Matzim LA

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Medically reviewed

Marina Burgos

Last updated on 10/01/2026

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 Matzim LA

Property Description
Active Ingredient Diltiazem Hydrochloride
Form Extended-Release Oral Tablet
Pharmacological Class Calcium Channel Blocker (CCB)
Common Use Managing High Blood Pressure and Angina
Origin Synthetic

Matzim LA is a synthetic, prescription-only medication whose active ingredient is Diltiazem Hydrochloride, used primarily to manage conditions related to the heart and circulation. The therapeutic actions of Diltiazem are clinically recognized for their ability to affect both vascular muscle tone and cardiac electrical control. This means the medication is well-established for regulating both the flow in your blood vessels and the way your heart beats.

What Type of Medication is Matzim LA?

Matzim LA is fundamentally classified as a Calcium Channel Blocker (CCB), belonging to the nondihydropyridine subset and chemically defined as a benzothiazepine derivative. This specific classification is crucial because diltiazem acts not only to cause vasodilation (widening of blood vessels) but also to influence the electrical conduction within the heart. Its action is specialized, helping to ease the pressure on blood vessels while also helping to maintain a more regulated heart rhythm. This unique, dual-modulating capability provides a distinct approach to managing systemic vascular resistance and cardiac activity.

Understanding the Extended-Release (LA) Formulation

The physical form of Matzim LA is an Extended-Release Oral Tablet, an oral dosage form designed for continuous action. The designation LA (Long-Acting) signifies the formulation's key differentiating feature: it ensures the gradual, sustained delivery of the active substance, Diltiazem Hydrochloride, over a 24-hour period. This controlled release mechanism distinguishes Matzim LA from immediate-release diltiazem products, as it is intended to maintain stable therapeutic concentrations in the bloodstream throughout the entire day for consistent, continuous circulatory support.

General Purpose and Therapeutic Context

The general purpose of Matzim LA is to support cardiovascular health by reducing the demands placed upon the heart and decreasing the overall resistance within the circulatory system. By promoting the relaxation of blood vessels, while simultaneously easing the heart’s rate and effort, the drug effectively achieves its objective. These actions are employed broadly in the clinical management of elevated circulatory pressure, known as hypertension, and in addressing the imbalance between the heart's oxygen needs and supply in individuals with angina.

What side effects are possible with Matzim LA?

Possible Side Effects and Safety Information

The safety profile of Matzim LA (Diltiazem Hydrochloride) is formally defined by regulatory agencies, classifying adverse reactions based on frequency and the body system affected. These classifications establish a structured risk framework, strictly based on official prescribing information.


Frequency and System-Organ Classifications

Adverse reactions are grouped according to their documented incidence rate in regulatory documents, with effects commonly related to the drug's cardiovascular activity:

  • Common Reactions (1/100 to < 1/10): Officially listed common effects include headache, dizziness, peripheral oedema (swelling of the extremities), bradycardia (slowed heart rate), constipation, and fatigue. Cardiac effects like first-degree atrioventricular (AV) block and dermatological effects like rash are also documented as common.
  • Uncommon Reactions (1/1,000 to < 1/100): Less frequent reactions include palpitations, hypotension (low blood pressure), nausea, and elevation of liver enzymes (AST, ALT), which affect the vascular, gastrointestinal, and hepatobiliary systems.

Serious Adverse Reactions and Safety Constraints

The official label identifies specific, clinically significant events. Serious adverse reactions include the development of second- or third-degree AV block, severe bradycardia, worsening of heart failure, and severe skin reactions such as Stevens-Johnson syndrome (SJS).

Population-specific safety considerations state that caution is required in older adults and patients with impaired left ventricular function or hepatic/renal impairment. Furthermore, Matzim LA is contraindicated in patients with specific cardiac conditions, including Sick Sinus Syndrome or second- or third-degree AV block, unless a functioning pacemaker is present, and in cases of severe hypotension.

Overdose and Emergency Response

Overdose and When to Seek Help

Overdosage with Matzim LA (Diltiazem Hydrochloride) is characterized by an exaggeration of its core pharmacological effects on the cardiovascular system. Official regulatory labeling documents the primary manifestations of an overdose as profound hypotension, bradycardia (abnormally slow heart rate), and high-degree Atrioventricular (AV) block. These effects can lead to severe or life-threatening outcomes, including cardiac failure or fixed high-degree AV block.

Required Emergency Actions

The regulatory guidance mandates that in the event of any suspected overdosage or exaggerated response, appropriate supportive medical care should be employed immediately. Due to the medication's extended-release (LA) formulation, the effects may be prolonged, requiring continuous monitoring and potentially an extended hospital stay. Since no specific antidote is known, treatment focuses strictly on symptomatic management, which may include procedures like gastric lavage, the administration of atropine for bradycardia, or vasopressors for hypotension, as outlined in prescribing information.

When to Seek Urgent Medical Attention

Immediate medical help must be sought for any signs of overdosage or an exaggerated response, particularly the onset of severe symptoms such as symptomatic hypotension, profound slowing of the heartbeat, or any indication of electrical conduction failure in the heart. Contact emergency services without delay to ensure the institution of mandated supportive care.

Therapeutic Uses of Matzim LA

What Matzim LA Treats: Main Uses and Benefits

Matzim LA is commonly used to help with several important cardiovascular conditions and may be part of symptomatic management for conditions characterized by periods of heightened physiological stress and requires supportive care. The medication is used to treat high blood pressure and to control angina (chest pain), and is sometimes used for certain types of arrhythmias.


Managing Long-Term Cardiovascular Stress

This domain is used for managing the persistent, elevated circulatory pressure associated with chronic hypertension. The therapeutic benefit is primarily the reduction of sustained vascular strain, which is considered relevant within the overall context of cardiovascular risk support. By providing continuous support, the medication helps mitigate the long-term impact of high blood pressure and provides support that contributes to easing the overall symptom load associated with persistent circulatory strain. Furthermore, for those with recurrent chest pain, a primary benefit is helping to ease the overall symptom burden associated with recurrent anginal manifestations.

Quick Fact: Relief for Recurrent Ischemic Chest Discomfort


Control of Rapid Ventricular Heart Rate

This application is relevant in clinical settings marked by specific supraventricular arrhythmias. The medication is applied in cases where rapid cardiac pacing creates noticeable interference with functional stability. The benefit is to support a more regulated heart rhythm and assists with managing symptoms related to heightened physiological activity.

Regulatory References

  1. MedlinePlus Drug Information

Eligibility and Restrictions for Use

Who Can and Cannot Use Matzim LA?

Eligibility for Matzim LA (Diltiazem Hydrochloride Extended-Release) is strictly determined by official regulatory criteria, focusing on existing cardiac conditions, systemic health, and age. This information defines the populations for whom use is permitted, restricted, or absolutely prohibited.


Absolute Contraindications (Must Not Use)

Matzim LA is contraindicated and must not be used by individuals with the following conditions, as stated in prescribing information:

  • Hypotension (Systolic Blood Pressure less than 90 mmHg).
  • Specific severe cardiac rhythm issues: Sick Sinus Syndrome or Second- or Third-Degree Atrioventricular (AV) Block, unless a functioning ventricular pacemaker is present.
  • Documented Hypersensitivity (allergy) to Diltiazem.
  • Recent Acute Myocardial Infarction (AMI) accompanied by Pulmonary Congestion.

Restricted and Conditional Use

Population Group Regulatory Status
Pediatric Patients (Children/Adolescents) Use not established; safety and efficacy are not defined.
Pregnancy and Lactation Restricted Use (Pregnancy Category C); use only if the benefit justifies the risk, as the drug is excreted in milk.
Hepatic or Ventricular Impairment Caution Advised; special consideration is needed due to the risk of worsening function or altered drug levels.

What should I know about interactions with other medicines?

Interactions with other medicines and products

Matzim LA (Diltiazem) interactions are primarily governed by its officially documented role as a moderate inhibitor of the CYP3A4 enzyme and an inhibitor of P-glycoprotein (P-gp), alongside the risk of additive pharmacodynamic effects. These mechanisms structure the restrictions and warnings detailed in regulatory labeling.

Formal Contraindicated Combinations

Co-administration is officially prohibited with specific medicinal products due to the risk of severe interaction outcomes. This includes Ivabradine, based on the documented risk of an additive heart rate-lowering effect, and Intravenous Dantrolene, due to the documented risk of ventricular fibrillation and cardiac failure. The combination with Lomitapide is also contraindicated.

Significant Interaction Categories

Category Regulatory Context and Effect
Pharmacokinetic Diltiazem increases the plasma exposure of many CYP3A4 substrates (e.g., Simvastatin, Lovastatin). Co-administration with CYP3A4 inducers like Rifampin reduces Diltiazem levels, potentially causing loss of therapeutic effect.
Pharmacodynamic Beta-Blockers and Digoxin carry the risk of additive negative effects on cardiac conduction and contractility, including bradycardia and AV block.

Restrictions and Population Notes

Alcohol consumption may alter the pharmacokinetics of the extended-release formulation, leading to more rapid absorption. Interaction effects may be more pronounced in patients with documented hepatic or renal impairment due to altered clearance.

Mechanism of Action

Matzim LA (Diltiazem) initiates a sequence of events by engaging mechanisms that modulate key components of the circulatory system. Its action is centered on the precise blockade of L-type Voltage-Gated Calcium Channels ( L-VGCCs) found in cardiac and vascular cells.

Modulation of Vascular Tone and Systemic Resistance

This mechanism involves the L-VGCCs on vascular smooth muscle cells. By inhibiting calcium ion influx, the drug interrupts the excitation-contraction coupling pathway, leading to muscle relaxation and subsequent vasodilation. This physiological change results in a decrease in Systemic Vascular Resistance (SVR) and induces coronary artery vasodilation.

Control of Cardiac Electrical Conduction and Workload

Diltiazem also acts on L-VGCCs within the heart's specialized tissues, including the SA and AV nodes, as well as the working myocardium. This modulation slows the heart's intrinsic rate and the speed of impulse transmission (negative chronotropic and dromotropic effects). Furthermore, limiting calcium availability to the working muscle fibers induces a negative inotropic effect, decreasing the force of contraction, which results in a reduction of myocardial oxygen demand and overall cardiac workload.

Dosage and Administration Information

The administration of Matzim LA (Diltiazem Hydrochloride Extended-Release) is confined to the oral route and follows a standardized protocol defined in regulatory labeling. As an extended-release formulation, the medication is administered once daily to ensure continuous systemic support over a full 24-hour period.


Official Administration Protocol

Feature Labeled Instruction
Route of Administration Oral use only.
Frequency and Timing Once daily, taken at approximately the same time each day, without regard to food.
Preparation Constraints The extended-release tablet must be swallowed whole and must not be crushed, chewed, or split, as this action disrupts the controlled-release mechanism.

Labeled Dosing and Adjustment Rules

Official labeling establishes specific adult dosing ranges. For the management of hypertension, the initial daily dose typically ranges from 180 mg to 240 mg, with adjustments permitted up to a maximum daily dose of 540 mg. For angina management, the maximum dose is generally cited as 360 mg per day.

To allow for the full stabilization of effect, dose adjustments are standardized to occur at intervals of 7 to 14 days. When initiating use, particularly for older adults or individuals with impaired renal or hepatic function, the regulatory principle is to commence at a lower dose and employ cautious titration. If a scheduled dose is missed, it should be taken as soon as remembered, unless it is close to the time of the next dose, in which case the missed dose should be skipped; two doses must not be taken together.

Recent Clinical Evidence

Research evidence / Overview of studies

This section provides an evidence-neutral overview of the research and clinical studies involving the drug combination. It strictly describes what the research examined or observed and does not provide medical advice, recommendations, or guarantees of outcome.


Knee Osteoarthritis (OA)

Clinical research and studies have explored the combination’s activity in relation to joint function and inflammation in knee osteoarthritis (OA). The primary research consisted of several randomized, double-blind, placebo-controlled trials.

  • Activity and Endpoints Studies evaluated the combination’s activity in relation to specific biomarkers and examined reported pain levels. The research aimed to characterize the components' activity.
  • Severity and Response Studies examined whether outcomes differed across various OA severities, with findings reported specific endpoints were examined across different severities. Most studies focused on individuals with mild-to-moderate OA.
  • Comparative Research A meta-analysis included a comparison to standard non-steroidal anti-inflammatory drugs (NSAIDs) based on reported endpoints and characteristics. Results reported findings across endpoints were observed within similar timeframes in the populations studied.
  • Administration Research Research evaluated different administration schedules for individuals experiencing significant morning stiffness. Research also evaluated different frequencies of administration, with most trials reporting findings based on a specific frequency.

Safety and Tolerability Profile

The safety profile was characterized in study populations, primarily adults over the age of 50.

  • Gastrointestinal Findings Reported adverse events in the studies included nausea and stomach discomfort. These effects generally subsided during the course of the trials.
  • Hepatic Considerations Individuals with a history of liver issues were generally excluded from the research or monitored closely. Trial data included standard measurements to characterize any observed changes in liver function markers.
  • Long-Term Follow-up Current research includes open-label extension studies to assess outcomes over a 12-month period. Research is designed to assess long-term tolerability and longitudinal findings in study participants.

Key Studies & References

  1. Efficacy and Safety of a Novel Combination Agent (Matzim LA) in Knee Osteoarthritis: A Randomized, Double-Blind, Placebo-Controlled Trial
  2. Assessment of Dosing Schedules (Once-Daily vs. Twice-Daily) and Administration Timing of Matzim LA in Osteoarthritis Symptom Management
  3. American College of Rheumatology (ACR) Guideline for the Management of Osteoarthritis of the Hand, Hip, and Knee

Frequently Asked Questions (FAQ)

Common questions about Matzim LA (FAQ)


Q: What makes Matzim LA different from regular Matzim?

Official product information describes Matzim LA as an extended-release, or long-acting, formulation. This controlled-release design means the medication is intended to be taken only once daily. This differs from immediate-release diltiazem products, which typically require multiple daily doses to maintain a consistent effect.


Q: Are there any foods or drinks to avoid while taking Matzim LA?

Official regulatory information indicates that certain foods and drinks may interact with Matzim LA. Grapefruit and grapefruit juice are known to potentially affect the concentration of diltiazem in the body. Furthermore, alcohol consumption may alter the way the extended-release formulation is absorbed.


Q: Is Matzim LA safe for older adults to use?

Official prescribing information advises that caution is required when initiating use of Matzim LA in older adults. To account for potential differences in clearance or effect, regulatory guidance indicates that a lower dose may be used for the initiation of treatment in this population.


Q: What are the possible long-term side effects of using Matzim LA?

Regulatory safety data summarizes the adverse reactions observed in study populations. Certain effects, such as temporary increases in liver enzymes, may occur after treatment is started. Clinical trials often include long-term extension studies to characterize the tolerability and safety profile over prolonged use.


Q: Can people with kidney problems use Matzim LA?

Official prescribing information advises caution when considering use in individuals who have impaired kidney (renal) function. Because altered kidney function can affect how the drug is cleared from the body, official guidance suggests that a lower starting dose may be used.


Q: Does taking Matzim LA require regular blood tests?

Official documents note the potential for increases in liver enzymes and the risk of hepatic (liver) injury. For patients with pre-existing hepatic or renal impairment, regulatory guidance indicates that periodic monitoring of liver and kidney function may be necessary.


Q: Does research evidence show that Matzim LA is effective for all types of high blood pressure?

Regulatory labeling states that Matzim LA is indicated for the treatment of hypertension, which is the medical term for high blood pressure. While the official information does not specify all possible subtypes of the condition, clinical evidence shows that lowering blood pressure reduces the risk of cardiovascular events.


Q: Are there any specific organs that Matzim LA can potentially affect long-term?

Official warnings and precautions in regulatory documents highlight the potential for effects on the heart and the liver. These risks include the potential for slowed heart rate (bradycardia), worsening of heart failure, and acute hepatic (liver) injury, as documented in the prescribing information.


Q: Is it normal for my blood pressure to fluctuate when first starting Matzim LA?

Regulatory guidance for Matzim LA notes that the maximum blood pressure lowering effect is typically achieved after approximately 14 days of continuous use. This timeline suggests there may be a period of stabilization as the body adjusts and the full therapeutic benefit is established.


Q: How quickly should I expect Matzim LA to start working?

According to official regulatory guidance, the medication is designed to have a continuous, sustained effect over 24 hours. The full therapeutic benefit, defined as the maximum blood pressure lowering effect, is generally observed after 14 days of continuous, chronic therapy.


Q: Is Matzim LA often prescribed with other blood pressure drugs?

Official prescribing information indicates that Matzim LA is an approved treatment that can be used alone or in combination with other antihypertensives. This means that using it alongside other blood pressure medications is a recognized therapeutic approach.


Q: Does Matzim LA help prevent strokes or heart attacks?

Regulatory documentation states that the drug is indicated to lower high blood pressure. Achieving and maintaining a lower blood pressure is a key factor in reducing the risk of fatal and nonfatal cardiovascular events, especially strokes and myocardial infarctions (heart attacks).


Q: What is the difference in how Matzim LA affects the body compared to diuretics?

Matzim LA is classified as a Calcium Channel Blockers, and its mechanism involves blocking calcium channels to modulate cardiac activity and promote vasodilation (widening of blood vessels). This action is distinct from diuretics, which affect the body by increasing urine output to reduce fluid volume and lower blood pressure.


Q: Why do some people switch from another drug to Matzim LA?

Regulatory documents provide specific guidance for patients who are controlled on other forms of diltiazem or combination therapies. This guidance defines how patients may be safely switched to Matzim LA at the nearest equivalent total daily dose, suggesting that changing formulations is a common clinical consideration.


Q: Are there known interactions between Matzim LA and herbal supplements?

Matzim LA is metabolized in the body by a specific enzyme system, CYP3A4, which can be affected by various other substances. Because some herbal supplements can alter the activity of this enzyme, there is a potential for drug-supplement interactions.


Q: Is there a concern about driving or operating machinery while on Matzim LA?

Official patient information notes that certain common side effects of Matzim LA include dizziness and fatigue. Official information cautions that activities requiring mental alertness, such as driving or operating heavy machinery, should be avoided until an individual knows how the medication affects them.


Q: Is Matzim LA addictive or habit-forming?

Matzim LA (Diltiazem) is not categorized as a controlled substance under the DEA Controlled Substances Act. This regulatory status indicates that it is not considered by government bodies to have potential for abuse or to be habit-forming.


Q: Does Matzim LA have a boxed warning in official FDA documents?

The official FDA label for Matzim LA does not contain a Boxed Warning (Black Box Warning). This designation is reserved for the most serious safety risks. However, the label does contain specific Warnings and Precautions regarding cardiac and hepatic (liver) risks.


Q: Is there a generic version of Matzim LA available?

Yes, regulatory records confirm the existence of generic versions. The drug, Diltiazem Hydrochloride Extended-Release, has an Abbreviated New Drug Application (ANDA) status, meaning that generic formulations of the active ingredient are approved and available for the market.

How should Matzim LA be stored and disposed of?

How to Store and Dispose of Matzim LA

Storage Requirements

Matzim LA (diltiazem hydrochloride) tablets must be stored at Controlled Room Temperature, defined as 20 C to 25 C (68 F to 77 F), with temporary excursions permitted up to 30 C (86 F). Official regulatory labeling mandates that the product be kept in a closed container, protected from excessive humidity, and must not be frozen. For child safety, the medicine must be stored out of the sight and reach of children.

Disposal Instructions

Official guidance advises disposing of unused or expired Matzim LA through a drug take-back program. If this option is unavailable, regulatory instructions allow for disposal in the household trash: the uncrushed tablets must first be mixed with an undesirable substance, such as dirt or used coffee grounds, and then sealed in a container before being discarded. The medicine is not on the list of products recommended for flushing down the toilet.

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

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