SURVANTA 25MG INJECTION 8 ML
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SURVANTA 25MG INJECTION 8 ML
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SURVANTA 25MG INJECTION 8 ML

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SURVANTA 25MG INJECTION 8 ML

By ABBOTT HEALTH CARE PRIVATE LIMITED

MRP

17479.47

₹16605.5

5 % OFF

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About SURVANTA 25MG INJECTION 8 ML

  • Survanta 25mg Injection 8ml is a sterile, non-pyrogenic pulmonary surfactant intended for intratracheal use only. It is extracted from natural bovine lung extract supplemented with dipalmitoylphosphatidylcholine (DPPC), palmitic acid, tripalmitin, and proteins to closely mimic natural human surfactant. This composition helps to reduce surface tension in the lungs and improves oxygen exchange.
  • This medication is primarily used in the treatment and prevention of Respiratory Distress Syndrome (RDS) in premature infants. RDS occurs when a baby's lungs are not fully developed and do not produce enough surfactant on their own. By administering Survanta, the surface tension within the alveoli of the lungs is reduced, preventing alveolar collapse and promoting easier breathing.
  • The dosage and frequency of Survanta administration depend on the infant's weight and the severity of the RDS. It is administered intratracheally, directly into the baby's lungs through an endotracheal tube. Medical professionals carefully monitor the infant's respiratory status and adjust the treatment as needed.
  • It is crucial to use Survanta under strict medical supervision due to potential side effects like bradycardia, oxygen desaturation, and endotracheal tube blockage. Regular monitoring and prompt management of these side effects are vital to ensure the baby's safety and well-being. Survanta has significantly improved the survival rates and reduced complications associated with RDS, making it a vital component in neonatal intensive care.
  • Store Survanta in a refrigerator at 2-8°C (36-46°F). Do not freeze. Protect from light. Single-use vial, discard any unused portion.

Uses of SURVANTA 25MG INJECTION 8 ML

  • Treatment of Respiratory Distress Syndrome (RDS) in premature infants.
  • Prophylaxis of Respiratory Distress Syndrome (RDS) in premature infants at risk.
  • Improving lung function by reducing surface tension in the lungs.

How SURVANTA 25MG INJECTION 8 ML Works

  • SURVANTA (beractant) is a lung surfactant used to prevent and treat Respiratory Distress Syndrome (RDS) in premature infants. RDS occurs because premature babies often lack sufficient natural surfactant, a substance that helps the lungs inflate and exchange oxygen and carbon dioxide effectively. SURVANTA works by replenishing this missing surfactant, improving lung function and making it easier for the baby to breathe.
  • The active ingredient in SURVANTA, beractant, is a modified natural bovine (cow) lung extract. It contains phospholipids, neutral lipids, fatty acids, and surfactant-associated proteins SP-B and SP-C. These components work together to mimic the function of natural human surfactant. Phospholipids, particularly dipalmitoylphosphatidylcholine (DPPC), are the main surface-active components responsible for reducing surface tension in the alveoli (tiny air sacs in the lungs).
  • When SURVANTA is administered into the infant's lungs via an endotracheal tube, the phospholipids spread along the air-liquid interface of the alveoli. This reduces surface tension, preventing the alveoli from collapsing at the end of each breath. By stabilizing the alveoli, SURVANTA improves lung compliance, meaning the lungs become easier to inflate. This, in turn, reduces the work of breathing for the infant and improves gas exchange, leading to increased oxygen levels in the blood and decreased carbon dioxide levels.
  • The surfactant-associated proteins SP-B and SP-C play a crucial role in the proper functioning of SURVANTA. SP-B helps to spread the phospholipids rapidly across the alveolar surface and is essential for the formation of a stable surfactant film. SP-C also contributes to the spreading and stability of the surfactant layer. These proteins ensure that the surfactant effectively reduces surface tension throughout the lungs.
  • In essence, SURVANTA works by providing a replacement for the missing or deficient natural surfactant in premature infants with RDS. This replacement surfactant lines the alveoli, reduces surface tension, and stabilizes the air sacs, allowing the lungs to inflate properly and facilitating effective gas exchange. By improving lung function, SURVANTA significantly reduces the severity of RDS and improves the chances of survival and long-term health for premature infants.

Side Effects of SURVANTA 25MG INJECTION 8 MLArrow

While SURVANTA (beractant) Injection can be life-saving for premature infants with Respiratory Distress Syndrome (RDS), it's important to be aware of potential side effects. These can range from common to rare, and it's crucial to discuss any concerns with your doctor. **Common Side Effects (occurring in a significant number of patients):** * **Bradycardia (Slow Heart Rate):** A temporary slowing of the heart rate may occur during administration. * **Decreased Oxygen Saturation:** Oxygen levels in the blood may temporarily decrease. * **Endotracheal Tube Reflux:** The medication may back up into the endotracheal tube. * **Pallor (Paleness):** The infant's skin may appear paler than usual. * **Vasoconstriction:** Narrowing of blood vessels. **Less Common Side Effects (occurring in a smaller number of patients):** * **Apnea (Temporary Cessation of Breathing):** Breathing may stop for a short period. * **Pulmonary Hemorrhage:** Bleeding in the lungs. * **Mucus Plugging:** Blockage of the endotracheal tube with mucus. **Rare Side Effects (occurring very rarely):** * **Infection:** Introduction of infection. * **Post-treatment complications:** Complications arising after the treatment of this medicine **Important Considerations:** * This is not an exhaustive list, and other side effects may occur. * The healthcare team will closely monitor the infant for any adverse reactions during and after SURVANTA administration. * Report any unusual signs or symptoms to the medical staff immediately. * The benefits of SURVANTA in treating RDS usually outweigh the potential risks of side effects. **Tags:** SURVANTA, beractant, side effects, Respiratory Distress Syndrome, RDS, premature infants, bradycardia, apnea, pulmonary hemorrhage, mucus plugging, decreased oxygen saturation, endotracheal tube reflux, pallor, vasoconstriction, infection, post-treatment complications

Safety Advice for SURVANTA 25MG INJECTION 8 MLArrow

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Allergies

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Consult your doctor if you are allergic to it.

Dosage of SURVANTA 25MG INJECTION 8 MLArrow

  • The recommended dosage of SURVANTA (beractant) 25mg/mL injection is 4 mL/kg birth weight. This initial dose should be administered as soon as possible, preferably within 15 minutes of birth, for infants with Respiratory Distress Syndrome (RDS).
  • Subsequent doses of 4 mL/kg birth weight can be given, up to a total of four doses within the first 48 hours of life. These repeat doses should be administered if the infant remains on a ventilator and shows evidence of persistent RDS.
  • The interval between doses should be at least 6 hours. Dosage should be based on the infant's birth weight, and accurate measurement is crucial. The injection should be administered intratracheally, divided into quarter doses. Position the infant differently after each quarter dose to maximize distribution within the lungs. Monitor the infant closely for signs of oxygen desaturation, bradycardia, and airway obstruction during and after administration.
  • If adverse reactions occur, stop the administration and take appropriate measures to stabilize the infant. Before administering SURVANTA, ensure proper placement of the endotracheal tube. Suction the infant prior to administration only if clinically necessary. After each dose, avoid suctioning for at least one hour unless signs of significant airway obstruction are present. Remember that proper monitoring and supportive care are essential components of successful SURVANTA therapy.
  • Take 'SURVANTA 25MG INJECTION 8 ML' only as per the prescription by your physician only.

What if I miss my dose of SURVANTA 25MG INJECTION 8 ML?Arrow

  • SURVANTA is administered in a neonatal intensive care unit (NICU) setting by trained medical professionals. Since the medication is crucial for premature infants with respiratory distress syndrome, a missed dose is unlikely as the dosing schedule is closely monitored. If a dose is inadvertently missed, the medical team will assess the infant's condition and administer the dose as soon as possible, guided by established medical protocols and the infant's clinical needs.

How to store SURVANTA 25MG INJECTION 8 ML?Arrow

  • Keep SURVANTA 25MG INJ 8ML away from the reach of children and pets.
  • Store SURVANTA 25MG INJ 8ML in a refrigerator (2 - 8°C). Do not freeze.

Benefits of SURVANTA 25MG INJECTION 8 MLArrow

  • SURVANTA 25MG INJECTION 8 ML offers a multitude of benefits for premature infants at risk of, or suffering from, Respiratory Distress Syndrome (RDS). Its primary function is to reduce surface tension in the lungs, a critical factor in enabling proper breathing. By administering SURVANTA, clinicians can significantly improve lung function and overall respiratory performance in these vulnerable newborns.
  • The administration of SURVANTA leads to a marked decrease in the severity of RDS. This translates to less labored breathing, improved oxygenation, and a reduced need for mechanical ventilation. By stabilizing the alveoli, the tiny air sacs in the lungs, SURVANTA allows for more efficient gas exchange, ensuring that the infant's body receives the oxygen it needs to thrive.
  • A key advantage of SURVANTA is its ability to minimize the duration of mechanical ventilation. Prolonged ventilation can lead to lung injury and other complications. By improving lung function rapidly, SURVANTA reduces the infant's reliance on ventilators, thereby lowering the risk of ventilator-associated problems such as bronchopulmonary dysplasia (BPD), a chronic lung disease common in premature infants.
  • SURVANTA contributes to improved oxygenation levels in premature infants with RDS. By facilitating better gas exchange, it helps maintain optimal blood oxygen saturation, which is crucial for brain development and overall organ function. This, in turn, reduces the risk of hypoxia-related complications.
  • By mitigating the severity of RDS and promoting improved lung function, SURVANTA can significantly lower the risk of mortality associated with prematurity and respiratory complications. Studies have shown that early administration of SURVANTA improves survival rates among premature infants with RDS.
  • Beyond its immediate effects on lung function, SURVANTA also plays a role in reducing the incidence of long-term respiratory complications. By preventing lung damage from prolonged ventilation and improving overall lung development, it can lower the risk of chronic lung diseases such as BPD, leading to healthier outcomes later in life.
  • SURVANTA's effectiveness allows for a potential reduction in the need for supplemental oxygen therapy. This decreases the risk of oxygen toxicity and other potential complications associated with prolonged oxygen exposure. Achieving stable oxygen saturation levels more quickly is a significant benefit.
  • Clinical trials and extensive use in neonatal intensive care units have established a strong safety profile for SURVANTA. While all medications carry some risk, SURVANTA has been shown to be generally well-tolerated by premature infants. Monitoring is essential, but serious adverse reactions are relatively uncommon.
  • The use of SURVANTA can translate to shorter stays in the Neonatal Intensive Care Unit (NICU). By improving respiratory function and reducing the need for intensive interventions, it can facilitate earlier discharge, allowing infants to return home with their families sooner. This also reduces healthcare costs.
  • Overall, SURVANTA 25MG INJECTION 8 ML is an essential tool in the management of RDS in premature infants, offering a comprehensive range of benefits from improved lung function and reduced reliance on ventilation to decreased mortality and a lower risk of long-term respiratory complications. Its proven efficacy and safety profile make it a cornerstone of neonatal care for premature infants at risk of, or suffering from, RDS.

How to use SURVANTA 25MG INJECTION 8 MLArrow

  • SURVANTA (beractant) Intratracheal Suspension is administered intratracheally. It is crucial that SURVANTA be administered by trained medical professionals experienced in neonatal resuscitation and respiratory management. Before administering SURVANTA, ensure proper placement of the endotracheal tube.
  • The recommended dose of SURVANTA is 4 mL/kg birth weight. Up to four doses can be administered in the first 48 hours of life. Doses should be given no more frequently than every 6 hours. The first dose should be administered as soon as possible, ideally within 15 minutes of birth, for infants with documented Respiratory Distress Syndrome (RDS).
  • To administer, warm SURVANTA by holding the vial in your hand for at least 20 minutes or warming in an incubator. DO NOT use artificial warming methods. Swirl the vial gently to re-suspend. DO NOT shake. Withdraw the entire contents of the vial into a syringe. Attach the pre-cut 5 French feeding tube to the syringe.
  • Position the infant appropriately. Divide the dose into four equal portions. Administer each portion slowly over 2-3 minutes. After each portion, remove the feeding tube and manually ventilate the infant with oxygen for at least 30 seconds or until stable. The recommended positions are: Dose 1 - head turned to the right; Dose 2 - head turned to the left; Dose 3 - head turned to the right; Dose 4 - head turned to the left.
  • After the completion of the dosing procedure, monitor the infant closely for signs of airway obstruction, bradycardia, or desaturation. Suction only if absolutely necessary to avoid surfactant removal. Adjust ventilator settings as needed to maintain adequate oxygenation and ventilation.

Quick Tips for SURVANTA 25MG INJECTION 8 MLArrow

  • **Understanding Surfactant Replacement Therapy:** SURVANTA® is a lung surfactant used to treat and prevent Respiratory Distress Syndrome (RDS) in premature infants. It helps reduce surface tension in the lungs, allowing them to inflate more easily.
  • **Dosage and Administration:** SURVANTA® is administered intratracheally (directly into the trachea/windpipe). Dosage is based on the infant's birth weight and is typically given in multiple doses. Administration should only be performed by trained medical personnel.
  • **Monitoring During Administration:** Closely monitor the infant's heart rate, blood pressure, and oxygen saturation during and after SURVANTA® administration. Temporary changes in these vital signs are common, and medical staff are prepared to manage them.
  • **Potential Side Effects:** While SURVANTA® is generally safe, potential side effects can include bradycardia (slow heart rate), decreased oxygen saturation, and airway obstruction. The medical team is equipped to handle these events promptly.
  • **Storage and Handling:** SURVANTA® requires refrigeration. Before administration, it should be warmed slowly to room temperature, avoiding rapid heating methods. Unopened vials should be protected from light.
  • **Importance of Supportive Care:** SURVANTA® is most effective when combined with other supportive measures, such as mechanical ventilation and oxygen therapy. These therapies help stabilize the infant's condition and optimize the benefits of surfactant replacement.
  • **Educating Parents:** Although the administration is done by medical professionals, parents should be informed about RDS, SURVANTA®, and the expected course of treatment. Understanding the process can help alleviate anxiety and promote informed decision-making.
  • **Avoid Shaking the Vial:** Gently swirl the vial to ensure the medication is uniformly dispersed. Avoid vigorous shaking, as this can damage the surfactant lipids.
  • **Multiple Doses May Be Necessary:** Depending on the infant's response, repeat doses of SURVANTA® may be required. The medical team will assess the infant's condition and determine the need for additional doses.
  • **Documenting the Procedure:** Meticulous documentation of the administration process, including dosage, vital signs, and any adverse events, is crucial for tracking the infant's progress and ensuring optimal care.

Food Interactions with SURVANTA 25MG INJECTION 8 MLArrow

  • SURVANTA 25MG INJECTION 8 ML is administered directly into the lungs of premature infants by medical professionals. As such, it does not interact with food. It is crucial to follow the medical professional’s guidance regarding infant feeding schedules.

FAQs

What is SURVANTA Injection and what is it used for?

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SURVANTA Injection is a lung surfactant used to treat Respiratory Distress Syndrome (RDS) in premature infants. It helps the lungs to function properly.

How is SURVANTA Injection administered?

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SURVANTA Injection is administered directly into the infant's windpipe (trachea) by a trained medical professional.

What are the common side effects of SURVANTA Injection?

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Common side effects of SURVANTA Injection include temporary decrease in oxygen saturation, bradycardia (slow heart rate), and airway obstruction.

What is the dosage of SURVANTA Injection?

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The dosage of SURVANTA Injection depends on the infant's weight. Typically, it is administered as 100 mg of phospholipid per kilogram of body weight.

Are there any contraindications for SURVANTA Injection?

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There are no known absolute contraindications for SURVANTA Injection, but it should be used with caution if the infant has a known hypersensitivity.

How should SURVANTA Injection be stored?

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SURVANTA Injection should be stored in a refrigerator between 2-8 degrees Celsius (36-46 degrees Fahrenheit). Do not freeze it.

Can SURVANTA Injection interact with other medications?

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Significant drug interactions with SURVANTA Injection are not known, but always inform the healthcare provider about all medications to avoid any potential risks.

What are the symptoms of an overdose of SURVANTA Injection?

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Symptoms of an overdose of SURVANTA Injection may include fluid build-up in the lungs, decreased oxygen levels, and difficulty breathing.

How quickly does SURVANTA Injection start working?

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Improvement in lung function is typically seen within a few hours after SURVANTA Injection is administered.

Can SURVANTA Injection completely cure RDS?

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SURVANTA Injection helps to reduce the symptoms of RDS and improve lung function, but it may not completely cure the underlying condition.

What are the alternatives if SURVANTA Injection is not available?

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Alternatives to SURVANTA Injection include other lung surfactants, and supportive care, such as mechanical ventilation, will still be provided.

What is the price of SURVANTA Injection?

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The price of SURVANTA Injection can vary depending on the region and supplier. Please contact your local pharmacy or healthcare provider for specific pricing information.

Can SURVANTA Injection be used in adults?

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SURVANTA Injection is primarily intended for premature infants and its use in adults has not been studied.

When might repeat doses of SURVANTA Injection be needed?

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If the infant does not show improvement in RDS symptoms after the initial dose, additional doses may be needed to improve lung function.

Are there any long-term risks associated with the use of SURVANTA Injection?

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There are no known significant long-term risks associated with the use of SURVANTA Injection. However, it is important to discuss any potential risks with healthcare providers.

References

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SURVANTA (beractant) Intratracheal Suspension. US Prescribing Information. Initial U.S. Approval: 1991.

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SURVANTA - beractant suspension. DailyMed. Current revision date: 27 July 2023

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Fujiwara T, Chida S, Watabe Y, Maeta H, Morita T, Abe T. Artificial surfactant therapy in hyaline-membrane disease. Lancet. 1980 Jan 5;1(8159):55-9.

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Speer CP. Surfactant replacement therapy: past, present and future. Early Hum Dev. 2009 Aug;85(8):405-14. doi: 10.1016/j.earlhumdev.2009.02.004. Epub 2009 Mar 12.

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UpToDate - Surfactant replacement therapy in the neonate

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SURVANTA 25 mg/ml intratracheal suspension - Summary of Product Characteristics (SmPC)

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SURVANTA 25MG INJECTION 8 ML

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