Dormicum 7.5 mg Tablet contains Midazolam, a short-acting benzodiazepine used for the short-term treatment of insomnia and as a sedative premedication before surgical or diagnostic procedures. It produces rapid sedation, muscle relaxation, anxiolysis, and amnesia, making it widely used in both hospital and clinical settings.
Dormicum acts quickly and has a relatively short duration of action, which makes it suitable for temporary sleep disturbances and procedural sedation under medical supervision.
রেজিস্টার্ড চিকিৎসকের পরামর্শ অনুযায়ী ঔষধ সেবন করুন
Benzodiazepine hypnotics
Benzodiazepine sedatives
Dormicum 7.5 mg binds selectively to benzodiazepine receptors located on postsynaptic GABA-A receptors in the central nervous system, including the limbic system and reticular formation.
It enhances the inhibitory effect of gamma-aminobutyric acid (GABA) by increasing chloride ion permeability across neuronal membranes. This leads to:
Hyperpolarization of neurons
Reduced neuronal excitability
Sedation and anxiolysis
Muscle relaxation
Induction of sleep and amnesia
Its rapid onset and short half-life make it particularly useful for procedural sedation and short-term management of insomnia.
Dormicum 7.5 mg is indicated for:
Short-term treatment of insomnia
Premedication before surgical or diagnostic procedures
Sedation for endoscopic and cardiovascular procedures
Induction of anesthesia
Adults (Insomnia): 7.5–15 mg daily
Elderly and debilitated patients: 7.5 mg daily
Premedication: 7.5–15 mg given 30–60 minutes before procedure
Treatment duration should generally not exceed 2 weeks. Extension beyond this period requires medical supervision.
Endoscopic/Cardiovascular procedures:
Healthy adults: Initial dose 2.5 mg IV
Elderly/debilitated: 1–1.5 mg IV
Induction of anesthesia (Adults): 10–15 mg IV
Adults: 0.07–0.1 mg/kg (usual dose ~5 mg)
Children: 0.15–0.20 mg/kg
Elderly/debilitated: 0.025–0.05 mg/kg
0.35–0.45 mg/kg, 20–30 minutes before induction of anesthesia
IV administration should be given very slowly to minimize respiratory depression risk.
Dormicum enhances the sedative effects of:
Neuroleptics
Tranquilizers
Antidepressants
Hypnotics
Opioid analgesics
Anesthetics
Antipsychotics
Antiepileptics
Sedative antihistamines
Concurrent use increases risk of excessive sedation and respiratory depression.
Dormicum 7.5 mg must not be used in patients with:
Severe respiratory insufficiency
Severe hepatic insufficiency
Myasthenia gravis
Sleep apnea syndrome
Known hypersensitivity to benzodiazepines
Common side effects at the beginning of therapy may include:
Daytime drowsiness
Confusion
Fatigue
Headache
Muscle weakness
Following IV or IM administration, fluctuations in vital signs may occur, including:
Respiratory depression
Apnea
Changes in blood pressure and pulse rate
Severe overdose may cause:
Coma
Areflexia
Cardiorespiratory depression
Apnea
Effects may be reversed with flumazenil, a benzodiazepine antagonist.
Administer IV doses slowly
Monitor respiratory and cardiovascular function during parenteral use
Use cautiously in elderly, debilitated, or medically compromised patients
Risk of dependence with prolonged use
Should be avoided during pregnancy unless no safer alternative exists
Benzodiazepines may adversely affect the fetus
Excreted in breast milk; not recommended during breastfeeding
Store in a cool, dry place
Protect from light and moisture
Keep out of reach of children
Dormicum 7.5 mg potentiates the action of GABA at GABA-A receptors, increasing chloride channel opening frequency and producing sedation, muscle relaxation, anxiolysis, hypnosis, anesthesia, and amnesia.
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