Armod

Armod

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Product dosage: 150 mg
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Synonyms

Armod: Enhance Wakefulness and Cognitive Function

Armod is a prescription medication specifically designed to promote wakefulness in individuals experiencing excessive daytime sleepiness associated with conditions such as narcolepsy, obstructive sleep apnea, and shift work sleep disorder. Its active ingredient, armodafinil, is the R-enantiomer of modafinil, offering a refined pharmacological profile with a longer half-life. This allows for sustained alertness and improved cognitive performance throughout waking hours, helping patients maintain a more normal daily routine. Clinically proven and widely trusted, Armod represents a significant advancement in the management of sleep-wake disorders, supporting both neurological function and overall quality of life.

Features

  • Contains armodafinil, the pharmacologically active R-enantiomer of modafinil
  • Extended half-life of approximately 15 hours for all-day wakefulness promotion
  • Available in 50 mg, 150 mg, and 250 mg tablet strengths
  • FDA-approved for treating excessive sleepiness due to narcolepsy, obstructive sleep apnea, and shift work disorder
  • Low potential for abuse compared to traditional stimulants
  • Minimal impact on dopamine reuptake, reducing risk of euphoria or dependence

Benefits

  • Promotes sustained wakefulness and alertness during desired hours
  • Enhances cognitive functions including memory, attention, and executive function
  • Helps improve overall productivity and ability to perform daily tasks
  • Supports a more regular sleep-wake cycle without causing significant nighttime insomnia when dosed appropriately
  • Reduces the frequency of unintended sleep episodes in diagnosed sleep disorders
  • Generally well-tolerated with a favorable side effect profile for long-term use

Common use

Armod is primarily prescribed for the treatment of excessive daytime sleepiness in adult patients diagnosed with narcolepsy, obstructive sleep apnea (OSA) (as adjunctive therapy to continuous positive airway pressure, or CPAP), and shift work sleep disorder. In clinical settings, it may also be used off-label to address fatigue related to other medical conditions such as multiple sclerosis or depression, though such use should be carefully supervised by a healthcare provider. It is not indicated for use in pediatric populations or for improving sleep in individuals without a diagnosed sleep disorder.

Dosage and direction

The recommended dosage of Armod is individualized based on the condition being treated and patient response. For narcolepsy or obstructive sleep apnea, the typical dose is 150 mg or 250 mg taken orally once daily in the morning. For shift work sleep disorder, 150 mg is taken approximately one hour before the start of the work shift. It may be taken with or without food, though taking it with food may delay onset of action. Dosage adjustments may be necessary in patients with severe hepatic impairment, with a recommended starting dose of 50 mg. Do not crush or chew tablets; swallow whole with water.

Precautions

Patients should use Armod under strict medical supervision. It is important to note that while Armod promotes wakefulness, it does not replace adequate sleep. Avoid activities requiring mental alertness, such as driving or operating machinery, until the individual’s response to the drug is known. Use with caution in patients with a history of psychosis, depression, mania, or cardiovascular disease. Regular monitoring of blood pressure and heart rate is advised during treatment. Armod may reduce the effectiveness of hormonal contraceptives; alternative or additional methods of contraception should be used during and for one month after discontinuation.

Contraindications

Armod is contraindicated in patients with known hypersensitivity to armodafinil, modafinil, or any component of the formulation. It should not be used in patients with a history of left ventricular hypertrophy or ischemic ECG changes, chest pain, arrhythmias, or other significant cardiac conditions. Use is also contraindicated in those with a history of symptomatic mitral valve prolapse. Not recommended during pregnancy or breastfeeding unless the potential benefit justifies the potential risk to the fetus or infant.

Possible side effect

Common side effects may include headache, nausea, dizziness, insomnia, anxiety, and dry mouth. Less frequently, patients may experience palpitations, increased blood pressure, diarrhea, or nervousness. Rare but serious side effects can include severe skin reactions (e.g., Stevens-Johnson syndrome), psychiatric symptoms such as aggression or depression, hallucinations, or signs of allergic reaction (e.g., swelling, difficulty breathing). Patients should seek immediate medical attention if they experience chest pain, suicidal thoughts, or a serious rash.

Drug interaction

Armod can interact with several medications. It may induce CYP3A4/5 enzymes, potentially reducing the plasma concentrations of drugs such as cyclosporine, midazolam, triazolam, and certain hormonal contraceptives. Conversely, strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole) may increase armodafinil levels. Use with monoamine oxidase inhibitors (MAOIs) is not recommended. Caution is advised when co-administering with drugs that affect serotonin (e.g., SSRIs, SNRIs) due to potential serotonin syndrome risk. Inform your healthcare provider of all medications, including over-the-counter drugs and supplements.

Missed dose

If a dose of Armod is missed, it should be taken as soon as remembered unless it is close to the time of the next scheduled dose. In that case, skip the missed dose and resume the usual dosing schedule. Do not double the dose to make up for a missed one, as this may increase the risk of side effects. If uncertain, patients should consult their healthcare provider or pharmacist for guidance.

Overdose

Symptoms of Armod overdose may include insomnia, central nervous system excitation such as restlessness, disorientation, confusion, agitation, anxiety, tachycardia, hypertension, and nausea. In cases of suspected overdose, seek immediate medical attention or contact a poison control center. Treatment is symptomatic and supportive; there is no specific antidote. Ensure adequate hydration and monitor cardiac and vital signs closely.

Storage

Store Armod tablets at room temperature, between 20°C to 25°C (68°F to 77°F), in a tightly closed container. Keep away from moisture, light, and excessive heat. Do not store in the bathroom or near the kitchen sink. Keep out of reach of children and pets. Dispose of unused or expired medication in accordance with local regulations, preferably through a medicine take-back program.

Disclaimer

This information is intended for educational purposes only and does not replace professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before starting, changing, or discontinuing any medication or treatment plan. Individual responses to medication may vary. Do not use Armod without a valid prescription and appropriate medical supervision.

Reviews

“Since starting Armod for my shift work disorder, I’ve noticed a significant improvement in my ability to stay alert and focused during night shifts. It has made a real difference in my job performance and overall well-being.” – Mark T., verified patient

“As a sleep specialist, I find Armod to be a reliable option for patients who need sustained wakefulness without the peaks and troughs associated with other stimulants. It integrates well into comprehensive treatment plans for sleep disorders.” – Dr. Elena R., neurologist

“I was initially concerned about side effects, but Armod has been well-tolerated for me. I take it for narcolepsy, and it helps me get through the day without unexpected sleep attacks.” – Sophia L., long-term user