Informational only — Not medical advice. Always consult a licensed healthcare provider.

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Other brands with the same active ingredient

These brands contain the same active ingredient (Armodafinil). Same strength and form. Confirm the switch with your doctor or pharmacist.

Indications & Uses

Uptiva is indicated to improve wakefulness in adult patients with- Obstructive sleep apnea (OSA) Narcolepsy Shift work disorder (SWD)

Dosage Reference

Reference Information Only

Dosages shown are general references from official sources. Always consult your doctor or pharmacist for personalized dosing.

Adults:

Adults: Obstructive Sleep Apnea & Narcolepsy: 150 mg to 250 mg as a single dose in the morning. Shift Work Disorder: 150 mg as a single dose approximately 1 hour prior to the start of work shift. Children: Safety and effectiveness in pediatric patients less than 17 years of age have not been established.Elderly: In elderly patients, elimination of Armodafinil and its metabolites may be reduced as a consequence of aging. Therefore, consideration should be given to the use of lower doses and close monitoring in this population.

Side Effects

The most common side effects of Uptiva are serious rash, including Stevens-Johnson syndrome, angioedema and anaphylaxis reactions, multi-organ hypersensitivity reactions, persistent sleepiness, psychiatric symptoms and some cardiovascular events.

Cautions & Contraindications

Warnings & Precautions

Patients should be cautioned about operating an automobile or other hazardous machinery until it is reasonably certain that Uptiva therapy will not adversely affect their ability to engage in such activities. Caution should be taken in treating patients with a history of psychosis, depression or mania. Discontinuation of treatment should be considered if psychiatric symptoms develop. Increased monitoring of heart rate and blood pressure should be exercised. Caution should be exercised when prescribing Uptiva to patients with known cardiovascular disease.

Contraindications

Contraindicated in patients with known hypersensitivity to Armodafinil or any of theexcipients of this product

Drug Interactions

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Last updated: 15 Aug 2026