Product image of Melatonina Aurovitas (Melatonin) supplied by GNH India

Melatonina Aurovitas

Active Ingredient:
Melatonin
Origin:
EU

Melatonina Aurovitas (Melatonin)

Melatonin, the active ingredient in Melatonina Aurovitas, is a melatonin receptor agonist presented as an oral formulation for oral use. It is employed to support the regulation of circadian rhythm and to promote sleep onset in adults experiencing sleep disturbances.

GNH India supplies Melatonina Aurovitas as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The product conforms to EU quality standards, is manufactured under GMP conditions, and is distributed through regulated channels to ensure product integrity and traceability.

Manufacturer / TM Owner

Aurovitas Spain,s.A.U.

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Indications & Clinical Uses

  • Melatonina Aurovitas acts on the melatonin pathway to address sleep‑related disorders.
  • Insomnia: helps initiate and maintain sleep in individuals with difficulty falling asleep.
  • Delayed sleep phase disorder: assists in advancing sleep timing to a more conventional schedule.
  • Jet lag: reduces the time required to adjust the internal clock after rapid time‑zone travel.

How It Works

  • Melatonin binds to MT1 and MT2 receptors in the suprachiasmatic nucleus, mimicking endogenous melatonin. This interaction synchronizes the circadian clock, lowers core body temperature, and promotes the physiological processes that facilitate sleep onset and maintenance without directly inducing sedation.

Side Effects

Melatonina Aurovitas may be associated with several adverse reactions.

Common Side Effects

  • Headache: mild to moderate intensity.
  • Dizziness: transient sensation of light‑headedness.
  • Daytime sleepiness: feeling unusually drowsy during waking hours.
  • Nausea: mild gastrointestinal discomfort.
  • Vivid dreams: unusually intense or memorable dreaming.
  • Mild abdominal discomfort: occasional stomach upset.

Serious or Rare Side Effects

  • Allergic reaction: rash, itching, or angioedema requiring medical attention.
  • Depression: worsening mood or depressive symptoms.
  • Seizures: rare occurrence in predisposed individuals.
  • Hormonal effects: potential impact on reproductive hormone balance.
  • Severe hypersensitivity: anaphylaxis requiring emergency care.

Precautions & Warnings

When considering Melatonina Aurovitas, several safety measures should be observed.

  • Evaluate sleep hygiene: ensure non‑pharmacologic measures are optimized before use.
  • Avoid use in shift‑work schedules: may interfere with circadian adaptation.
  • Monitor in patients with depression: melatonin can influence mood.
  • Use caution in the elderly: increased risk of falls due to daytime drowsiness.
  • Store at ambient temperature: keep in the original pack, protect from moisture and light.

Avoid Interactions

Melatonin can interact with various medicines; awareness of the interaction level is important.

Major Interactions (Avoid)

  • CNS depressants (e.g., benzodiazepines): may enhance sedation.
  • Anticoagulants (e.g., warfarin): potential alteration of bleeding risk.
  • Immunosuppressants (e.g., cyclosporine): may affect drug concentrations.

Moderate Interactions (Monitor Closely)

  • Oral contraceptives: melatonin may reduce contraceptive efficacy.
  • Antihypertensives: additive blood‑pressure‑lowering effect.
  • Caffeine: may diminish melatonin’s sleep‑promoting action.

Frequently Asked Questions

Melatonina Aurovitas is used to support the management of sleep disorders. It helps individuals who have difficulty falling asleep, experience delayed sleep phase, or need to adjust their internal clock after rapid travel across time zones.

Melatonin acts as an agonist at MT1 and MT2 receptors in the brain’s master clock. By binding these receptors, it signals darkness, helping to synchronize the circadian rhythm and promote the physiological processes that lead to sleep onset.

The appropriate dose of Melatonina Aurovitas is determined by the prescribing healthcare professional based on the patient’s age, condition, and response. Dosage may vary, and the prescriber will provide specific instructions.

Safety data for melatonin use in pregnancy and lactation are limited. Healthcare providers should evaluate the risk‑benefit profile before prescribing to pregnant or nursing individuals, and it is generally used only when clearly needed.

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

Unlike many sedative hypnotics, melatonin works by aligning the body’s natural clock rather than directly depressing the central nervous system. This mechanism often results in fewer next‑day residual effects, making it a preferred option for circadian‑related sleep disturbances.

Store the product at ambient temperature, preferably below 25 °C. Keep it in the original container, protect it from moisture and direct sunlight, and ensure the packaging remains sealed until use.

Melatonina Aurovitas is taken orally. The tablet (or capsule) should be swallowed with water, typically shortly before the intended bedtime, following the dosing instructions provided by the prescriber.

Serious but rare risks include severe allergic reactions such as rash, angioedema, or anaphylaxis, as well as possible worsening of depressive symptoms or seizure activity in susceptible individuals. Immediate medical attention is required if these occur.

Individuals with known hypersensitivity to melatonin, those taking interacting medications that cannot be safely managed, and patients with uncontrolled depression or seizure disorders should avoid using Melatonina Aurovitas unless a healthcare professional determines it is appropriate.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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