Thiontal Injection 500 mg/vial contains Thiopental Sodium, a rapid-acting barbiturate anesthetic widely used for the induction of general anesthesia and short-term sedation. It is known for its quick onset of action, producing unconsciousness within seconds after intravenous administration. This makes it highly suitable for use in surgical procedures, emergency interventions, and critical care settings.
Thiopental Sodium acts on the central nervous system to induce sedation, hypnosis, and anesthesia. Due to its short duration of action, it is commonly used as an induction agent before maintenance anesthesia is continued with other agents. Thiontal Injection is administered only by trained healthcare professionals in controlled medical environments such as hospitals and operating rooms.
রেজিস্টার্ড চিকিৎসকের পরামর্শ অনুযায়ী ঔষধ সেবন করুন
Rapid Induction of Anesthesia: Produces unconsciousness within seconds, ensuring quick procedural readiness.
Short Duration of Action: Allows for better control and quick recovery in short procedures.
Reliable Sedative Effect: Provides consistent and effective sedation in emergency and surgical settings.
Versatile Clinical Use: Suitable for anesthesia induction, seizure control, and intracranial pressure management.
Thiopental Sodium enhances the activity of gamma-aminobutyric acid (GABA), an inhibitory neurotransmitter in the brain. This leads to decreased neuronal excitability, resulting in sedation, hypnosis, and loss of consciousness. Its high lipid solubility allows rapid penetration into the brain, contributing to its fast onset.
Thiontal Injection 500 mg/vial is indicated for:
Induction of general anesthesia
Short surgical or diagnostic procedures
Control of certain types of seizures (e.g., status epilepticus)
Reduction of intracranial pressure in specific clinical conditions
Administered intravenously by qualified healthcare professionals only.
Dosage is individualized based on patient weight, age, and clinical condition.
Continuous monitoring of vital signs such as blood pressure, heart rate, and respiration is essential during administration.
Use with caution in patients with respiratory, cardiovascular, or liver disorders.
Contraindicated in patients with a history of acute porphyria.
Elderly and debilitated patients may require dose adjustments.
May interact with other central nervous system depressants, enhancing sedative effects.
Use during pregnancy only if clearly necessary and under strict medical supervision.
Possible side effects include:
Respiratory depression
Hypotension (low blood pressure)
Drowsiness or prolonged sedation
Nausea or vomiting
Serious adverse effects such as severe respiratory suppression or hypersensitivity reactions require immediate medical attention.
Store in a cool, dry place away from light and moisture. Keep out of reach of children. Ensure proper handling and use only under medical supervision.
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