The Cesamet Copay Card* provides INSTANT SAVINGS

Eligible insured patients can save up to $75 on the copay for each Cesamet prescription. Limit 6 prescriptions.

Get Your Copay Card

* Offer for eligible, insured patients only. For each prescription, eligible patient pays the plan copay amount up to $25. Offer covers balance of the copay above $25, if any (up to 120 capsules and a $75 savings per fill). Limit 6 fills per patient. See eligibility and exclusion information.

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Eligibility and Exclusion Information

Terms of Use

Subject to additional terms below, if you are an eligible patient, with a valid Cesamet prescription, you can use this card. You must deduct the value of this offer from any insurance reimbursement claim that you submit or that is submitted for you.

Eligibility and Exclusions

The card is not valid for prescriptions partly or fully reimbursable by Medicare (including Part D), Medicaid, CHAMPUS, TRICARE, DoD, VA, or other federal or state government programs (including patient assistance programs). This card is not valid for Massachusetts residents or where otherwise prohibited by law. This card is not valid for cash-paying patients or patients whose private health care or prescription plans pay the full cost of their prescriptions. This card cannot be combined with other Cesamet coupons, rebates, free trials, or offers.

Limitations

Subject to all applicable federal, state, and local laws. This card is not health insurance and is not transferable. Limit 1 card per patient during the offer period. This card is serialized and may not be reproduced. We are not responsible for lost, damaged, or misdirected mail.

This offer is the property of Meda Pharmaceuticals Inc. and OPUS Health, which reserve the right to rescind, revoke, or amend the offer program without notice. By using this card, you represent that you will comply with all terms and conditions of this program and your health insurance or prescription plan. We rely on that representation.

Please see Full Prescribing Information and see below for important risk information.

Cesamet Indication

  • Cesamet (nabilone) capsules are indicated for the treatment of the nausea and vomiting associated with cancer chemotherapy in patients who have failed to respond adequately to conventional antiemetic treatments.
  • This restriction in use is required because a substantial proportion of any group of patients treated with Cesamet can be expected to experience disturbing psychotomimetic reactions not observed with other antiemetic agents.
  • Because of its potential to alter the mental state, Cesamet is intended for use under circumstances that permit close supervision of the patient by a responsible individual, particularly during initial use and during dose adjustments.
  • Cesamet contains nabilone, which is a Schedule II controlled substance and has a high potential for abuse. Prescriptions for Cesamet should be limited to the amount necessary for a single cycle of chemotherapy (i.e., a few days).
  • Prescribers should monitor patients receiving nabilone for signs of excessive use, abuse, and misuse. Patients who may be at increased risk for substance abuse include those with a personal or family history of substance abuse or mental illness.
  • Cesamet capsules are not intended to be used on an as-needed basis or as a first antiemetic product prescribed for a patient.

Important Risk Information

  • Cesamet (nabilone) is contraindicated in any patient who has a history of hypersensitivity to any cannabinoid.
  • The effects of Cesamet may persist for a variable and unpredictable period of time following its oral administration. Adverse psychiatric reactions can persist for 48 to 72 hours following cessation of treatment.
  • Cesamet has the potential to affect the CNS, which might manifest itself in dizziness, drowsiness, euphoria (feeling "high"), ataxia, anxiety, disorientation, depression, hallucinations, and psychosis.
  • Since Cesamet can cause tachycardia and orthostatic hypotension, it should be used with caution in the elderly and in patients with hypertension or heart disease.
  • Because of individual variation in response and tolerance to the effects of Cesamet, patients should remain under supervision of a responsible adult, especially during initial use of Cesamet and during dose adjustments.
  • Patients receiving treatment with Cesamet should be specifically warned not to drive, operate machinery, or engage in any hazardous activity while receiving Cesamet.
  • Cesamet should not be taken with alcohol, sedatives, hypnotics, or other psychoactive substances because these substances can potentiate the central nervous system effects of nabilone.
  • Cesamet should also be used with caution in patients with current or previous psychiatric disorders (including manic depressive illness, depression, and schizophrenia), as the symptoms of these disease states may be unmasked by the use of cannabinoids.
  • Cesamet is a Schedule II controlled substance and should be used with caution in patients with a history of substance abuse, including alcohol abuse or dependence and marijuana use, since Cesamet contains a similar active compound to marijuana.
  • Cesamet has not been studied in pregnant patients, nursing mothers, or pediatric patients, and, therefore, if used at all in those populations, it should be used with caution.
  • The effects of QT prolongation potential by Cesamet have not been determined.
  • During controlled clinical trials, virtually all patients experienced at least one adverse reaction. The most commonly encountered events were drowsiness, vertigo, dry mouth, euphoria, ataxia, headache, and concentration difficulties.

Important Risk Information

  • Cesamet (nabilone) is contraindicated in any patient who has a history of hypersensitivity to any cannabinoid.
  • The effects of Cesamet may persist for a variable and unpredictable period of time following its oral administration. Adverse psychiatric reactions can persist for 48 to 72 hours following cessation of treatment.
  • Cesamet has the potential to affect the CNS, which might manifest itself in dizziness, drowsiness, euphoria (feeling "high"), ataxia, anxiety, disorientation, depression, hallucinations, and psychosis.
  • Since Cesamet can cause tachycardia and orthostatic hypotension, it should be used with caution in the elderly and in patients with hypertension or heart disease.
  • Because of individual variation in response and tolerance to the effects of Cesamet, patients should remain under supervision of a responsible adult, especially during initial use of Cesamet and during dose adjustments.
  • Patients receiving treatment with Cesamet should be specifically warned not to drive, operate machinery, or engage in any hazardous activity while receiving Cesamet.
  • Cesamet should not be taken with alcohol, sedatives, hypnotics, or other psychoactive substances because these substances can potentiate the central nervous system effects of nabilone.
  • Cesamet should also be used with caution in patients with current or previous psychiatric disorders (including manic depressive illness, depression, and schizophrenia), as the symptoms of these disease states may be unmasked by the use of cannabinoids.
  • Cesamet is a Schedule II controlled substance and should be used with caution in patients with a history of substance abuse, including alcohol abuse or dependence and marijuana use, since Cesamet contains a similar active compound to marijuana.
  • Cesamet has not been studied in pregnant patients, nursing mothers, or pediatric patients, and, therefore, if used at all in those populations, it should be used with caution.
  • The effects of QT prolongation potential by Cesamet have not been determined.
  • During controlled clinical trials, virtually all patients experienced at least one adverse reaction. The most commonly encountered events were drowsiness, vertigo, dry mouth, euphoria, ataxia, headache, and concentration difficulties.

Cesamet Indication

  • Cesamet (nabilone) capsules are indicated for the treatment of the nausea and vomiting associated with cancer chemotherapy in patients who have failed to respond adequately to conventional antiemetic treatments.
  • This restriction in use is required because a substantial proportion of any group of patients treated with Cesamet can be expected to experience disturbing psychotomimetic reactions not observed with other antiemetic agents.
  • Because of its potential to alter the mental state, Cesamet is intended for use under circumstances that permit close supervision of the patient by a responsible individual, particularly during initial use and during dose adjustments.
  • Cesamet contains nabilone, which is a Schedule II controlled substance and has a high potential for abuse. Prescriptions for Cesamet should be limited to the amount necessary for a single cycle of chemotherapy (i.e., a few days).
  • Prescribers should monitor patients receiving nabilone for signs of excessive use, abuse, and misuse. Patients who may be at increased risk for substance abuse include those with a personal or family history of substance abuse or mental illness.
  • Cesamet capsules are not intended to be used on an as-needed basis or as a first antiemetic product prescribed for a patient.