618PM

Tyler, a real patient with narcolepsy on LUMRYZ,
more awake to study after class

Tyler was compensated by Alkermes.
Individual results may vary.

Tyler, a real patient, studying in a library.

Extended-release LUMRYZ is dosed once at bedtime1

Its innovative oxybate formula delivers treatment throughout your patient’s nocturnal sleep period1,2

Pouring lumryz into a container.

Patients take 1 packet at bedtime. ​1

LUMRYZ is available in the following dose strengths: 4.5, 6, 7.5, and 9 grams.1

Each premeasured packet contains a full therapeutic dose, supporting consistent dosing.1,3

LUMRYZ dosing information

Lumryz pouches come in different colors.

Once-at-bedtime, premeasured packets contain your patient’s full therapeutic dose, supporting consistent dosing1,3

Doses are available in 4.5 g, 6 g, 7.5 g, and 9 g packets.1

Icon of a hand pouring a single packet of Lumryz.

LUMRYZ is taken orally as a single dose at bedtime1

  • Mix 1 premeasured packet with water1,4*
    • If desired, patients can include a calorie-free drink mix or flavored water enhancer, such as Crystal Lite or Mio Flavored Water Enhancer  
Icon of the Lumryz granules.

Each dose contains a blend of immediate- and controlled-release granules1,2,5

  • Shake for 60 seconds—expect the granules to not fully dissolve in water* and have a gritty texture with a salty taste5
Icon of a person in bed.

LUMRYZ should be taken at least 2 hours after eating and when in bed1

  • Patients may fall asleep within 5 to 15 minutes of taking their dose without feeling drowsy
  • Advise the patient to read the FDA-approved patient labeling (Medication Guide and Instructions for Use) for full administration instructions.
  • *Do not use hot water.4

These instructions are not complete. Download Instructions for Use for complete administration directions.

Tyler, a real patient, holding a basketball and talking to someone in a library.

Information to share with patients as they begin treatment

Support successful patient starts

Tyler is a real patient, compensated by Alkermes.

Choose the titration process that best fits your patients’ needs

Titrate gradually to a dose that best fits your patients’ needs based on efficacy and tolerability1

  • After starting at 4.5 g per night, you may increase by 1.5 g increments per week, or you may increase more gradually based on efficacy and tolerability

Titrate gradually to a dose that best fits their needs1

  • Start on the 4.5 g once per night and then increase by 1.5 per night at weekly intervals to the maximum recommended dosage of 9 g once per night orally 

Extended-release LUMRYZ is the first and only single-dose oxybate approved for pediatric use (ages  ≥7)1

Select the nearest equivalent dose of LUMRYZ

  • For example, 7.5 g of LUMRYZ is approximately 2 doses of 3.75 g twice-nightly oxybate 

Are your patients missing their second dose? 

To ensure an appropriate starting dose for patients switching to LUMRYZ, consider asking how frequently they miss the second dose of their current twice-nightly therapy. 

Select the nearest equivalent dose of LUMRYZ1

  • Because the recommended starting dosage in pediatric patients 7 years and older weighing less than 45 kg (99 lb) cannot be achieved with the available strengths of LUMRYZ, use another sodium oxybate product to initiate treatment. Refer to the Prescribing Information of other sodium oxybate products for the recommended dosage for those products
  • Pediatric patients ≥20 kg (44 lb) can be switched to LUMRYZ if they are taking a 4.5 g dose or higher of another oxybate. The dose may be gradually titrated based on efficacy and tolerability
  • The maximum recommended dosage for patients 7 years and older weighing 20 kg to <30 kg is 6 g once per night orally
  • The maximum recommended dosage for patients 7 years and older weighing 30 kg to <45 kg is 7.5 g once per night orally
  • There is insufficient information to provide specific dosing recommendations for patients 7 years and older who weigh less than 20 kg

What might it mean for family and care partners to not wake to administer a middle-of-the-night dose?

For patients new to LUMRYZ

It’s important to let patients know that everybody responds to treatment differently and it may take time to see a difference in their daytime symptoms as their body adjusts to the medicine.

Icon of a hand holding some information documents.

Find downloadable content and other resources for starting LUMRYZ​

Visit resource center

LUMRYZ dosing information

Lumryz pouches come in different colors.

Once-at-bedtime, premeasured packets contain your patient’s full therapeutic dose, supporting consistent dosing1,3

Doses are available in 4.5 g, 6 g, 7.5 g, and 9 g packets.1

Icon of a hand pouring a single packet of Lumryz.

LUMRYZ is taken orally as a single dose at bedtime1

  • Mix 1 premeasured packet with water1,4*
    • If desired, patients can include a calorie-free drink mix or flavored water enhancer, such as Crystal Lite or Mio Flavored Water Enhancer  
Icon of the Lumryz granules.

Each dose contains a blend of immediate- and controlled-release granules1,2,5

  • Shake for 60 seconds—expect the granules to not fully dissolve in water* and have a gritty texture with a salty taste5
Icon of a person in bed.

LUMRYZ should be taken at least 2 hours after eating and when in bed1

  • Patients may fall asleep within 5 to 15 minutes of taking their dose without feeling drowsy
  • Advise the patient to read the FDA-approved patient labeling (Medication Guide and Instructions for Use) for full administration instructions.
  • *Do not use hot water.4

These instructions are not complete. Download Instructions for Use for complete administration directions.

Tyler, a real patient, holding a basketball and talking to someone in a library.

Information to share with patients as they begin treatment

Support successful patient starts

Tyler is a real patient, compensated by Alkermes.

Choose the titration process that best fits your patients’ needs

Titrate gradually to a dose that best fits your patients’ needs based on efficacy and tolerability1

  • After starting at 4.5 g per night, you may increase by 1.5 g increments per week, or you may increase more gradually based on efficacy and tolerability

Titrate gradually to a dose that best fits their needs1

  • Start on the 4.5 g once per night and then increase by 1.5 per night at weekly intervals to the maximum recommended dosage of 9 g once per night orally 

Extended-release LUMRYZ is the first and only single-dose oxybate approved for pediatric use (ages  ≥7)1

Select the nearest equivalent dose of LUMRYZ

  • For example, 7.5 g of LUMRYZ is approximately 2 doses of 3.75 g twice-nightly oxybate 

Are your patients missing their second dose? 

To ensure an appropriate starting dose for patients switching to LUMRYZ, consider asking how frequently they miss the second dose of their current twice-nightly therapy. 

Select the nearest equivalent dose of LUMRYZ1

  • Because the recommended starting dosage in pediatric patients 7 years and older weighing less than 45 kg (99 lb) cannot be achieved with the available strengths of LUMRYZ, use another sodium oxybate product to initiate treatment. Refer to the Prescribing Information of other sodium oxybate products for the recommended dosage for those products
  • Pediatric patients ≥20 kg (44 lb) can be switched to LUMRYZ if they are taking a 4.5 g dose or higher of another oxybate. The dose may be gradually titrated based on efficacy and tolerability
  • The maximum recommended dosage for patients 7 years and older weighing 20 kg to <30 kg is 6 g once per night orally
  • The maximum recommended dosage for patients 7 years and older weighing 30 kg to <45 kg is 7.5 g once per night orally
  • There is insufficient information to provide specific dosing recommendations for patients 7 years and older who weigh less than 20 kg

What might it mean for family and care partners to not wake to administer a middle-of-the-night dose?

For patients new to LUMRYZ

It’s important to let patients know that everybody responds to treatment differently and it may take time to see a difference in their daytime symptoms as their body adjusts to the medicine.

Icon of a hand holding some information documents.

Find downloadable content and other resources for starting LUMRYZ​

Visit resource center

I like the dosing packets for LUMRYZ because I don’t have to measure it myself. It allows me to just focus on mixing my dose and not having to measure the right amount of medication.”

-Tyler

Hear what patients have to say about LUMRYZ

Watch patient videos

Tyler was compensated by Alkermes. Individual results may vary.

References: 1. LUMRYZ® (sodium oxybate for extended-release oral suspension). Prescribing Information. Chesterfield, MO: Avadel Pharmaceuticals. 2. Bogan R, Thorpy MJ, Winkelman JW, Dubow J, Gudeman J, Seiden D. Randomized, crossover, open-label study of the relative bioavailability and safety of FT218, a once-nightly sodium oxybate formulation: phase 1 study in healthy volunteers. Sleep Med. 2022;100:442-447. 3. Seiden D, Tyler C, Dubow J. Pharmacokinetics of FT218, a once-nightly sodium oxybate formulation in healthy adults. Clin Ther. 2021;43(4):672.el-672.e14. 4. LUMRYZ. Instructions for Use. Chesterfield, MO: Avadel Pharmaceuticals; 2025. 5. Kushida CA, Shapiro CM, Roth T, et al. Once-nightly sodium oxybate (FT218) demonstrated improvement of symptoms in a phase 3 randomized clinical trial in patients with narcolepsy. Sleep. 2022;45(6):1-11.