Butamirate citrate is a centrally acting antitussive (cough suppressant) used to treat non-productive coughs. It is often prescribed when a cough is persistent and interferes with sleep or daily activities. Butamirate citrate is known for its non-narcotic nature, making it a preferable option over traditional opioid-based cough suppressants.
Butamirate citrate is used primarily for:
| Brand Name | Bulex |
|---|---|
| Type | Syrup |
| Weight | 7.5 mg/5 ml |
| Generic | Butamirate Citrate |
| Manufacturer | Everest Pharmaceuticals Ltd. |
| Available in | English বাংলা |
Butamirate citrate works by suppressing the cough reflex through central action on the medullary cough center in the brain. It reduces the frequency and intensity of coughing without causing sedation or affecting respiratory function significantly, which is common with narcotic cough suppressants.
The onset of action for butamirate citrate typically occurs within 30 to 60 minutes after oral administration. The duration of effect can vary but usually lasts for several hours, providing relief from coughing during this period.
Butamirate citrate is well absorbed from the gastrointestinal tract following oral administration. Peak plasma concentrations are generally achieved within 1 to 2 hours after ingestion.
Butamirate citrate is primarily metabolized in the liver. The drug and its metabolites are then excreted predominantly via the urine. The majority of the drug is eliminated through renal pathways.
The dosage of butamirate citrate varies depending on the formulation and the patient's age:
Butamirate citrate is administered orally in the form of tablets, capsules, or liquid solutions. It is important to follow the prescribed dosage and administration instructions provided by a healthcare provider.
Common side effects of butamirate citrate include:
Toxicity from butamirate citrate is rare but can occur if taken in excessive amounts. Symptoms of overdose may include severe drowsiness, nausea, vomiting, and gastrointestinal upset. In such cases, seek medical attention immediately.
Precautions include:
Butamirate citrate may interact with other medications, particularly:
Use with caution in individuals with:
Potential drug interactions include:
There are no specific food interactions with butamirate citrate. However, taking it with food may reduce gastrointestinal upset. It is advisable to follow the instructions provided by a healthcare provider regarding food intake.
Butamirate citrate is classified as a pregnancy Category C drug. It should only be used during pregnancy if the potential benefits outweigh the risks. Consult a healthcare provider for individualized advice.
The safety of butamirate citrate during lactation is not well-established. It is important to consult a healthcare provider before using this medication while breastfeeding to weigh potential risks and benefits.
Acute overdose of butamirate citrate may cause severe drowsiness, nausea, and vomiting. In cases of suspected overdose, seek medical attention immediately to manage symptoms and prevent complications.
Butamirate citrate is contraindicated in individuals with:
Follow the prescribed dosage and administration instructions carefully. Take butamirate citrate exactly as directed, and do not exceed the recommended dose. Consult a healthcare provider if symptoms persist or if there are any concerns regarding the medication.
Store butamirate citrate at room temperature, away from moisture and heat. Keep it in its original container and out of reach of children. Ensure the container is tightly closed to maintain efficacy.
The volume of distribution of butamirate citrate is not well-documented in the literature. However, it is distributed throughout the body after oral administration, with concentrations primarily in the tissues where cough reflex suppression occurs.
The half-life of butamirate citrate is approximately 6 to 8 hours. This duration can vary based on individual patient factors, including liver function and overall health.
Butamirate citrate is primarily cleared through renal excretion after liver metabolism. The rate of clearance can be affected by liver function and renal health, which may require dose adjustments in affected patients.
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