Product image of Modiodal (Modafinil) supplied by GNH India

Modiodal

Active Ingredient:
Modafinil
Origin:
EU

Modiodal (Modafinil)

Modafinil, the active ingredient in Modiodal, is a eugeroic (wakefulness‑promoting agent) presented as an oral tablet for oral use. It is indicated to reduce daytime sleepiness in adults with narcolepsy, obstructive sleep apnea‑related residual sleepiness, and shift work sleep disorder, helping improve alertness and functional performance.

GNH India supplies Modiodal as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Neuraxpharm Pharmaceuticals S.L.

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Indications & Clinical Uses

Modiodal (modafinil) promotes wakefulness in disorders characterized by excessive daytime sleepiness.

  • Narcolepsy: reduces sudden sleep attacks and improves daytime alertness.
  • Obstructive sleep apnea‑related excessive daytime sleepiness: lessens residual sleepiness despite optimal apnea therapy.
  • Shift work sleep disorder: helps maintain alertness during scheduled work hours.

How It Works

  • Modiodal works by inhibiting the reuptake of dopamine, thereby increasing extracellular dopamine concentrations in key brain regions. It also activates hypothalamic orexin neurons, which further enhances arousal pathways. The combined effect results in sustained wakefulness without the typical stimulant‑like surge in sympathetic activity.

Side Effects

Modiodal may cause a range of adverse reactions, which are generally categorized by frequency and severity.

Common Side Effects

  • Headache: mild to moderate discomfort often reported during the first weeks of therapy.
  • Nausea: transient gastrointestinal upset that usually resolves with continued use.
  • Insomnia: difficulty falling or staying asleep, especially when taken later in the day.
  • Anxiety or nervousness: heightened sense of restlessness in some patients.

Serious or Rare Side Effects

  • Severe skin reactions (e.g., Stevens‑Johnson syndrome): requires immediate medical attention.
  • Psychiatric events (e.g., mania, depression, hallucinations): monitor patients with pre‑existing mental health conditions.
  • Cardiovascular events (e.g., hypertension, arrhythmia): seek urgent care if chest pain or palpitations occur.

Precautions & Warnings

Before initiating Modiodal, clinicians should consider several safety measures.

  • Assess cardiovascular status: evaluate blood pressure and heart disease history.
  • Avoid use in patients with known hypersensitivity to modafinil or its excipients.
  • Monitor for psychiatric symptoms: watch for new or worsening depression, mania, or psychosis.
  • Consider dose adjustment in hepatic impairment: reduced clearance may increase exposure.
  • Pregnancy and lactation: use only if the potential benefit outweighs the risk.
  • Store at ambient temperature below 25°C: keep in the original pack, protect from moisture.

Avoid Interactions

Modiodal can interact with other medicines, affecting its efficacy or safety.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, erythromycin): may raise modafinil plasma levels.
  • CNS depressants (e.g., benzodiazepines): may diminish the wake‑promoting effect.
  • CYP3A4 inducers (e.g., carbamazepine, phenytoin): may lower modafinil concentrations and reduce effectiveness.

Moderate Interactions (Monitor Closely)

  • Oral contraceptives: modafinil may reduce hormonal contraceptive efficacy.
  • Antidepressants (especially SSRIs): increased risk of serotonin‑related adverse events.
  • Alcohol: may enhance central nervous system side effects such as dizziness or headache.

Frequently Asked Questions

Modiodal contains modafinil, a wakefulness‑promoting agent indicated to reduce excessive daytime sleepiness in adults with narcolepsy, obstructive sleep apnea‑related residual sleepiness, and shift work sleep disorder. It helps improve alertness and functional performance during waking hours.

Modafinil primarily inhibits the reuptake of dopamine, increasing its concentration in brain regions that regulate arousal. It also stimulates hypothalamic orexin neurons, further enhancing wake‑promoting pathways without the strong sympathomimetic effects seen with traditional stimulants.

The appropriate dose of Modiodal is determined by the prescribing clinician based on the individual’s condition, response, and tolerability. Dosage may be adjusted over time, and patients should follow the prescriber’s instructions without self‑adjusting the regimen.

Modiodal is classified as a prescription‑only medication and should be used during pregnancy or lactation only if the potential benefit justifies the potential risk to the fetus or infant. Healthcare providers should discuss individual risks and consider alternative therapies when appropriate.

To request Modiodal, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Modiodal (modafinil) and its R‑enantiomer armodafinil share a similar mechanism of inhibiting dopamine reuptake, but armodafinil may have a slightly longer half‑life. Compared with traditional stimulants such as methylphenidate, modafinil generally produces less cardiovascular stimulation and lower abuse potential.

Modiodal tablets should be stored at ambient temperature below 25 °C, in the original container, and protected from moisture and direct sunlight. Keep the product out of reach of children and do not use it after the expiration date.

Modiodal is taken orally, usually with a glass of water. It is commonly taken once daily in the morning for narcolepsy or obstructive sleep apnea, and early in the work shift for shift‑work sleep disorder, to avoid interference with nighttime sleep.

Serious risks include severe skin reactions such as Stevens‑Johnson syndrome, psychiatric events like mania or depression, and cardiovascular problems such as hypertension or arrhythmia. Patients should seek immediate medical attention if they notice rash, mood changes, chest pain, or palpitations.

Modiodal is contraindicated in individuals with known hypersensitivity to modafinil or any of its excipients. Caution is advised for patients with uncontrolled hypertension, significant cardiac disease, severe hepatic impairment, or a history of psychiatric disorders, and it should be avoided in these populations unless specifically directed by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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