Dormitol IM/IV Injection 15 mg/3 ml is a benzodiazepine medication used to induce and maintain anaesthesia, aid in sedation for surgery or other medicinal procedures, and treat certain types of seizures, anxiety disorders, and insomnia. It is typically administered in intravenous, intramuscular, and oral form, and can cause drowsiness, confusion, and muscle relaxation depending on the dose.
| Brand Name | Dormitol |
|---|---|
| Type | IM/IV Injection |
| Weight | 15 mg/3 ml |
| Generic | Midazolam |
| Manufacturer | Square Pharmaceuticals Ltd. |
| Available in | English বাংলা |
Dormitol IM/IV Injection 15 mg/3 ml is a central nervous system (CNS) depressant that works primarily by activating the gamma-aminobutyric acid (GABA) receptor-chloride channel receptor complex. This interaction leads to increased chloride ion conductance, membrane hyperpolarization, and ultimately, the suppression of excitatory signaling. Additionally, it binds to benzodiazepine receptors which causes sedative, anxiolytic, and anticonvulsant activity.
The effects of midazolam can occur within minutes as it is rapidly and readily absorbed. Intestinal absorption is higher when it is injected intravenously compared to the intramuscular route.
Dormitol IM/IV Injection 15 mg/3 ml is rapidly and readily absorbed when administered orally, intravenously, or intramuscularly. Intestinal absorption is higher when it is injected intravenously compared to the intramuscular route.
Dormitol IM/IV Injection 15 mg/3 ml is rapidly metabolized in the liver by cytochrome P450 enzymes and subsequently excreted by the kidneys in the form of metabolites.
The dosage of midazolam is variable and depends on the patient's age, size, indication, route, and desired effects. When administered orally, typical adult dosages range from 0.5 mg to 6 mg taken two to three times daily. Intramuscular and Intravenous dosing typically ranges from 0.25 mg to 5 mg depending on the desired effect.
Dormitol IM/IV Injection 15 mg/3 ml can be administered orally, intramuscularly, and intravenously. Oral administration can be done with or without food. Intramuscular injection should be done in a deep muscle site with sterile technique.
Overdose of midazolam can be lethal as it can cause respiratory depression, hypotension, coma, and death. The risk of toxicity increases in cases of existing liver or kidney impairment, polymedication, and when other drugs are taken in conjunction with midazolam.
Dormitol IM/IV Injection 15 mg/3 ml interacts with many other drugs and can cause additive CNS depressant effects. Drugs such as opioids, benzodiazepines, antifungals, antipsychotics, calcium channel blockers, and certain antivirals may increase the sedative effects of midazolam. When combined with antiepileptic drugs (AEDs) or other drugs that affect liver enzyme activity, monitoring is recommended.
Dormitol IM/IV Injection 15 mg/3 ml does not interact with food, but it may take longer to take effect if taken with food.
Dormitol IM/IV Injection 15 mg/3 ml should not be taken by pregnant women due to the risk of teratogenic effects. Its safety has not been established for lactation. It should be avoided in women who are breastfeeding.
Dormitol IM/IV Injection 15 mg/3 ml should not be taken by lactating women due to the risk of teratogenic effects. Its safety has not been established for lactation. It should be avoided in women who are breastfeeding.
Acute overdose of midazolam increases the risk of coma, respiratory depression, hypotension, and death. Supportive measures and symptomatic treatment should be initiated promptly. Forced diuresis, dialysis, exchange transfusion, and hemodialysis are not expected to be effective in removing the drug from the body.
Dormitol IM/IV Injection 15 mg/3 ml should be stored in a tight container, away from heat, light, and humidity. Store at room temperature (15°C - 30°C).
The volume of distribution of midazolam is approximately 2.2 L/kg.
The half-life of midazolam is approximately 1.5 to 4.5 hours.
The mean clearance of midazolam is approximately 12 mL/min./kg.
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