical Pharmacology (12.3) ] . Intervention: Avoid concomitant use of NEXLIZET with simvastatin greater than 20 mg. Simvastatin: Avoid concomitant use of NEXLIZET with simvastatin greater than 20 mg.
Mechanism: Taking these together can cause simvastatin levels to rise in your body, which may lead to muscle pain or weakness.
What to do: Avoid taking more than 20 mg of simvastatin daily when using this medication.
Pravastatin Clinical Impact: Concomitant use of NEXLIZET with pravastatin causes an increase in pravastatin concentration and may increase the risk of pravastatin-related myopathy [see Clinical Pharmacology (12.3) ] . Intervention: Avoid concomitant use of NEXLIZET with pravastatin greater than 40 mg. ( 7 ) Pravastatin: Avoid concomitant use of NEXLIZET with pravastatin greater than 40 mg.
Mechanism: This medicine can raise the levels of pravastatin in your blood, which may lead to muscle pain or weakness.
What to do: Avoid taking more than 40 mg of pravastatin daily when using this medication.
Fibrates Clinical Impact: Both fenofibrate and ezetimibe (a component of NEXLIZET) may increase cholesterol excretion into the bile, leading to cholelithiasis. Coadministration of NEXLIZET with fibrates other than fenofibrate is not recommended [see Adverse Reactions (6.1) ] . Intervention: If cholelithiasis is suspected in a patient receiving NEXLIZET and fenofibrate, gallbladder studies are indicated and alternative lipid-lowering therapy should be considered.
Mechanism: Both of these medicines can increase the amount of cholesterol that moves into the bile, which may cause gallstones to form.
What to do: If you suspect you have gallstones, your doctor should perform tests and may consider a different treatment.
7 DRUG INTERACTIONS No specific pharmacokinetic drug interaction studies with NEXLIZET have been conducted. Table 4 lists drug interactions with NEXLIZET that have been identified in studies with bempedoic acid or ezetimibe. Clinically Important Drug Interactions with NEXLIZET Simvastatin Clinical Impact: Concomitant use of NEXLIZET with simvastatin causes an increase in simvastatin concentration and may increase the risk of simvastatin-related myopathy [see Clinical Pharmacology (12.3) ] .
Mechanism: This combination can cause simvastatin levels to build up in your body, which increases the risk of muscle damage.
What to do: Your doctor may need to adjust your dose or monitor you closely for muscle pain.
Table 4 lists drug interactions with NEXLIZET that have been identified in studies with bempedoic acid or ezetimibe. Cyclosporine Clinical Impact: Concomitant use of NEXLIZET and cyclosporine increases ezetimibe and cyclosporine concentrations. The degree of increase in ezetimibe exposure may be greater in patients with severe renal insufficiency [see Clinical Pharmacology (12.3) ] .
Mechanism: These medicines increase each other's levels in the body, and this effect can be even stronger if you have severe kidney issues.
What to do: Your doctor should monitor your medicine levels closely, especially if you have poor kidney function.
This is a plain-language summary of interactions documented in FDA labeling, not individualized advice. Ask a pharmacist or prescriber before combining medications.
Common Questions
What should I do if I experience muscle pain while taking Nexlizet?
Can I take Nexlizet with other cholesterol-lowering medications?
How often should I have my cholesterol levels checked while taking Nexlizet?
Can Nexlizet cause liver problems?
Is it safe to drink alcohol while taking Nexlizet?
What if I have kidney problems?
Can Nexlizet affect my blood sugar?
Are there any foods I should avoid while taking Nexlizet?
How long will I need to take Nexlizet?
What if I am taking other medications?
What are the common side effects of bempedoic acid/ezetimibe?
Does bempedoic acid/ezetimibe interact with other medications?
What drug class is bempedoic acid/ezetimibe?
Is bempedoic acid/ezetimibe safe during pregnancy?
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What the FDA Data Shows for bempedoic acid/ezetimibe
The FDA label for bempedoic acid/ezetimibe (sold under brand names such as Nexlizet) classifies it as a prescription-only medication in the ACL Inhibitor / Cholesterol Absorption Inhibitor class. Nexlizet is used to lower LDL-C (bad cholesterol) in adults who have high cholesterol. Official labeling lists 14 commonly reported side effects, including Upper respiratory tract infection (like a cold), Muscle spasms, High uric acid levels in the blood.
Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 329 voluntary reports. The database also lists 7 documented drug interactions derived from FDA labeling, with the top-flagged interaction rated moderate severity. NADAC pricing from CMS.
Report counts do not establish causation, a FAERS entry documents a temporal association, not proof that the drug produced the outcome. Widely prescribed medications naturally accumulate more reports than niche therapies, so raw totals must be interpreted alongside total exposure. Shortage status, recall history, and patent information further shape supply and switching decisions. This page summarizes public FDA data for educational purposes only and is not a substitute for professional medical advice, always consult a licensed healthcare provider before starting, stopping, or changing any medication.
Data Sources
Drug labeling: FDA Drug Labels (SPL/DailyMed). Adverse events: FDA Adverse Event Reporting System (FAERS). Pricing: CMS National Average Drug Acquisition Cost (NADAC).
FAERS reports are voluntary and do not establish causation. Drug interactions are derived from FDA labeling and clinical references. Always consult a healthcare professional before making medication decisions.
Last updated: January 15, 2026
Read our methodology - how this data is sourced, computed, and verified.
Data currency: FDA FAERS adverse-event reports through 2025, CMS NADAC acquisition-cost pricing effective December 2024, compiled and last refreshed May 2026. See our methodology for per-source dates and refresh cadence. Spot a figure that looks wrong? Report a correction.
All federal data sources used on this page
- FDA Orange Book - approved drug products with therapeutic equivalence. accessdata.fda.gov/cder/ob
- FDA DailyMed - NIH-hosted drug labeling for FDA-approved meds. dailymed.nlm.nih.gov
- FDA Adverse Event Reporting System (FAERS) - post-marketing safety surveillance. fda.gov/drugs/faers
- NLM RxNorm - standardized clinical drug nomenclature. nlm.nih.gov/research/umls/rxnorm
- CMS Medicare Part B Drug Average Sales Price Files - federal drug pricing data. cms.gov/medicare/part-b-drugs/asp
- FDA Drug Shortages Database - current and resolved drug shortage tracking. accessdata.fda.gov/drugshortages