Xylocard

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Medically reviewed

Marina Burgos

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.

Overview of Xylocard

Property Description
Active ingredient Lidocaine Hydrochloride (Lidocaine, Lignocaine)
Form Sterile Aqueous Solution for Injection
Pharmacological class Antiarrhythmic Agent (Class IB)
Route Intravenous (Parenteral)
Origin Synthetic Compound

Identity: What Kind of Medication is Xylocard?

Xylocard is a synthetic, prescription-only medication that is formally categorized as an Antiarrhythmic Agent, specifically developed for cardiac stabilization. Its active component, Lidocaine Hydrochloride, is a compound whose membrane-stabilizing properties have been clinically recognized for decades in critical care settings. This agent is classified as a Group I antiarrhythmic, placing it in a specialized class intended to address certain unstable and erratic heart rhythms. The compound itself is recognized globally for its therapeutic importance and is included on the World Health Organization's List of Essential Medicines.

Composition and Form: The Specialized Intravenous Solution

The medicine is supplied as a single-ingredient product, a sterile aqueous solution for injection intended exclusively for parenteral administration via the intravenous route. This preparation, which is a synthetic compound, bypasses the digestive system entirely. The specialized liquid form is essential to ensure the rapid onset of action required for immediate intervention during acute cardiac electrical disturbances. Unlike oral or topical forms of Lidocaine, this formulation is meticulously manufactured for the critical demands of systemic delivery.

General Purpose: Restoring Electrical Stability

The fundamental purpose of this medication is to help restore the heart to a stable and regular rhythm in specific, acute scenarios. It achieves this by acting as a Voltage-gated sodium channel blocker. This action regulates the flow of ions, which reduces the excitability of heart muscle cells. This effect helps to control chaotic electrical impulses, supporting the heart in re-establishing coordinated and effective beating.

Regulatory References

  1. World Health Organization's List of Essential Medicines

What side effects are possible with Xylocard?

Possible side effects and safety information

The safety profile for intravenous Lidocaine Hydrochloride (Xylocard) is principally characterized by dose-related systemic toxicity, with adverse reactions generally proportional to the concentration of the drug in the blood plasma.

Adverse Reaction Scope

The most commonly classified adverse reactions involve the Central Nervous System (CNS) and the Cardiovascular System. Early CNS manifestations may include light-headedness, dizziness, drowsiness, apprehension, and tinnitus. More severe CNS effects, often related to higher systemic levels, include muscular twitching, tremors, and convulsions. Cardiovascular effects include a reduction in blood pressure (hypotension) and heart rate (bradycardia).

Serious adverse reactions officially documented in regulatory labels include Cardiovascular Arrest, Respiratory Arrest, and Convulsions. Allergic reactions, including anaphylaxis, are also documented, typically classified as infrequent events [FDA Product Labeling].

Safety Considerations and Restrictions

Regulatory documents highlight that the medicine is contraindicated for patients with specific pre-existing heart rhythm conditions, such as Stokes-Adams syndrome or severe degrees of heart block (in the absence of an artificial pacemaker). The risk of adverse effects is officially linked to plasma concentration, with objective adverse signs becoming apparent above a defined toxicity threshold.

Specific caution and potential dosage adjustment are officially required for older adults and individuals with severe hepatic or renal impairment. This is due to the potential for reduced clearance, which can lead to drug accumulation, particularly during prolonged infusions.

This regulatory structure defines the medicine's risk profile by establishing clear constraints on use and identifying the major organ systems where adverse events are classified.

Overdose and Emergency Response

Overdose and When to Seek Help

This section outlines the officially documented manifestations and required actions in case of an overdose of Xylocard (Lidocaine Hydrochloride), based on authoritative government regulatory documents.

Documented Overdose Manifestations

Overdose or systemic toxicity primarily affects the Central Nervous System (CNS) and the Cardiovascular System (CVS) due to excessively high plasma concentrations.

System Early Warning Signs Severe Manifestations
CNS Lightheadedness, confusion, dizziness, tinnitus, tremors Convulsions (seizures), unconsciousness, respiratory arrest
CVS Bradycardia (slow heart rate), hypotension (low blood pressure) Cardiovascular collapse, cardiac arrest

Other documented effects include acidosis and methemoglobinemia. Delayed proper management of dose-related toxicity may lead to cardiac arrest and potentially death.

Required Emergency Action

Immediate medical attention must be sought if the patient shows any signs of systemic toxicity, such as lethargy, shallow breathing, or seizure activity. The infusion must be terminated at the earliest sign of toxicity. Regulatory documentation mandates that resuscitative equipment, including oxygen, must be immediately available for managing acute emergencies.

Population-Specific Notes

Reduced doses are officially required for children, the elderly, and acutely ill or debilitated patients. Patients with hepatic dysfunction may experience a significantly prolonged half-life, increasing the risk of toxicity.

Therapeutic Uses of Xylocard

What Xylocard Treats: Main Uses and Benefits

Intravenous Lidocaine Hydrochloride is considered relevant in the acute management of certain conditions, primarily those involving disruptive ventricular arrhythmias. This clinical relevance includes conditions associated with an acute myocardial infarction or those arising during cardiac manipulative procedures such as surgery.


Focus on Electrical Stabilization

Xylocard is generally applied in clinical settings that involve acute or unstable symptom patterns. It is used for managing symptom groups associated with heightened physiological activity and noticeable physiological strain, which include very rapid and disorganized heart rhythms. This application provides supportive relief that helps maintain a sense of stability when symptoms are more noticeable.

Its application is summarized by the idea:

“It is commonly applied in scenarios where additional management of discomfort is required, and assists with maintaining general well-being during symptomatic phases.”

Quick Fact: Support for Heightened Physiological Activity

This treatment is commonly used when symptoms intensify, providing assistance with managing rapid and disruptive contractions to help support a sense of stability during acute episodes.

Eligibility and Restrictions for Use

Xylocard (lidocaine hydrochloride injection) is a prescription medicine administered by healthcare professionals, typically in a hospital setting for the management of ventricular arrhythmias.

Contraindications (Who Cannot Use Xylocard)

Xylocard is generally contraindicated and should not be used in patients with:

  • Hypersensitivity: A known allergy to lidocaine or other local anesthetics of the amide type (e.g., bupivacaine, mepivacaine).
  • Severe Heart Block: Conditions such as Adams-Stokes syndrome, severe sinoatrial, atrioventricular (AV), or intraventricular block, especially in the absence of a pacemaker.
  • Wolff-Parkinson-White Syndrome.

Precautions (Use with Caution)

Caution and dosage adjustment are required when administering Xylocard to patients with certain medical conditions, as these factors can increase the risk of toxicity or adverse effects. These include:

  • Cardiovascular Issues: Congestive heart failure, severe low blood pressure (hypotension), or bradycardia (slow heart rate).
  • Organ Dysfunction: Impaired liver (hepatic) or kidney (renal) function, which can slow the body's clearance of the drug.
  • Other: The elderly, acutely ill or debilitated patients, and those with epilepsy or severe shock often require reduced doses and close monitoring.

What should I know about interactions with other medicines?

The active substance in Xylocard (lidocaine) is primarily metabolized in the liver by the enzymes CYP1A2 and CYP3A4. Interactions with other medicinal products largely stem from interference with this metabolic pathway or with the blood flow to the liver.

Medicines That May Increase Xylocard Levels

Certain medicines can increase the plasma concentration of Xylocard, raising the potential for dose-related side effects. Caution and close monitoring are required if Xylocard is administered with the following categories of medicines:

  • Beta-blockers (e.g., propranolol, metoprolol): These drugs may reduce the clearance of intravenous lidocaine, potentially by lowering hepatic blood flow and/or affecting liver metabolism. Coadministration with agents like propranolol has been reported to significantly increase lidocaine concentration.
  • Strong CYP1A2 Inhibitors: Medicines that strongly block the CYP1A2 enzyme, such as fluvoxamine, can reduce the breakdown and elimination of lidocaine, resulting in higher plasma levels.
  • Antiarrhythmics: Other medicines used to control heart rhythm, such as amiodarone, have non-specific inhibitory effects on CYP-mediated metabolism that may result in increased lidocaine plasma levels and potential toxicity.

Other Potential Interactions

  • CYP3A4 Inducers: Medicines that increase the activity of the CYP3A4 enzyme, such as phenytoin, carbamazepine, or phenobarbital, may slightly decrease lidocaine plasma levels, though a dose adjustment is typically not required.

Before receiving Xylocard, all healthcare providers must be informed of all medicines being taken, including prescription, over-the-counter, herbal, and supplement products.

Mechanism of Action

Sodium Channel Blockade (Class IB)

This core mechanism involves Xylocard (lidocaine) binding to and blocking voltage-gated sodium (Na^+) channels primarily in the ventricular myocardium. This action selectively inhibits the fast sodium ion influx during the depolarization phase (Phase 0) of the cardiac action potential, which reduces the frequency of rapid sodium ion influx in electrically unstable tissue. This binding exhibits use-dependence, favoring channels in rapidly firing or partially depolarized cells, thereby modifying the electrical conduction properties of the myocardium.


Electrophysiological Consequences

The binding kinetics of Xylocard lead to the suppression of automaticity in ectopic pacemaker cells within the His-Purkinje system and ventricles. This occurs by depressing the spontaneous depolarization rate (Phase 4), which decreases the likelihood of these cells achieving threshold potential and initiating subsequent electrical events. Furthermore, the mechanism induces a shortening of the action potential duration (APD) and the effective refractory period (ERP) in the ventricular muscle cells, facilitating rapid repolarization in cardiac myocytes and affecting the necessary conditions for re-entry to occur.

Dosage and Administration Information

How Xylocard is Used: Official Administration Guidelines

Xylocard (Lidocaine Hydrochloride Injection) is an antiarrhythmic agent whose administration is governed by a precise, two-phase intravenous protocol. This medication is exclusively for parenteral administration via the intravenous (IV) route and is restricted to healthcare settings where continuous ECG monitoring and resuscitative equipment are immediately available.

Dosing and Frequency

Therapy begins with an initial IV bolus of 50 to 100 mg (or 0.7 to 1.4 mg/kg), which must be administered slowly over a period of two to three minutes to mitigate adverse effects. If the acute condition persists, a secondary bolus of 25 to 50 mg may be given approximately five minutes after the first. Following the bolus, treatment immediately transitions to a continuous IV infusion at a rate typically ranging from 1 to 4 mg/minute to maintain stable drug levels. The maximum total dose should generally not exceed 300 mg within a one-hour period.

Preparation and Adjustments

For the continuous infusion, the concentrated solution requires dilution to achieve a final working concentration, such as 1 mg/mL (e.g., 1 gram in 1 liter of D5W). The administration of the infusion must be managed using a controlled pump to ensure accuracy. Dosage adjustments are mandatory for certain populations: a reduced dose is required for geriatric patients and those with established conditions like hepatic impairment (liver dysfunction) or congestive heart failure due to altered drug clearance. This regimen is intended for short-term, acute stabilization, not for long-term maintenance.

Recent Clinical Evidence

Xylocard (lidocaine hydrochloride) is a Class Ib antiarrhythmic agent historically used for the acute management of ventricular arrhythmias, such as ventricular tachycardia (VT) and ventricular fibrillation (VF), particularly in the context of myocardial ischemia or acute myocardial infarction (AMI).

Current Role in Resuscitation

Clinical guidelines now suggest that Xylocard may be considered an alternative to amiodarone for the treatment of shock-refractory VF/pulseless VT during advanced cardiac life support (ACLS) protocols. This indicates its continuing, though secondary, role in emergent settings.

  • Out-of-Hospital Cardiac Arrest (OHCA): Randomized trials comparing lidocaine, amiodarone, and placebo in patients with shock-refractory OHCA have generally not demonstrated a significant difference in the rates of survival to hospital discharge or favorable neurological outcomes. However, some evidence suggests both antiarrhythmics may contribute to a higher rate of return of spontaneous circulation (ROSC) compared to placebo.

Use in Myocardial Infarction and Prevention

Evidence has led to changes regarding its prophylactic use following a heart attack:

  • Prophylaxis in AMI: Routine prophylactic use of lidocaine in all patients with acute myocardial infarction is no longer widely recommended. While early studies showed that prophylactic administration may reduce the incidence of ventricular fibrillation, the overall impact on mortality rates was not consistently beneficial and, in some cases, was associated with an increased risk of asystole.

Contextual Efficacy

Research indicates Xylocard is generally most effective for ventricular arrhythmias of acute onset. Its use is typically reserved for hemodynamically stable monomorphic VT or for refractory VT/VF when other treatments are unavailable or contraindicated. The drug's narrow therapeutic window necessitates close clinical and electrocardiographic monitoring during administration.

Frequently Asked Questions (FAQ)

Common questions about Xylocard (FAQ)

Q: Is Xylocard the same drug as lidocaine?

A: Yes, Xylocard is a specific brand name for the medicine whose active substance is Lidocaine Hydrochloride injection. The official product information classifies it as a Class Ib antiarrhythmic agent, indicating its use for stabilizing heart rhythms.


Q: Is Xylocard used for pain relief like the local anesthetic forms of lidocaine?

A: No, the official regulatory indications for the intravenous (IV) form of Xylocard are restricted to the treatment of certain unstable heart rhythms known as ventricular arrhythmias. While the active ingredient lidocaine is also used as a local anesthetic for pain, the IV formulation is approved and regulated specifically for cardiac purposes.


Q: How quickly does Xylocard start working after it is administered?

A: The antiarrhythmic effect is described in official documents as having a rapid onset of action following an intravenous bolus. The stabilizing effect is noted in clinical data to often begin within about 1.5 minutes after administration, supporting its use in acute cardiac events.


Q: How long does the effect of Xylocard usually last?

A: The effect of a single intravenous bolus is generally short, typically described as lasting 10 to 20 minutes. A continuous intravenous infusion is typically initiated afterward, as part of the established protocol, to maintain stable drug levels.


Q: Is it normal to feel a metallic taste during or after Xylocard administration?

A: A metallic taste is described in medical literature as a known early symptom that may be associated with increasing drug levels in the bloodstream. Official documentation notes that if this occurs, it may be associated with rising drug levels that require continuous clinical assessment.


Q: Does Xylocard interact with alcohol?

A: Regulatory sources generally advise consulting a healthcare professional regarding all substances, including alcohol, during treatment with any medication that affects the heart or central nervous system. Specific interaction details with the IV formulation are typically managed within the professional healthcare setting.


Q: What are the known risks of using Xylocard during pregnancy?

A: Regulatory documents state that use of this drug during pregnancy is recommended only if clearly needed and the potential benefit is determined to outweigh the potential risk. The official product information indicates that local anesthetics may be able to rapidly cross the placenta.


Q: Is Xylocard present in breast milk, and what is the general guidance for nursing mothers?

A: Official information confirms that lidocaine is excreted into human milk in small amounts. Regulatory documents state that caution should be exercised when the medicine is administered to a nursing woman, and that individual professional judgment is required in this context.


Q: Is Xylocard safe to use in patients who have liver problems?

A: The official product information advises caution and requires that the dosage be reduced for patients with hepatic impairment (liver dysfunction). This is because Xylocard is metabolized in the liver, and dysfunction can slow clearance, potentially leading to drug accumulation and toxicity.


Q: Is Xylocard a medicine that can be kept at home for self-administration?

A: No, this medicine is for parenteral administration via the intravenous route and is explicitly restricted to use in healthcare settings. It requires immediate access to continuous ECG monitoring and resuscitative equipment, which is not available in a home setting.


Q: Are there any over-the-counter medicines or supplements that should not be taken with Xylocard?

A: Regulatory documents advise that healthcare providers must be informed of all medicines being taken—including prescription, over-the-counter drugs, herbal remedies, and supplements. This step supports the healthcare team in assessing the potential for any drug-drug interactions before the medicine is administered.


Q: Does Xylocard have any non-medicinal ingredients that can cause a reaction?

A: Yes, official labeling states that the medicine is contraindicated in patients who are hypersensitive (allergic) to the drug or to any ingredient in the formulation. Official product information notes that this restriction includes both the active substance and any non-medicinal components or preservatives in the preparation.


Q: Can Xylocard be used to treat atrial fibrillation or flutter?

A: The drug is primarily indicated for serious ventricular arrhythmias. Official documents caution that administration to patients with atrial fibrillation or flutter may potentially lead to an acceleration of the ventricular rate, which is considered a potentially serious adverse effect.


Q: Are there different concentrations or strengths of Xylocard injection?

A: Yes, Xylocard is available in different concentrations and strengths (such as 10 mg/mL or 20 mg/mL) depending on the specific use and the required dosing. The specific concentration must often be diluted by a healthcare professional prior to its use in a continuous infusion.


Q: Can Xylocard be used in patients who have a pacemaker?

A: The medicine is formally contraindicated in patients with severe degrees of heart block in the absence of a pacemaker. The official document does not extend the contraindication to patients who have a functioning pacemaker in place.


Q: How does Xylocard affect the central nervous system (CNS)?

A: The effects on the Central Nervous System (CNS) are generally described as dose-related. Early signs may include feeling light-headed, dizzy, drowsy, or experiencing tremor. At higher plasma concentrations, the risk of more serious effects, such as convulsions, increases, which is why close monitoring is required.


Q: Is Xylocard commonly associated with the side effect of ringing in the ears (tinnitus)?

A: Tinnitus (ringing in the ears) is officially listed in regulatory documents as an early central nervous system (CNS) manifestation. Official documents describe tinnitus as an early sign of central nervous system effects that is associated with higher plasma concentrations.


Q: Can Xylocard be used in infants or young children?

A: Official product monographs for Xylocard may state that the safety and effectiveness in pediatric patients have not been established for the antiarrhythmic indication. In such cases, regulatory documents often state that safety and effectiveness in pediatric patients have not been established due to lack of definitive data.


Q: What is methemoglobinemia, and is it a possible side effect of Xylocard?

A: Methemoglobinemia is a reported, rare, but serious adverse effect associated with certain local anesthetic agents, including lidocaine. This condition involves a change in the form of hemoglobin that may reduce the blood's capacity to carry oxygen.


Q: Does Xylocard require a prescription?

A: Yes, Xylocard (Lidocaine Hydrochloride Injection) is classified by regulatory agencies as a prescription-only medicine (Rx only). It must be administered and overseen by licensed healthcare professionals.

How should Xylocard be stored and disposed of?

How to Store and Dispose of Xylocard (Lidocaine HCl Injection)

The official storage and handling instructions for Xylocard are based on regulatory requirements to maintain product integrity and safety.

Storage Requirement Official Regulatory Statement
Temperature Store at Controlled Room Temperature, typically 20 C to 25 C (68 F to 77 F). Avoid excessive heat.
Handling Aseptic technique is required. Visually inspect the solution for particulate matter or discoloration before use; do not administer if compromised.
Single-Use Rule Single-dose vials and syringes (preservative-free) are for single use only. Any unused portion must be immediately discarded.
Disposal Used needles, syringes, and vials must be handled as medical waste. Disposal must follow facility and local regulatory requirements for sharps and pharmaceutical waste.

These instructions define the mandatory temperature controls, emphasize the single-use nature of the injection, and specify the required disposal as regulated medical waste.

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

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