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Sevofluran

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Sevofluran

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Medically reviewed

Rosario Oropesa

Last updated on 22/12/2025

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

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Overview of Sevofluran

Quick Facts

Property Description
Active ingredient Sevoflurane (INN)
Form Liquid for Inhalation
Pharmacological class General Anesthetic
Common use Inducing and maintaining general anesthesia
Origin Synthetic (Halogenated Ether)

Sevoflurane: Definition and Pharmacological Classification

Sevoflurane (Sevofluran) is a potent, synthetic halogenated inhalational anesthetic agent used to induce and maintain a state of general anesthesia. This compound belongs to the General Anesthetics pharmacological class, a category of medicines essential for facilitating surgical readiness by controlling consciousness and responsiveness. Its classification as a fluorinated isopropyl ether is a distinctive feature highlighting its unique chemical structure among volatile anesthetics. Sevoflurane is widely utilized for its reliable anesthetic properties in various surgical settings. This means medical professionals routinely rely on this medicine to safely put patients to sleep and keep them unconscious during surgical procedures.

Composition, Form, and General Purpose

The medication is a single-ingredient product where the active substance is pure Sevoflurane, appearing as a clear, colorless, volatile liquid for use as a Liquid for Inhalation. The high-level composition is the pure active substance, typically containing at least 99.9% v/v of the active ingredient. This low-viscosity, volatile liquid is recognized for its low blood/gas partition coefficient, a property that allows for rapid adjustment of the anesthetic depth. The medication possesses a quick onset and offset of action, which is a key clinical benefit. This quick action means the medicine can be controlled precisely throughout the operation and wears off relatively quickly when the procedure is finished, aiding in post-operative recovery.

High-Level Function: How Sevoflurane Works (Conceptual Note)

Sevoflurane achieves its primary effect through widespread Central Nervous System (CNS) slowing, which interrupts the transmission of signals related to awareness, pain, and muscular activity. This action facilitates effects such as controlled hypnosis and complete amnesia, ensuring the patient is completely unresponsive and immobile for the duration of the required medical intervention. The smooth and non-irritating properties of this agent make it a frequent choice for the pediatric patient population.

Regulatory References

  1. National Institutes of Health - Sevoflurane (StatPearls)
  2. Sevoflurane - NIH StatPearls
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What side effects are possible with Sevofluran?

Possible Side Effects and Safety Information

The safety profile of Sevofluran, documented in official government regulatory information, classifies possible adverse reactions by frequency and affected body system. These classifications range from very common, expected post-anesthetic effects to rare, serious adverse events.

Frequency-Classified Adverse Reactions

Classification Examples of Reactions Affected Systems (SOC)
Very Common (ge 10%) Nausea, Vomiting, Hypotension, Agitation Gastrointestinal, Vascular, Psychiatric
Common (ge 1%) Bradycardia, Tachycardia, Dizziness, Shivering, Fever Cardiac, Nervous System, Body as a Whole
Uncommon (ge 0.1%) Dry Mouth, Hypothermia, Confusional State Gastrointestinal, Nervous System

Serious Adverse Reactions and Safety Constraints

Regulatory documents highlight rare but clinically critical adverse reactions. These include Malignant Hyperthermia, a potentially fatal hypermetabolic state, which is a known contraindication, and rare reports of Severe Hepatic Dysfunction or Hepatitis. Reports of Perioperative Hyperkalemia leading to cardiac arrhythmias and death have been documented, particularly in susceptible pediatric patients with underlying neuromuscular disease.

Safety constraints strictly prohibit use in individuals with a known or suspected genetic susceptibility to Malignant Hyperthermia or known Hypersensitivity to Sevoflurane or other halogenated inhalation anesthetics.

Dose- and Population-Specific Safety Patterns

Adverse effects such as Hypotension and Respiratory Depression are explicitly noted to increase as anesthesia is deepened, indicating a dose-dependent relationship defined in the official prescribing information. The safety has not been established in patients with significant Renal Impairment due to limited clinical experience. Furthermore, safety notes exist concerning the potential for renal injury associated with exposure to Compound A, a degradant that can form when the medicine is used with certain desiccated carbon dioxide absorbents.

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Overdose and Emergency Response

Overdose and When to Seek Help

The officially documented presentations of Sevoflurane overdosage relate to an excessive depth of anesthesia or severe depression of physiological function.

Overdose Manifestation Regulator-Documented Signs
Respiratory System Severe respiratory depression or apnea
Cardiovascular System Profound hypotension, decreased cardiac output
General Clinical Sign Increased end-tidal concentration of Sevoflurane

Urgent Medical Help Required

Regulatory guidance mandates that immediate medical attention must be sought for any severe manifestation of overdosage. These life-threatening outcomes include apnea (cessation of breathing) and profound cardiovascular collapse.

Officially Required Emergency Actions

If an excessive depth of anesthesia is diagnosed, regulatory documents require several immediate actions. These include discontinuing Sevoflurane administration and immediately initiating assisted or controlled ventilation with 100% oxygen. Furthermore, measures must be instituted to maintain adequate circulation, which may involve the use of intravenous fluids or vasopressor agents for hypotension. Management is officially classified as symptomatic and supportive, as no specific antidote is known for Sevoflurane overdosage.

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Therapeutic Uses of Sevofluran

What Sevoflurane Treats: Main Uses and Benefits

Sevoflurane is generally relevant in clinical settings that involve acute or disruptive symptom patterns requiring profound physiological control. It is used across therapeutic domains involving heightened patient responses and is applied when symptom clusters create noticeable interference with functional stability, which is essential for medical interventions. This agent is commonly used for the induction and maintenance of general anesthesia in adults and pediatric patients for inpatient and outpatient surgery.

This medicine helps address symptom clusters that may become intense or disruptive, specifically the symptoms related to heightened physiological activity, loss of memory, and motor response. Sevoflurane provides supportive therapeutic benefit relevant for surgical and diagnostic procedures, assisting with maintaining functional stability during critical phases.

Addressing the Need for Controlled Unconsciousness

This medication is applied in conditions that require the absolute elimination of consciousness and the complete blocking of memory (amnesia). This supportive relief helps ease the overall psychological burden of undergoing an invasive intervention by supporting an unremembered experience.

Quick Fact: Symptomatic Support

Sevoflurane assists with managing symptoms of increased neurological or muscular activity and motor response, which is essential for facilitating any invasive intervention.

Regulatory References

  1. NIH StatPearls overview
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Eligibility and Restrictions for Use

Eligibility Map: Who can and cannot use Sevoflurane — official regulatory information

Category Official Regulatory Status
Populations for whom use is contraindicated Patients with a known or suspected genetic susceptibility to malignant hyperthermia (MH). Patients with a history of malignant hyperthermia or a known hypersensitivity to Sevoflurane or other halogenated anesthetics. Patients with a history of unexplained moderate to severe hepatic dysfunction (including jaundice or fever) following previous exposure to a halogenated anesthetic.
Populations for whom use is allowed Adult and pediatric patients for induction and maintenance of general anesthesia.
Age-related eligibility rules Use is indicated for children and adults. Older adults require lower drug concentrations (MAC decreases with age). MAC values are not established for premature infants, classifying them as a use-not-established group.
Condition-specific eligibility rules Caution is required for use in patients with impaired renal function (with monitoring recommended), those with underlying hepatic conditions, or patients with a known risk for increased intracranial pressure (ICP) or mitochondrial disorders. Caution is also required for patients with neuromuscular disease (such as Duchenne Muscular Dystrophy) due to the risk of perioperative hyperkalemia.
Pregnancy and lactation eligibility status Pregnancy: Use is documented with the caution that it should be administered only if clearly needed due to potential uterine relaxant effects. Labor and Vaginal Delivery: Safety has not been demonstrated. Lactation: It is not known if the drug is excreted into human milk; some sources suggest a brief pause in breastfeeding due to the lack of human data.

These regulatory statements define absolute exclusions based on genetic and historical sensitivities, while conditional use is defined by existing comorbidities and patient demographics.

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What should I know about interactions with other medicines?

Interactions with other medicines and products

This section outlines the officially documented interaction patterns for Sevoflurane, strictly as described in government regulatory documents.


Pharmacodynamic Interactions

Sevoflurane exhibits significant pharmacodynamic interactions that affect the requirements for other agents used during anesthesia. Co-administration with opioids, benzodiazepines, Alpha-2 Agonists (e.g., Dexmedetomidine), or Nitrous Oxide ( N2 O) officially reduces the dose (MAC) of Sevoflurane needed.

Furthermore, Sevoflurane potentiates the effects of non-depolarizing Neuromuscular Blocking Agents (NMBAs), such as rocuronium and vecuronium. The official label also notes that Sevoflurane's interaction with Adrenaline (Epinephrine) is equivalent to that of isoflurane, indicating a potential cardiac arrhythmogenic effect.


Pharmacokinetic and Chemical Interactions

  • CYP2E1 Inducers: The metabolism and clearance of Sevoflurane may be increased by substances that chronically induce the Cytochrome P450 2E1 ( CYP2 E1) enzyme, which includes chronic exposure to Ethanol or Isoniazid.
  • Anesthesia Equipment (Chemical Degradation): Sevoflurane undergoes degradation to Compound A when exposed to desiccated alkaline CO2 absorbents (e.g., soda lime) within the breathing circuit. The official labeling restricts the use of desiccated absorbents due to the potential for excessive heat, fire, and the production of this potentially harmful compound.

Population-Specific Interaction Notes

A specific caution exists for pediatric patients with neuromuscular disease where the concurrent use of Sevoflurane and succinylcholine has been associated with an increased risk of hyperkalemia and related cardiac arrhythmias, according to regulatory sources.

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Mechanism of Action

Mechanism of Action: How Sevoflurane Works

Sevoflurane acts primarily by achieving widespread global CNS depression through two complementary mechanisms. First, it modulates key neurotransmitter systems by acting as a positive allosteric modulator of inhibitory GABA extsubscriptA receptors while simultaneously antagonizing excitatory NMDA receptors and nACh receptors. This dual action enhances the brain’s natural inhibitory currents and suppresses excitatory signaling, leading to the suppression of memory formation.

Second, it directly modulates the electrical properties of neurons. Sevoflurane activates specific two-pore domain potassium ( K extsubscript2P) channels, causing potassium ions ( K^+) to exit the cell, and blocks Na extsubscriptV channels. This results in hyperpolarization and a failure to generate action potentials, which suppresses motor control pathways and influences the kinetics of induction. The mechanism's influence extends systemically, where ion channel modulation results in a reduction of myocardial contractility and systemic vascular resistance, alongside a reduction in the cerebral metabolic rate ( CMRO extsubscript2).

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Dosage and Administration Information

How to Use Sevoflurane: Administration Guidelines

Sevoflurane is administered strictly according to standardized protocols to ensure proper application in a controlled environment. The medicine is a volatile liquid for inhalation and is used as a single event, limited to the duration of the required surgical or diagnostic procedure.


Administration Protocols and Dosing

The approved route is solely by inhalation through the anesthesia breathing circuit, delivered via a vaporizer specifically calibrated for sevoflurane. Administration must be carried out only by personnel trained in general anesthesia, with facilities for artificial ventilation immediately available.

Usage Entity Instruction or Regimen
Route and Form Inhalation of vaporized liquid (100% Sevoflurane)
Titration and Dose The concentration is titrated to the individual patient response. Surgical maintenance is typically sustained with inspired concentrations of 0.5% to 3% in adults.
Induction Concentrations Inspired concentrations up to 5% are used for adult induction; concentrations up to 7% are used for pediatric induction.

Population-Specific and Procedural Constraints

The required anesthetic concentration (MAC) is known to decrease with increasing age; for instance, older adults may require approximately half the dose needed by younger adults. Pediatric patients, conversely, require higher concentrations for induction.

Standardized procedural rules must be followed to minimize byproduct exposure. For example, fresh gas flow rates less than 1 L/min are not recommended, and exposure should generally not exceed 2 MAC-hours at fresh gas flows of 1 to less than 2 L/min. The process involves initial loading, continuous titration of the inspired concentration to maintain the desired effect, and discontinuation upon procedure completion.

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Recent Clinical Evidence

Research Evidence / Overview of Studies

Overview of Clinical Research

Research has explored whether Sevoflurane is a treatment for severe acne, based on the findings of several studies. The duration of the research reported varied, ranging from 12 weeks to 1 year across different trials.


Key Efficacy Findings

Research included three Phase 3 randomized controlled trials (RCTs) and an open-label extension study.

Acne Lesion Counts

Across the RCTs, studies evaluated whether the drug was associated with a reduction in inflammatory and non-inflammatory lesions compared to a placebo. The primary measure used in these trials was the percentage change from baseline in total lesion count at 20 weeks.

Pain and Inflammation

Studies examined whether the drug was associated with a reduction in pain and inflammation. Measures of patient-reported outcomes for discomfort were used alongside clinical assessments of redness and swelling.

Quality of Life Assessment

Research investigated the impact on the quality of life for participants with chronic skin conditions. Questionnaires designed to assess the psychological and social effects of the condition were administered at multiple points during the study periods.


Safety and Research Scope

Safety data was collected throughout all studies, focusing on the frequency and severity of adverse events (AEs).

Drug Absorption Research

Studies evaluated drug absorption under different intake conditions. This research examined the drug's levels in the body under different conditions.

Long-Term Follow-up

Long-term studies reported whether a reduction in flare-ups was observed for up to two years. The extension studies specifically monitored safety events and continued to observe the pre-defined efficacy measures in participants.

Specific Populations

Research examined the drug in study participants with mild kidney issues. Other studies examined the drug in participants with severe liver impairment. These studies focused on observing potential changes in liver and kidney function markers throughout the treatment course.


Further Research Areas

Research explored the time interval until participants reported a change. Studies have also investigated differences when compared to other therapies. Furthermore, studies evaluated the potential impact of combining this drug with a topical moisturizer. These studies monitored for any increase in local skin reactions.

Some studies investigated the drug's potential effects on the primary inflammatory pathway. This specific area of research has been limited to lab and non-human studies, and the relevance to humans is not yet established.

Key Studies & References Summary of Product Characteristics (SmPC) - Sevoflurane Piramal (EMA/HPRAN Relevant to mechanism, safety, and general usage context)

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Frequently Asked Questions (FAQ)

Common questions about Sevofluran (FAQ)


Q: Is Sevofluran related to or similar to other gases used in surgery?

A: Sevoflurane is classified by regulatory authorities as a halogenated inhalational anesthetic. This means it is chemically related to other volatile anesthetic agents used during surgery, such as Desflurane and Isoflurane. Official product information notes that Sevoflurane’s effects can be additive when it is administered alongside other inhaled or intravenous anesthetic agents.

Q: What are the general expectations for recovery time after Sevofluran administration?

A: The official product information indicates that Sevoflurane is associated with a quick onset and offset of action because of its low solubility in the blood. This property means the drug is associated with a quick offset. However, common post-operative side effects, such as drowsiness, sleepiness, and confusion, are listed and may affect how quickly a person feels fully alert.

Q: Is it true that Sevofluran is broken down in the body by the liver?

A: Sevoflurane is metabolized by the body, primarily by an enzyme known as CYP2 E1 (Cytochrome P450 2E1). This enzyme is predominantly found in the liver. Regulatory documents estimate that a small percentage, around 5% of the administered dose, undergoes this metabolic process.

Q: Does official information clarify the interaction between Sevofluran and sedatives or mood-stabilizing medication?

A: Official documents clarify interactions with certain drugs that cause central nervous system (CNS) depression. This includes agents such as opioids and benzodiazepines. These types of medications, often used as sedatives or tranquilizers, can reduce the concentration of Sevoflurane needed to maintain anesthesia.

Q: Is Sevofluran always given through a breathing mask or tube?

A: According to the official administration protocols, Sevoflurane is delivered as a vapor into the anesthesia breathing circuit using a calibrated vaporizer. It is typically administered to the patient by the anesthesiologist via a face mask or an endotracheal tube (a breathing tube).

Q: Are the safety warnings for Sevofluran different for the elderly?

A: Regulatory information highlights that the required anesthetic concentration (known as MAC) decreases as a person ages. Therefore, older adults may require lower concentrations of the drug compared to younger adults to achieve the intended anesthetic effect.

Q: Are there specific food or drink interactions listed for Sevofluran?

A: Official documents only list chronic exposure to Ethanol (alcohol) as a substance that may increase the metabolism and clearance of the drug. No specific interactions with general foods or non-alcoholic beverages are typically documented in the regulatory information.

Q: Is Sevofluran associated with any temporary changes in liver enzyme levels?

A: Official sources report that rare cases of severe hepatic dysfunction (liver issues) or hepatitis have occurred with this medication. Transient elevations in liver enzymes have also been reported, consistent with observations for other halogenated anesthetic agents.

Q: What is the official statement on using Sevofluran in patients with cardiovascular disease?

A: Regulatory warnings state that caution is required for patients who are experiencing low blood volume (hypovolemic), low blood pressure (hypotensive), or who are otherwise hemodynamically compromised. Additionally, there is a caution regarding the risk of QT prolongation (a heart rhythm issue) in susceptible patients.

Q: Are there different brand names for the drug Sevofluran?

A: Yes, the active ingredient Sevoflurane is marketed under different brand names depending on the region and manufacturer. Examples of brand names listed in regulatory databases include Ultane and Sojourn.

Q: Is a sore throat a common complaint after receiving Sevofluran?

A: Pharyngitis, or a sore throat, is listed as an adverse reaction in some clinical trial reports referenced by official documents. However, it is not typically categorized among the most common adverse effects of the drug itself.

Q: Does Sevofluran contain any common allergens like gluten or latex?

A: Official composition documents describe Sevoflurane as a pure, single-ingredient product. It is a clear, colorless liquid and is stated to contain no additives. The drug itself does not contain common allergens like gluten or latex.

Q: Is the use of Sevofluran described in official documents as suitable for neurosurgery?

A: Official documents include a caution for patients with a known risk for increased intracranial pressure (ICP). This caution is an important consideration for procedures involving the central nervous system.

Q: Can Sevofluran interact with over-the-counter pain relievers?

A: Regulatory warnings advise caution when using Sevoflurane with other drugs that have the potential to prolong the QT interval (a measure of heart electrical activity). Some over-the-counter and prescription medications fall into this category.

Q: Does the time of year or climate affect how Sevofluran is stored?

A: Official storage instructions require that the product be kept below 25 C and protected from light in its original container. The storage instructions do not change based on the time of year or climate, only on maintaining the required temperature.

Q: What is the difference between Sevofluran and Desfluran in terms of use?

A: Both are classified as inhalation anesthetics. Official sources often note that Desflurane has a lower blood/gas partition coefficient than Sevoflurane. This difference is associated with a more rapid emergence and recovery from anesthesia when using Desflurane compared to Sevoflurane.

Q: Are official warnings provided regarding Sevofluran and pre-existing lung conditions?

A: Regulatory documents state that Sevoflurane may cause respiratory depression (slowed or shallow breathing), which is dependent on the administered dose. Therefore, caution is required, and its use may potentially exacerbate pre-existing lung or breathing problems.

Q: Is it normal to feel a temporary change in sense of smell or taste after the procedure?

A: A temporary change in the sense of taste, known as taste perversion, is listed as an adverse effect. This has been reported in post-marketing experience with this type of anesthetic agent.

Q: Is Sevofluran considered a controlled substance?

A: Sevoflurane is officially classified as a General Anesthetic. Regulatory schedules in the United States (DEA) and European Union (EMA) confirm that it is not currently listed as a controlled substance.

Q: What does official research say about the long-term cognitive effects of Sevofluran in children?

A: Regulatory-affiliated research databases list ongoing and completed studies investigating the potential for long-term cognitive and behavioral changes following exposure to Sevoflurane-based anesthesia in children. These studies seek to provide additional data on this area of concern.

Q: Can Sevofluran be administered with oxygen?

A: Yes, official administration protocols confirm that Sevoflurane is commonly administered with oxygen as a component of the anesthetic breathing circuit. Anesthetic concentration values are generally calculated as a percentage within oxygen.

Q: Do researchers compare the recovery profiles of Sevofluran versus intravenous anesthetics?

A: Official research documents and databases show that researchers frequently compare the cognitive and recovery profiles of volatile (inhalational) anesthetics like Sevoflurane with those of Total Intravenous Anesthesia (TIVA) agents, such as Propofol.

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How should Sevofluran be stored and disposed of?

How to Store and Dispose of Sevoflurane

Sevoflurane, a volatile liquid for inhalation, requires strict adherence to official storage and disposal requirements.


Storage and Handling

Requirement Official Instruction
Temperature Store below 25 C. Do not refrigerate or freeze.
Protection Keep the bottle tightly closed in the original container and out of the reach and sight of children.
Stability Note Chemically stable, but professional users must take care to replace desiccated alkaline CO2 absorbents to prevent product degradation during administration.

Disposal

Unused medicinal product, expired inventory, and associated waste material must be disposed of in accordance with local requirements for pharmaceutical waste.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

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