VASCEPA is available at a lower out-of-pocket cost than generic icosapent ethyl for most patients1*

Branded VASCEPA is covered by major national PBMs and health plans:

Vascepa bottle and capsule

Branded VASCEPA is covered by major national PBMs and health plans:

  • With a generic copay
  • With no prior authorizations or other restrictions
  • For ~40 million lives in the Commercial business segment

See if your patients have unrestricted access to VASCEPA

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VASCEPA is the exclusive formulary product for many commercial and Medicare Part D patients

  • VASCEPA is covered without restrictions for >90% of Medicare Part D patients
  • Approximately 60% of Medicare Part D patients have no coverage for generic icosapent ethyl

A range of access resources

Formulary Status for Select Plans
Formulary Status for Select Plans
State DAW Requirements
State DAW Requirements
ICD-10 Coding Flashcard
ICD-10 Coding Flashcard
Pharm Resource -DAW Codes
Pharm Resource -DAW Codes
PA Letter - General
PA Letter - General
PA Letter - Texas
PA Letter - Texas

Questions about prior authorizations?

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IMPORTANT SAFETY INFORMATION

VASCEPA is contraindicated in patients with known hypersensitivity (e.g., anaphylactic reaction) to VASCEPA or any of its components

VASCEPA was associated with an increased risk (3% vs 2%) of atrial fibrillation or atrial flutter requiring hospitalization in a double-blind, placebo-controlled trial. The incidence of atrial fibrillation was greater in patients with a previous history of atrial fibrillation or atrial flutter

It is not known whether patients with allergies to fish and/or shellfish are at an increased risk of an allergic reaction to VASCEPA. Patients with such allergies should discontinue VASCEPA if any reactions occur

INDICATIONS AND LIMITATIONS OF USE

VASCEPA® (icosapent ethyl) is indicated as an adjunct to maximally tolerated statin therapy to reduce the risk of myocardial infarction, stroke, coronary revascularization and unstable angina requiring hospitalization in adult patients with elevated triglyceride (TG) levels (≥150 mg/dL) and established cardiovascular disease or diabetes mellitus and 2 or more additional risk factors for cardiovascular disease

VASCEPA is indicated as an adjunct to diet to reduce TG levels in adult patients with severe (≥500 mg/dL) hypertriglyceridemia

The effect of VASCEPA on the risk for pancreatitis in patients with severe hypertriglyceridemia has not been determined.

VASCEPA was associated with an increased risk (12% vs 10%) of bleeding in a double-blind, placebo-controlled trial. The incidence of bleeding was greater in patients receiving concomitant antithrombotic medications, such as aspirin, clopidogrel or warfarin

Common adverse reactions in the cardiovascular outcomes trial (incidence ≥3% and ≥1% more frequent than placebo): musculoskeletal pain (4% vs 3%), peripheral edema (7% vs 5%), constipation (5% vs 4%), gout (4% vs 3%) and atrial fibrillation (5% vs 4%)

Common adverse reactions in the hypertriglyceridemia trials (incidence ≥1% more frequent than placebo): arthralgia (2% vs 1%) and oropharyngeal pain (1% vs 0.3%)

Adverse Events, Product Complaints, or Special Situations may be reported by contacting AmarinConnect at 1-855-VASCEPA, emailing [email protected], or calling the FDA at 1-800-FDA-1088

Patients receiving VASCEPA and concomitant anticoagulants and/or anti-platelet agents should be monitored for bleeding

Please see full Prescribing Information for more information on VASCEPA.

Capsule is not actual size.