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Armod (Armodafinil)

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Armod is currently FDA-approved to treat excessive daytime sleepiness associated with obstructive sleep apnea, narcolepsy, and shift work disorder. It is commonly used off-label to treat attention deficit hyperactivity disorder, chronic fatigue syndrome, and major depressive disorder. It has been shown to improve vigilance in air traffic controllers. Armod is approved by the U.S. FDA for the treatment of narcolepsy and shift work sleep disorder, and as an adjuvant therapy for obstructive sleep apnea. For narcolepsy and obstructive sleep apnea, Armod is taken as a once daily 150 mg or 250 mg dose in the morning. For shift work sleep disorder, 150 mg of Armod are taken one hour prior to starting work. Slow dose titration is needed to mitigate some side effects.

Other names for this medication:
Armod, Armodafinil, Biryth, Waklert

Similar Products:
Trileptal, Buspar, Neurontin, Flonase, Duricef, Diovan, Aldactone, Panadol

Also known as: Armodafinil


{name} (armodafinil) is a medication that promotes wakefulness.

{name} is used to treat excessive sleepiness caused by sleep apnea, narcolepsy, or shift work sleep disorder.


Take Armod exactly as prescribed by your doctor. Follow all directions on your prescription label. Do not take this medicine in larger or smaller amounts or for longer than recommended.

Armod may be habit-forming. Never share Armod with another person, especially someone with a history of drug abuse or addiction. Selling or giving away this medicine is against the law.

Read all patient information, medication guides, and instruction sheets provided to you. Ask your doctor or pharmacist if you have any questions.

Armod is usually taken each morning to prevent daytime sleepiness, or 1 hour before the start of a work shift to treat work-time sleep disorders.

You may take this medicine with or without food.

Armod is usually given for up to 12 weeks. Follow your doctor's instructions.

If you are taking this medicine to treat sleepiness caused by obstructive sleep apnea, you may also be treated with a continuous positive airway pressure (CPAP) machine. This machine is an air pump connected to mask that gently blows pressurized air into your nose while you sleep. The pump does not breathe for you, but the gentle force of air helps keep your airway open to prevent obstruction.

Do not stop using your CPAP machine during sleep unless your doctor tells you to. The combination of treatment with CPAP and Armod may be necessary to best treat your condition.

Taking this medication does not take the place of getting enough sleep. Talk with your doctor if you continue to have excessive sleepiness even while taking this medicine. Armod will not cure obstructive sleep apnea or treat its underlying causes. Follow your doctor's instructions about all your other treatments for this disorder.

Store at room temperature away from moisture and heat.

Keep track of the amount of medicine used from each new bottle. Armod is a drug of abuse and you should be aware if anyone is using your medicine improperly or without a prescription.

Detailed Armod dosage information


If you take too much Armod, call your healthcare provider or local Poison Control Center, or seek emergency medical attention right away.


Store Armod at 20 to 25 deegres C (68 to 77 degrees F).

Keep this and all medicines out of the reach of children.

Armod is classified as federally controlled substance (C-IV), because it can be abused or lead to dependence. Keep Armod in a safe place to prevent misuse and abuse.

Side effects

The most common side effects associated with Armod are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.


Armod may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert.

Avoid other dangerous activity until you know how this medication will affect your level of wakefulness.

Avoid drinking alcohol while taking Armod.

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To assess the anatomic feasibility of a median-to-radial nerve transfer in cadaver limbs and to quantify the number of axons present in the cut ends of the involved donor and recipient nerves. Infection of skin with Candida albicans is usually followed by infiltration of neutrophil granulocytes (PMN). The heritabilities for LMA, BF, and HCW were 0.13, 0.07, and 0.17, respectively, using matrix and 0.29, 0.16, and 0.23, respectively, using matrix . Scatchard analysis also shows that reoxygenated A431 cells display enhanced surface expression of the EGF-R compared with aerobic control cells. Mutations within the conserved NS1 nuclear export signal lead to inhibition of influenza A virus replication. Knockdown of microRNA-195 contributes to protein phosphatase-2A inactivation in rats with chronic brain hypoperfusion. Multiple clinical trials are underway to evaluate the antitumor activity of recombinant human TRAIL and agonistic antibodies to DR4 or DR5. Recently, the glucokinase gene locus on chromosome 7p has been shown to be linked to a subtype of NIDDM known as MODY in French and British pedigrees, and glucokinase mutations have been identified. In this article, we report the evidence that contributed to the implementation of pharmacokinetic pharmacogenetic guidelines for antidepressants primarily metabolized by CYP2D6 and CYP2C19.

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Changes in the hypophyseal-thyroid system under narcotic action in the parturients of a group at high risk of perinatal pathology. The aggressiveness of murine lymphomas selected in vivo by growth rate correlates with galectin-1 expression and response to cyclophosphamide. Many nanocomposites are intended to be pH-responsive as drug carriers because of a tumorous zyloprim allopurinol cost or intracellular mildly acidic environment. Dominance in RHO mutations is associated with two phenomena: interference with the function of normal rhodopsin and intrinsic toxicity of the mutant protein. In the validation phase, we assessed the psychometric properties of the instrument in a cross-sectional survey of 164 Korean women with breast cancer participating in self-support groups. L-Glutamate uptake adjusted to diffusion kinetics, with a Kd which did not change due to starvation. However, to date, there has been no review of evidence on the outcomes of social enterprise involvement in healthcare, nor in the ability of social enterprise to address health inequalities more widely through action on the social determinants of health. Primary biliary cirrhosis: increasing problem, approaching solution. Good selectivity, linearity, accuracy, precision and recovery were achieved, and no significant matrix effect was observed. Daytime sleep patterns in preschool children with autism, developmental delay, and typical development.

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