Rozerem (ramelteon)

Hypnotics Oral Tablet

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Last reviewed · Source: First Databank (FDB) drug data

Overview

Ramelteon, a melatonin receptor agonist, is a hypnotic agent.

Ramelteon, a melatonin receptor agonist, is a hypnotic agent. The drug exhibits high affinity for melatonin MT1 and MT2 receptors. The agonist activity of ramelteon at these receptors is thought to contribute to the drug's sleep-inducing properties, as stimulation of these receptors by endogenous melatonin is thought to be responsible for the regulation of circadian rhythm underlying the normal sleep-wake cycle.

Ramelteon demonstrates lower selectivity for melatonin MT3 receptors than for MT1 and MT2 receptors; the drug has no appreciable affinity for the gamma-aminobutyric acid (GABA) receptor complex or for receptors that bind neuropeptides, cytokines, serotonin, dopamine, norepinephrine, acetylcholine, or opiates.

Ramelteon is rapidly absorbed and undergoes extensive first-pass metabolism. Following oral administration in the fasting state, peak ramelteon concentrations occur at approximately 0.75 hours (range: 0.5-1.5 hours). Although total absorption of ramelteon is at least 84%, the absolute bioavailability is only 1.8% due to extensive first-pass metabolism.

Administration with a high-fat meal delays GI absorption, reduces peak plasma concentration, and increases the area under the plasma-concentration time curve (AUC) of ramelteon. Ramelteon is extensively distributed to tissues; the drug is approximately 82% bound to human serum proteins (mainly (70%) albumin).

Ramelteon is metabolized by the cytochrome P-450 (CYP) microsomal enzyme system, principally by CYP1A2 and, to a lesser extent, by the CYP2C subfamily and by CYP3A4 to active (M-II) and inactive metabolites. The elimination half-life of ramelteon or M-II is 1-2.6 or 2-5 hours, respectively. Following oral administration of radiolabeled ramelteon, approximately 84% of the radioactivity is eliminated in urine and 4% is eliminated in feces, principally as metabolites.

USES: This medication is used to treat sleeplessness (insomnia). It helps you fall asleep faster so you can get a full night's rest. Sleep is important for your ability to function, think clearly, and remain alert.

Lack of sleep can cause problems such as depression, heart disease and accidents. Getting enough sleep allows your mind and body to repair itself and increases your energy throughout the day. Ramelteon works like a natural substance called melatonin that is produced by your body.

It helps regulate your sleep-wake cycle (circadian rhythm).

Generic name: ramelteon
Pronunciation: (ra-MEL-tee-on)
Drug class: Hypnotics
Therapeutic class: Central Nervous System Agents

Reference product & biosimilars

No reference, biosimilar or interchangeable associated with this drug.

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Indications

The following indications are listed for Rozerem:

  • Sleep-Onset Insomnia

Also known as: Insomnia Due To Delayed Sleep Onset, Insomnia Due To Increased Sleep Latency.

Dosing

The recommended adult dosage of ramelteon for the management of insomnia is 8 mg within 30 minutes of bedtime.

Drug interactions

There is no enhanced messaging for this drug.

Contraindications

Hypersensitivity to ramelteon or any ingredient in the formulation.

Adverse reactions

Adverse effects reported in 2% or more of patients receiving ramelteon during clinical trials include headache, somnolence, fatigue, dizziness, nausea, exacerbation of insomnia, upper respiratory tract infection, diarrhea, myalgia, depression, dysgeusia, and arthralgia.

Precautions

No enhanced messaging available.

ICD codes

CodeTypeDescription
Sleep-onset insomnia
F51.01ICD10CMPrimary insomnia
G47.00ICD10CMInsomnia, unspecified

ICD code information from First Databank (FDB).

Formulary status

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Last reviewed · Source: First Databank (FDB) drug data