GNH USA

Europe — EMA

Lendormin

GNH USA supplies Lendormin (Brotizolam), a benzodiazepine sedative‑hypnotic for insomnia and sleep disorders. Request a quote for global supply today.

Brotizolam

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What is Brotizolam?

Brotizolam, the active ingredient in Lendormin, is a benzodiazepine presented as an oral tablet for oral use. It is prescribed to manage insomnia and other sleep disorders in adult patients who require short‑term sedative‑hypnotic therapy.

GNH USA supplies Lendormin as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable sourcing for regulated markets across Europe, Asia and the Americas. Customers benefit from comprehensive documentation, batch traceability and responsive technical support throughout the procurement process.

What is Brotizolam used for?

Brotizolam is used as a sedative‑hypnotic for disorders affecting sleep initiation and maintenance. - Insomnia: Improves sleep onset and reduces nighttime awakenings in patients with difficulty maintaining sleep. - Primary sleep disorder: Provides short‑term relief of symptoms in diagnosed primary insomnia. - Sleep maintenance disorder: Helps sustain continuous sleep throughout the night for individuals with fragmented sleep patterns. - Sleep onset insomnia: Reduces latency to fall asleep in patients experiencing prolonged time to sleep. - Circadian rhythm sleep disorder: Assists in adjusting sleep timing when used under medical supervision.

What are the side effects of Brotizolam?

Brotizolam may cause a range of adverse reactions, varying from mild to severe.

Common Side Effects: - Drowsiness: Feeling of excessive sleepiness during daytime. - Dizziness: Light‑headed sensation or loss of balance. - Headache: Mild to moderate cranial pain. - Dry mouth: Reduced salivation leading to oral dryness. - Fatigue: Persistent feeling of low energy and tiredness. - Impaired coordination: Reduced motor control leading to clumsiness.

Serious or Rare Side Effects: - Respiratory depression: Marked reduction in breathing effort, especially with other depressants. - Dependence and withdrawal: Risk of physical dependence with prolonged use and possible withdrawal symptoms upon abrupt cessation. - Severe allergic reaction: Signs such as rash, itching, swelling, or anaphylaxis. - Paradoxical agitation: Unexpected increase in anxiety, aggression or restlessness. - Psychomotor slowing: Noticeable slowing of thought processes and reaction time. - Hepatic dysfunction: Elevated liver enzymes indicating possible liver stress.

What precautions apply to Brotizolam?

When prescribing Brotizolam, clinicians should observe several safety considerations to minimise risk. - Assess patient history: Review prior benzodiazepine exposure, dependence, or substance‑use disorders. - Avoid in severe hepatic impairment: Use with caution or consider alternative therapy. - Caution in elderly: Increased susceptibility to falls, confusion and prolonged sedation. - Do not combine with alcohol: Concomitant use can intensify central nervous system depression. - Pregnancy and lactation: Use only if benefits outweigh potential risks; discuss with obstetric provider. - Store at ambient temperature: Keep in original packaging, protect from moisture and light.

What does Brotizolam interact with?

Brotizolam can interact with other medicines, altering its sedative effect or safety profile.

Major Interactions (Avoid): - Alcohol: Potentiates central nervous system depression, increasing risk of respiratory compromise. - Opioids: Combined use may cause profound sedation, respiratory depression, and overdose. - Other benzodiazepines: Additive effects heighten sedation and psychomotor impairment. - Barbiturates: Synergistic depression of neuronal activity leading to severe CNS depression. - Antidepressants (e.g., tricyclics): May increase sedation and cardiovascular side effects.

Moderate Interactions (Monitor Closely): - CYP3A4 inhibitors (e.g., ketoconazole): Can raise Brotizolam plasma levels, requiring dose adjustment. - CYP3A4 inducers (e.g., rifampicin): May reduce drug exposure, potentially decreasing efficacy. - Antihistamines: May enhance drowsiness and impair alertness. - Antihypertensives: Possible additive hypotensive effect, monitor blood pressure. - Antipsychotics: May increase sedation; observe for excessive CNS depression.

Frequently asked questions

What is Lendormin used for?+
Lendormin contains the benzodiazepine brotizolam and is indicated for the short‑term treatment of insomnia and related sleep disorders. It helps patients fall asleep faster, reduces nighttime awakenings, and improves overall sleep quality when used under medical supervision.
How does Brotizolam work?+
Brotizolam binds to the benzodiazepine site on the GABA‑A receptor complex, acting as a positive allosteric modulator. This enhances the inhibitory effect of GABA, increasing chloride ion flow into neurons, which dampens neuronal firing and produces sedation, hypnosis, and anxiolysis.
What is the usual dose of Lendormin?+
The appropriate dose of Lendormin is determined by the prescribing clinician based on the individual’s age, severity of insomnia, liver function, and concomitant medications. Physicians typically start with the lowest effective dose and adjust as needed, following local prescribing guidelines.
Is Lendormin safe during pregnancy or breastfeeding?+
Safety data for brotizolam in pregnancy and lactation are limited. It should only be used when the potential benefit justifies the possible risk to the fetus or infant. Healthcare providers should discuss alternatives and closely monitor any pregnant or nursing patient who requires treatment.
How do I order Lendormin from GNH USA?+
To request Lendormin, submit an enquiry on the product page at gnh-usa.com specifying the required quantity. GNH USA works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any required import documentation.
How does Lendormin compare with other sedative‑hypnotics?+
Compared with non‑benzodiazepine hypnotics such as zolpidem, brotizolam has a similar rapid onset but a slightly longer half‑life, which may increase next‑day residual effects. Its benzodiazepine class also carries a higher risk of dependence and withdrawal, so clinicians often reserve it for short‑term use.
How should Lendormin be stored and handled?+
Lendormin tablets should be stored at ambient temperature, below 25 °C, in the original container to protect them from moisture and light. Keep the medication out of reach of children and do not use it after the expiration date printed on the package.
How is Lendormin administered?+
Lendormin is taken orally, usually with a glass of water, shortly before bedtime. The tablet should be swallowed whole and not chewed or crushed. Patients should follow the prescriber’s instructions regarding timing and whether it should be taken with or without food.
What are the most serious risks associated with Lendormin?+
The most serious risks include respiratory depression, especially when combined with other central nervous system depressants, the development of physical dependence and withdrawal symptoms after prolonged use, and rare severe allergic reactions such as anaphylaxis. Patients should be monitored closely for these events.
Who should not use Lendormin?+
Lendormin is contraindicated in individuals with known hypersensitivity to brotizolam or other benzodiazepines, severe respiratory insufficiency, acute narrow‑angle glaucoma, and patients with severe hepatic impairment. Caution is also advised for the elderly, pregnant women, and those with a history of substance misuse.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Brotizolam
Route
Oral Use
Manufacturer
Scs Boehringer Ingelheim Comm.V.
Origin
EU

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