Dilzem-CD

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Dilzem-CD

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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 Dilzem-CD

What is Dilzem-CD? Composition and Classification

Property Description
Active ingredient Diltiazem Hydrochloride
Form Extended-release capsule (sustained-release)
Pharmacological class Non-dihydropyridine Calcium Channel Blocker (CCB)
General purpose Management of conditions related to blood pressure and cardiac workload
Origin Synthetic chemical entity (Benzothiazepine derivative)

Dilzem-CD is a prescription-only medicine and a single-entity product whose active ingredient is Diltiazem Hydrochloride. This substance is a synthetic chemical entity, formally classified as a Benzothiazepine derivative. The core classification of the active compound, Diltiazem, places it within the high-level pharmacological class known as Calcium Channel Blockers (CCBs), also recognized as a Class IV antiarrhythmic agent. The defined composition of this medication is clinically recognized for providing a targeted therapeutic effect on the cardiovascular system.

The Role of Diltiazem as a Non-dihydropyridine CCB

Diltiazem is specifically designated as a Non-dihydropyridine type of Calcium Channel Blocker, a subcategory whose mechanism impacts both the vascular smooth muscle and the heart's electrical conduction system. This characteristic allows Diltiazem to influence cardiac rhythm directly, a differentiating feature from other CCBs. This means the medicine helps achieve rhythm control and lowers resistance to blood flow simultaneously. The pharmaceutical form of this medication is an Extended-release capsule, an oral dosage form where the "CD" denotes a sustained-release preparation designed for once-daily administration. This specialized formulation is recognized to ensure the Diltiazem ingredient is delivered slowly and consistently for continuous action across a 24-hour period.

General Purpose and Cardiovascular Benefit

The general therapeutic purpose of this medication is to reduce overall strain and workload on the heart and circulatory system. This is achieved through its core actions: promoting vasodilation (relaxing blood vessels), which decreases peripheral vascular resistance, and inducing a negative chronotropic effect (slowing the heart rate) alongside a negative inotropic effect (decreasing the force of heart contraction). Diltiazem is effective in lowering elevated blood pressure and decreasing the amount of oxygen the heart requires to pump blood. This mechanism is routinely utilized in patient management to stabilize high blood pressure or to relieve chest discomfort associated with increased cardiac oxygen demand.

Regulatory References

  1. Diltiazem - StatPearls - NCBI Bookshelf

What side effects are possible with Dilzem-CD?

Possible Side Effects and Safety Information

This information is based on the official safety documentation and regulatory findings for extended-release diltiazem formulations (such as Dilzem-CD).


Common and Expected Adverse Reactions

Adverse reactions reported in clinical trials at a frequency of 1% or more include:

  • Cardiovascular: Edema (swelling, particularly in the lower limbs), Bradycardia (slow heart rate), First-degree Atrioventricular (AV) block.
  • Nervous System: Headache, Dizziness.
  • Gastrointestinal: Constipation.
  • Other: Fatigue, Rash.

Serious Adverse Reactions

Official regulatory documents identify several serious adverse reactions, which require immediate medical attention. These include:

  • Severe Cardiac Effects: Development of second- or third-degree AV block (without a functioning pacemaker), symptomatic hypotension (severe low blood pressure), and worsening of congestive heart failure.
  • Systemic Risks: Rare instances of acute hepatic injury (liver damage, often reversible upon discontinuation), and severe, potentially life-threatening skin reactions such as Stevens-Johnson syndrome (SJS) and Toxic Epidermal Necrolysis (TEN).

Safety Restrictions and Contraindications

Dilzem-CD is contraindicated (must not be used) in patients with severe cardiac conditions including:

  • Sick Sinus Syndrome or Second-/Third-Degree AV Block (unless a functioning pacemaker is present).
  • Severe Hypotension (Systolic Blood Pressure below 90 mmHg).
  • Known hypersensitivity to the drug.

Special Safety Notes

  • Alcohol Interaction: Regulatory warnings state that alcohol increases the rate of drug release and systemic exposure, which increases the risk of adverse reactions. Alcohol consumption must be avoided while taking this medication.
  • Drug Interactions: The drug can affect the metabolism of other medicines (e.g., certain statins or immunosuppressants) by inhibiting the CYP3A4 enzyme, requiring monitoring and potential dose adjustments of the co-administered drug.

Overdose and Emergency Response

Overdose and When to Seek Help: Official Regulatory Information

This section outlines the officially documented overdose manifestations and mandated actions for Dilzem-CD (Diltiazem Hydrochloride), based strictly on government regulatory documents.

Documented Overdose Manifestations

An overdose with this medication primarily presents as a severe exaggeration of its effects on the cardiovascular system. According to regulatory labeling, documented clinical signs may include Profound Hypotension (severe low blood pressure), significant Bradycardia (abnormally slow heart rate), and various degrees of Atrioventricular (AV) Block.

Severe outcomes documented in official sources include Cardiac Failure, Sinus Arrest, and Fixed High-Degree AV Block.

Required Emergency Actions

Immediate medical attention is required for any suspected overdose. Official regulatory instructions explicitly state that appropriate supportive medical care must be employed immediately.

  • Mandatory Action: Immediately call emergency services or contact a Poison Control Center.
  • Monitoring Note: Due to the extended-release nature of Dilzem-CD, the effects can be prolonged, necessitating an overnight hospital stay for continuous monitoring, even if initial symptoms appear less severe.

Supportive Management

Treatment is supportive, as no specific antidote is officially documented in primary regulatory labeling. Officially described management procedures include initial measures like Gastric Lavage and the use of pharmacological agents to manage symptoms:

  • For Bradycardia: Administration of Atropine.
  • For Hypotension: Administration of Vasopressors (e.g., Dopamine).
  • For Severe Heart Block: Use of Cardiac Pacing.

Therapeutic Uses of Dilzem-CD

The primary role of Dilzem-CD is to provide support for symptomatic relief across specific chronic cardiovascular conditions. This extended-release formulation is commonly used for managing conditions that involve high pressure, preventing chest pain, and assisting with heart rate control.

This medication is relevant for the long-term management of Systemic Hypertension and the treatment of Angina Pectoris, including both chronic stable angina and angina due to coronary artery spasm, as well as for ventricular rate control in certain supraventricular tachyarrhythmias.

Management of Sustained High Arterial Blood Pressure

Dilzem-CD is relevant for the long-term management of Systemic Hypertension, a condition characterized by sustained, elevated arterial pressure. Its therapeutic benefit includes the sustained management of elevated arterial pressure, an established approach in treatment that supports the overall well-being of the cardiovascular system during periods of sustained pressure.

“This medication is frequently used in clinical settings where long-term symptomatic support for cardiovascular stability is needed.”

Prevention and Control of Angina Chest Pain

This medication is applicable for the treatment and prophylaxis of Angina Pectoris. In the context of angina, it supports relief from discomfort and contributes to easing the overall symptom load by addressing the frequency and intensity of chest discomfort episodes. This assists with maintaining functional stability and allows patients to experience greater tolerance for routine activity.

Quick Fact: Relief for Episodic Chest Discomfort The medicine is commonly used to address the recurrent nature of chest pain that interferes with daily functioning.

Rate Control for Abnormally Fast Heart Rhythms

Dilzem-CD is commonly used in clinical settings involving certain supraventricular tachyarrhythmias, such as Atrial Fibrillation or Atrial Flutter, where the heart is beating abnormally fast. Its practical benefit is relevant for ventricular rate control, which helps stabilize the rapid heart rhythm and supports the patient during difficult symptomatic episodes by easing distress.

Regulatory References

  1. NIH MedlinePlus overview of Diltiazem

Eligibility and Restrictions for Use

Official Eligibility Map: Who Can and Cannot Use Dilzem-CD

This section outlines the officially documented eligibility and non-eligibility rules for Diltiazem Hydrochloride Extended-Release (Dilzem-CD), based strictly on government regulatory labeling.


Contraindicated Populations (Must Not Use)

Condition
Sick Sinus Syndrome or Second- or Third-Degree AV Block (unless a functioning pacemaker is present)
Severe Hypotension or Cardiogenic Shock
Acute Myocardial Infarction complicated by Pulmonary Congestion
Left Ventricular Failure with pulmonary congestion
Atrial Fibrillation/Flutter with an Accessory Bypass Tract (e.g., Wolff-Parkinson-White Syndrome)
Known Hypersensitivity to diltiazem hydrochloride or any component

Population Restrictions and Conditional Use

Population/Condition Regulatory Stance
Pediatric Population (Children/Adolescents) Safety and efficacy have not been established; not recommended.
Pregnancy and Lactation (Breastfeeding) Contraindicated (prohibited)
Impaired Hepatic Function Use with caution; close monitoring required.
Impaired Renal Function Use with caution; monitoring advised.
Older Adults (Geriatric) Use is permitted, but caution is required due to potential age-related organ impairment.

Eligibility for use is strictly defined by these regulatory classifications and must be determined by a healthcare provider.

What should I know about interactions with other medicines?

Interactions with other medicines and products

Dilzem-CD (Diltiazem) can significantly interact with many other medicines due to two primary mechanisms: its effects on the heart's electrical system and its role as a metabolic enzyme inhibitor. Concomitant use with ivabradine or lomitapide is contraindicated (not permitted) due to the high risk of serious adverse effects.

Diltiazem is a moderate inhibitor of the CYP3A4 enzyme and a P-glycoprotein (P-gp) transporter inhibitor. This means it can raise the blood levels of numerous other drugs metabolized by these systems, potentially leading to increased effects or toxicity. Medicines affected include certain statins (e.g., simvastatin, requiring a dose limit of 20 mg/day), immunosuppressants (e.g., cyclosporine, tacrolimus), and some oral anticoagulants. Dosage adjustments for the interacting drug or close monitoring may be necessary.

Co-administration with agents that affect cardiac function, such as beta-blockers (e.g., propranolol) or digitalis/digoxin, can produce additive effects on the heart's conduction. This combined pharmacodynamic effect increases the risk of slow heart rate or atrioventricular (AV) block, requiring careful clinical supervision. Additionally, simultaneous consumption of alcohol with the CD formulation is not advised, as it can alter the drug's absorption and increase systemic exposure.

Mechanism of Action

Diltiazem, the active component of Dilzem-CD, is classified as a non-dihydropyridine calcium channel blocker. Its mechanism involves selectively targeting and inhibiting the L-type voltage-gated calcium channels in the cardiovascular system.


Blocking Calcium Channels in Cardiac Electrical Systems

The drug acts on these channels within the heart's sinoatrial (SA) and atrioventricular (AV) nodes. By inhibiting the influx of calcium ions ( Ca^2+) necessary for the slow inward current, the mechanism results in a negative chronotropic effect (slowing the heart rate) and a negative dromotropic effect (slowing electrical conduction velocity through the AV node).


Reducing Myocardial Contraction and Workload

Diltiazem also targets the L-type Ca^2+ channels in myocardial muscle cells. Restricting calcium entry limits the cellular process required for contraction, leading to a negative inotropic effect (decreased force of heart contraction). This action decreases the heart muscle's workload and its oxygen consumption ( MVO2).


Inducing Systemic and Coronary Vasodilation

Simultaneously, the same channel-blocking mechanism occurs in vascular smooth muscle cells lining the arteries. Inhibiting Ca^2+ influx prevents the muscle from contracting, causing the vessels to relax and widen (vasodilation). This relaxation reduces the Systemic Vascular Resistance (SVR), which represents the impedance to blood flow.

Dosage and Administration Information

Official Administration Guidelines for Dilzem-CD

Dilzem-CD is an oral, extended-release capsule formulation of diltiazem hydrochloride, and its use is governed by standard administration protocols. The purpose of the extended-release design is to ensure a gradual and consistent delivery of the medication over 24 hours.

Route and Dosing Frequency

Administration Detail Official Instruction
Route of Administration Oral.
Dosing Frequency Once daily (q.d.), taken at approximately the same time each day.
Standard Adult Dose (Starting) Typically ranges from 180 mg to 240 mg once daily, depending on the indication.
Maximum Recommended Dose Generally up to 540 mg once daily.

Proper Handling and Titration

Crucial instructions are provided to maintain the integrity of the controlled-release mechanism:

  • Do Not Alter Capsule: The capsule must be swallowed whole. It is explicitly stated that the capsule must not be crushed, chewed, or divided to prevent the immediate release of the entire dose.
  • Timing: The medication can generally be taken with or without food, although taking it consistently is recommended for chronic therapy.
  • Dose Adjustment: Dosage adjustments should not be made daily. Instead, the dose should be gradually increased, if necessary, based on patient response after a sustained period of chronic therapy, typically in intervals of 7 to 14 days.

Specific Population Rules

For certain patient groups, a cautious approach is specified. Older adults, for instance, may respond to a lower initial starting dose (e.g., 120 mg once daily). Caution is advised in patients with impaired liver or kidney function, although specific dose adjustment values are often not provided in standard prescribing guidelines.

Recent Clinical Evidence

Recent Clinical Evidence for Dilzem-CD (Diltiazem Extended-Release)

The extended-release formulation of diltiazem, commonly available as Dilzem-CD, has been the subject of multiple clinical trials primarily focused on its labeled uses: the management of hypertension (high blood pressure) and chronic stable angina (chest pain).


Findings in Hypertension

Research indicates that extended-release diltiazem may contribute to blood pressure reduction over a 24-hour period, making it suitable for once-daily dosing. In studies involving patients with essential hypertension, different doses of extended-release diltiazem have been associated with a dose-dependent reduction in diastolic blood pressure compared to placebo. A consistent reduction in blood pressure is an important factor in lowering the overall risk of associated cardiovascular events, such as stroke and myocardial infarction (heart attack).

Findings in Chronic Stable Angina

In patients with chronic stable angina, clinical evidence suggests that diltiazem may increase exercise tolerance. This observed improvement is thought to be related to the drug's effect on heart rate and blood pressure during exercise, which subsequently reduces the heart's oxygen demand. Comparative trials have indicated that diltiazem may contribute to an increase in the time until the onset of chest pain or signs of ischemia during exercise testing. A notable finding from some studies suggests that dosing the extended-release formulation in the evening may be associated with a greater improvement in exercise tolerance during the morning hours, a time often considered a high cardiovascular risk period.

Additional Observational Data

Beyond the main indications, diltiazem's property of slowing the conduction in the atrioventricular (AV) node has also been leveraged in trials for the rate control of certain atrial arrhythmias, such as atrial fibrillation. Studies have consistently noted that the drug's extended-release delivery system is designed to provide sustained plasma concentrations, which is essential for maintaining effects throughout the day and night.

Frequently Asked Questions (FAQ)

Common questions about Dilzem-CD (FAQ)


Q: What happens if I accidentally take two doses of Dilzem-CD at once?

Taking more than the prescribed amount of Dilzem-CD may lead to an overdose. According to official regulatory documents, known pharmacological effects of diltiazem may include severely low blood pressure or serious cardiac rhythm disturbances, such as an abnormally slow heart rate (bradycardia) or a high-degree heart block. Because an overdose requires specialized clinical management, individuals should seek immediate medical assistance.


Q: How long does it take for Dilzem-CD to start working?

Dilzem-CD is an extended-release medicine, meaning it is formulated to deliver the drug consistently over a 24-hour period. Studies indicate that the concentration of the drug in the blood typically peaks about 10 to 14 hours after a dose. However, the full effect on blood pressure control is usually gradual. Official information indicates that stable concentrations, associated with a therapeutic response, are generally achieved after about two weeks of therapy.


Q: What should I do if I forget to take my Dilzem-CD dose?

Official patient information advises that for a missed dose, the recommended instruction is to take it as soon as it is remembered. If it is already close to the time for the next scheduled dose, the instruction is to skip the one that was missed and return to the regular dosing schedule. It is typically advised that a double dose should not be taken to compensate for a missed dose.

How should Dilzem-CD be stored and disposed of?

How to Store and Dispose of Dilzem-CD?

Dilzem-CD (diltiazem hydrochloride extended-release capsules) must be stored at Controlled Room Temperature, specifically at 25 C (77 F), with permitted fluctuations between 15 C to 30 C (59 F to 86 F).

Required Protection and Packaging

The capsules must be protected from excessive humidity and must be kept in a tightly closed, light-resistant container. The official labeling mandates that the product be stored out of reach of children and kept in packaging with a child-resistant closure.

Official Disposal

To dispose of expired or unused Dilzem-CD, individuals should consult a healthcare professional or pharmacist for guidance. Disposal must always be performed safely and in accordance with local regulations for pharmaceutical waste.

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

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