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Нитролонг

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Нитролонг

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 Нитролонг

What is Нитролонг (Nitrolong)?

Property Description
Active Ingredient Nitroglycerin (Glyceryl Trinitrate)
Pharmacological Class Organic Nitrate / Antianginal Agent
Common Use Prevention and relief of chest pain (angina pectoris)
Origin Synthetic Compound
Primary Action Vasodilation (widening of blood vessels)

Classification and Purpose

Нитролонг is a recognized brand name for a medication whose active component is nitroglycerin, chemically known as glyceryl trinitrate. This drug belongs to the class of organic nitrates, which are classified as potent vasodilators.

Nitroglycerin acts by stimulating the production of nitric oxide, an agent that causes the relaxation of smooth muscles within blood vessel walls. This action reduces the workload on the heart, making it an essential antianginal agent used to prevent and manage chest pain (angina pectoris) caused by coronary artery disease.

Form and Availability

Unlike fast-acting, immediate-release forms of nitroglycerin, Нитролонг is often supplied as a controlled-release tablet or capsule. This pharmaceutical distinction means the active ingredient is released slowly into the body over several hours. This design is intended for patients with stable angina to provide sustained prophylactic protection against recurring chest pain throughout the day. Various formulations of nitroglycerin are utilized for the treatment and prophylaxis of angina, supporting its established role in long-term cardiac management.

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What side effects are possible with Нитролонг?

Possible Side Effects and Safety Information

The safety profile of Нитролонг, which contains the active ingredient nitroglycerin, is primarily characterized by effects related to its potent vasodilatory action, as documented in official regulatory labeling.


Official Adverse Reaction Frequencies

Adverse reactions are classified based on frequency in regulatory documents. The most commonly reported effects reflect the drug's impact on the cardiovascular and nervous systems:

  • Very Common (Affects 1 in 10 people or more): The most frequently documented reaction is Headache.
  • Common (Affects 1 to 10 in 100 people): Hypotension (low blood pressure), Dizziness, Orthostatic Hypotension (dizziness upon standing), Tachycardia (increased heart rate), Nausea, and Vomiting.

Uncommon reactions may include allergic skin reactions and, in some cases, enhanced symptoms of angina (paradoxical angina).


Safety Constraints and Serious Reactions

Official labels detail serious adverse reactions and conditions where use is restricted. Circulatory collapse, sometimes accompanied by syncope (fainting), is documented as an uncommon but serious adverse reaction. Methemoglobinemia is a rare, but clinically important, reaction listed.

Administration is absolutely contraindicated with certain medications, including PDE-5 inhibitors (like sildenafil) and soluble guanylate cyclase stimulators, due to the significant risk of severe, life-threatening hypotension. The drug is also contraindicated in patients with conditions involving increased intracranial pressure (e.g., head trauma) or severe anemia.

Time- and Exposure-Related Notes: Regulatory information notes that the development of pharmacological tolerance (diminished effect) may occur with prolonged, continuous exposure. The safety and effectiveness of the medication have not been established for pediatric use.

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Overdose and Emergency Response

Overdose Scope

Documented Overdose Presentations: Overdose symptoms primarily relate to severe vasodilation. Manifestations documented in regulatory sources include profound severe hypotension, a persistent throbbing headache, vertigo, palpitations, confusion, and dizziness. Severe toxicity can cause the skin to become initially flushed and perspiring, later turning cold and cyanotic (bluish discoloration of lips, fingers, or toes) due to methemoglobinemia, a condition particularly noted after massive doses.

Critical Outcomes and Emergency Action: Life-threatening outcomes include syncope (fainting), circulatory failure, shock, seizures, and coma. Immediate medical help is required if the person has collapsed, is having trouble breathing, or cannot be awakened. Regulatory documents advise calling emergency services or a poison control center immediately upon suspected overdose.

Overdose Management: Management is focused on supportive care to reverse the effects of severe hypotension and restore adequate tissue perfusion. Treatment may involve elevation of the extremities and central volume expansion with intravenous fluids. Vital signs, including blood pressure, pulse, and respiratory rate, are continuously monitored, and symptoms are treated specifically.

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Therapeutic Uses of Нитролонг

What Нитролонг Treats: Main Uses and Benefits

Нитролонг, which contains the active ingredient glyceryl trinitrate, is commonly used across conditions presenting with acute episodes. The medication is applied in addressing symptoms associated with acute or episodic changes and is particularly relevant in contexts involving heightened systemic burden. Its core therapeutic domain is to provide supportive relief when symptoms interfere with routine activities, specifically those symptoms related to physical discomfort in the chest.

Main applications for this medication are in the management of episodes of angina (chest pain) and its prevention. The patient benefit is that it helps maintain a sense of stability when symptoms are more noticeable, providing support that helps ease the overall symptom burden.

The medication may be part of symptomatic management applied when appropriate prior to activity that may intensify symptoms temporarily. It assists with maintaining functional stability during symptomatic periods. This approach is commonly used when short-term symptomatic assistance is needed for conditions involving episodic or fluctuating manifestations.


Quick Fact: Relief for Physical Discomfort


Regulatory References

  1. NIH MedlinePlus Drug Information
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Eligibility and Restrictions for Use

Who Can and Cannot Use Нитролонг?

The eligibility for using Nitrolong (nitroglycerin) is defined by regulatory bodies through specific contraindications and population restrictions. The medicine is primarily approved for the adult population.

Use is absolutely prohibited for patients who are concurrently taking certain medications, including Phosphodiesterase-5 (PDE-5) Inhibitors (e.g., sildenafil) or Soluble Guanylate Cyclase (sGC) Stimulators (e.g., riociguat).

Furthermore, the medicine is contraindicated in populations with specific physiological states, such as Severe Anemia, Increased Intracranial Pressure, Acute Circulatory Failure or Shock, or known Hypersensitivity to nitrates. Patients with certain cardiac conditions, including Constrictive Pericarditis or Pericardial Tamponade, must not use this medicine.

For certain populations, use is conditional or requires caution. Use is not recommended in pediatric patients because safety and effectiveness have not been established. In geriatric patients, careful dose selection is necessary. Use during pregnancy is restricted to situations where the benefit clearly outweighs potential fetal risk, and use during lactation is cautioned due to unknown excretion status. Conditional use is also specified for patients who are already hypotensive or volume-depleted.

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What should I know about interactions with other medicines?

Interactions with other medicines and products

Нитролонг (Nitroglycerin) has documented interaction patterns that are defined by formal regulatory constraints. The most critical constraint is the Absolute Contraindication with Phosphodiesterase Type 5 (PDE-5) Inhibitors (e.g., Sildenafil, Tadalafil) and Soluble Guanylate Cyclase (sGC) Stimulators (e.g., Riociguat). Co-administration with these agents is formally prohibited due to the risk of severe, life-threatening hypotension resulting from an extreme potentiation of the vasodilatory effect.

The official profile details several pharmacokinetic and pharmacodynamic interactions. Concomitant use with Aspirin may decrease the clearance of nitroglycerin, which is documented to enhance its effects. Conversely, intravenous nitroglycerin may reduce the anticoagulant effect of Heparin and decrease the thrombolytic effect of Alteplase.

Pharmacodynamic cautions include documented additive hypotensive effects when combined with alcohol, other antihypertensive drugs, and Phenothiazines. Furthermore, regulatory labeling imposes a strict timing-based separation rule for nitroglycerin following the use of certain PDE-5 Inhibitors, specifying a prohibited use window of 24 to 48 hours depending on the specific inhibitor. These official classifications define the necessary restrictions on co-administration.

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Mechanism of Action

How Нитролонг Works: Mechanism of Action


The molecule requires bioactivation within vascular smooth muscle cells, where it is converted into its active mediator, Nitric Oxide (NO). This conversion step is catalyzed by the mitochondrial enzyme Aldehyde Dehydrogenase 2 (mALDH2). The resulting NO molecule directly activates the enzyme soluble Guanylate Cyclase (sGC), which synthesizes the second messenger, cyclic Guanosine Monophosphate (cGMP).

Elevated cGMP levels initiate a cascade that leads to the dephosphorylation of myosin light chains, resulting in the relaxation of the blood vessel walls. This action modulates vascular tone, causing widespread vasodilation with a notable preference for systemic veins over arteries (venodilation).

This extensive venodilation increases the capacity of the venous system, which reduces the volume of blood returning to the heart (preload). By decreasing this filling pressure, the molecule lowers the heart's overall workload and oxygen demand, while also facilitating the dilation of the coronary arteries.

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Dosage and Administration Information

The administration of Нитролонг, which contains glyceryl trinitrate, is governed by established protocols designed for its role as a sustained-release prophylactic medication. These parameters focus on high-level dosing rules and handling requirements.

Category Standard Administration Protocol
Route of Administration The designated route is oral administration via an extended-release capsule or modified-release tablet.
Dosing Schedule Dosing is individualized, typically initiated at the lower available strengths (e.g., 2.6 mg or 6.5 mg). The usual regimen involves administration two or three times daily.
Preparation Requirements The modified-release unit must be swallowed whole and must not be chewed or crushed to maintain the integrity of its controlled-release mechanism.
Age-Group Rules Geriatric Patients: Dosing requires caution and should be tailored to individual needs. Pediatric Patients: Use is not established as safety and efficacy have not been demonstrated.
Special Procedural Conditions Treatment requires a 10 to 12 hour nitrate-free interval daily, achieved through non-uniform dosing, to prevent the development of pharmacological tolerance. This form is not indicated for aborting acute episodes.

Resulting Procedural Structure

The administration protocol specifies the use of this medicine as a prophylactic agent with strict, time-dependent constraints. This structure requires oral delivery and adherence to a non-uniform dosing schedule to secure the daily nitrate-free interval, which is a core principle for long-term functional use. When long-term treatment is concluded, the instructions require the dosage to be reduced gradually over several days to avoid a potential exacerbation of symptoms.

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Recent Clinical Evidence

Research Evidence / Overview of Studies for Нитролонг

Evidence for Use in Stable Angina Pectoris

The research base for long-acting nitroglycerin formulations, such as Нитролонг, includes Randomized Controlled Trials (RCTs). These studies were designed to compare the controlled-release formula against placebo in studies involving adults with stable angina pectoris. The trials were often conducted over short, defined time intervals, and researchers used them to explore outcomes in conditions characterized by fluctuating or episodic manifestations of pain.

The findings from these controlled trials and resulting meta-analyses describe patterns of change measured during the study period between the active medicine and the comparator. Research has explored outcomes related to physical discomfort and functional imbalance that were monitored in the studies. Specifically, studies report the differences in weekly frequency of angina episodes measured between the active medicine and the control groups.


Outcomes Measured in Clinical Trials

Studies focusing on this medicine also evaluated objective measures of physical capability in relation to the medicine. Research examined the use of specialized functional testing, such as exercise on a treadmill. The primary outcomes studied in these tests involved monitoring physiological strain, specifically recording the total duration of exercise performed before symptoms appeared or before certain physiological changes were detected. Furthermore, studies monitored the consumption of short-acting rescue nitroglycerin, an outcome that helps contextualize how patients reported their need for symptomatic assistance during episodes of heightened symptom activity.


Uncertainties and Limitations in the Research Base

Evidence highlights what is known—and what is still uncertain. A significant limitation consistently observed in the research is the problem of tolerance development. Data show patterns suggesting tolerance development when the medicine is taken continuously without a break. This finding is relevant to studies exploring durability of response. Furthermore, studies exploring the long-term impact of this class of medicine on serious outcomes, such as all-cause mortality or myocardial infarction, do not describe patterns related to a reduced risk on these specific measures.

Key Studies & References

  1. NITROGLYCERIN EXTENDED-RELEASE CAPSULES - DailyMed (FDA Monograph)
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Frequently Asked Questions (FAQ)

Common questions about Нитролонг (FAQ)


Q: Is Nitrolong the same as Nitroglycerin, or are they different drugs?

A: Nitrolong is a recognized brand name for a medication that contains the active ingredient nitroglycerin (glyceryl trinitrate). Both terms refer to the same core compound, which is classified as an organic nitrate. The main difference lies in the specific pharmaceutical form that is marketed under the Nitrolong brand.


Q: What are the main differences between Nitrolong and other nitrates?

A: The primary distinction, as described in official product information, is that Nitrolong is typically supplied as a controlled-release (or modified-release) tablet or capsule. This formulation is designed to release the active ingredient slowly over several hours, providing sustained prophylactic protection against symptoms, unlike immediate-release forms.


Q: Are Nitrolong tablets meant to be swallowed whole or dissolved?

A: Official instructions specify that the controlled-release unit must be swallowed whole and must not be chewed or crushed. This requirement is crucial for maintaining the integrity of the controlled-release mechanism, which ensures the medicine is released slowly over time.


Q: Should Nitrolong be taken every day, or only when chest pain occurs?

A: The medicine is officially defined as a prophylactic agent, meaning its purpose is to prevent and manage symptoms over time. For this reason, official instructions state that the drug is not indicated for aborting acute episodes of chest pain, which require a separate type of fast-acting nitrate.


Q: How quickly does Nitrolong begin to work?

A: According to the clinical data from studies on the extended-release formulation, the anti-anginal activity is typically documented to be present about one hour after ingestion. Due to its slow-release design, it is not fast-acting and is not indicated for immediate symptom relief.


Q: What is the maximum duration of action for Nitrolong?

A: Based on studies of the extended-release formulation, the maximal achievable daily duration of the anti-anginal effect is reported to be about 12 hours. This duration aligns with the drug's design goal of providing sustained protection.


Q: What should be done if a dose of Nitrolong is missed?

A: Official administration information often describes the general approach for a missed dose: if a dose is missed, it is typically taken as soon as possible, but if it is almost time for the next scheduled dose, the missed dose is usually skipped. This measure is recommended to help patients avoid taking double or extra doses.


Q: How can a patient tell that Nitrolong is working as intended?

A: Clinical trials explored the effectiveness of the drug by monitoring two key outcomes. These included documented differences in the weekly frequency of angina episodes and the total duration of exercise performed before symptoms appeared during specific functional tests.


Q: Can Nitrolong be taken if a patient has liver problems?

A: Regulatory documents indicate that use requires caution and monitoring in patients with impaired liver function. The prescribing information notes that specific physiological conditions, including impaired liver function, may require careful assessment by a healthcare professional.


Q: Are there official guidelines about driving while taking Nitrolong?

A: Official safety information notes that the medicine may cause side effects like dizziness and hypotension (low blood pressure). The necessity to refrain from driving or operating machinery is described if these symptoms occur, until the individual knows how the product affects these abilities.


Q: Does Nitrolong affect physical endurance?

A: Research evidence studied the medicine's effect by monitoring the total duration of exercise performed before symptoms appeared in patients undergoing specialized functional testing. The drug's influence on physical capability is therefore a documented topic of clinical research.


Q: Is there a risk of symptom exacerbation if Nitrolong is stopped abruptly?

A: Official instructions require the dosage to be reduced gradually over several days when long-term treatment is concluded. This instruction is a requirement for discontinuation protocols to avoid a potential exacerbation of symptoms, which is a documented risk when the medication is stopped suddenly.


Q: Why does Nitrolong’s effect last longer than fast-acting Nitroglycerin?

A: The longer duration of action is a result of the tablet's pharmaceutical design. It is formulated as a controlled-release unit, which is specifically engineered to slowly release the active ingredient into the body over several hours, ensuring sustained protection.


Q: Can Nitrolong interact with herbs or dietary supplements?

A: Authoritative sources note that certain dietary supplements and herbs (such as Hawthorn, Garlic, or L-arginine) may potentiate the hypotensive effect. Official labeling typically highlights the importance of discussing all concurrent medications and supplements with a prescriber.


Q: Is there a difference in effect between different Nitrolong dosages?

A: Regulatory documents state that dosing is individualized and may be initiated at lower available strengths. This indicates that the dosage can be adjusted by the prescriber to achieve an adequate therapeutic response while also managing the occurrence of side effects.


Q: Can Nitrolong help with pain other than chest pain?

A: Official labeling and indications define the product’s use strictly for the prevention and management of chest pain (angina pectoris) caused by coronary artery disease. Use for other types of pain is not addressed in the drug’s regulatory documents.


Q: Where can one find the official prescribing information or patient instructions for Nitrolong?

A: Official drug information, such as the Summary of Product Characteristics (SmPC) or the FDA Prescribing Information (DailyMed), is published and available through government drug agency websites. These sources contain the detailed regulatory data on the medicine.


Q: Is there a risk of methemoglobinemia from Nitrolong?

A: Methemoglobinemia is documented in official labeling as a rare, but clinically important, serious adverse reaction. This condition involves changes in the blood's ability to carry oxygen.


Q: What information is available regarding dizziness after taking Nitrolong?

A: Since dizziness and lightheadedness upon standing are listed as common side effects, official safety information documents the necessity for patients to be seated when taking the medication and to use caution when returning to a standing position. This precaution is described to help prevent falls or injuries.


Q: Why does the instruction sheet mention that the drug may cause facial flushing?

A: The medicine is a potent vasodilator, meaning it causes the relaxation and widening of blood vessel walls, which is its intended mechanism of action. The associated side effect of flushing (reddening of the skin) is documented in official sources as a physical manifestation of this powerful vasodilatory action.

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How should Нитролонг be stored and disposed of?

Official Storage and Disposal Requirements

Storage and disposal instructions for Нитролонг (Nitroglycerin) are based strictly on regulatory prescribing information and official labeling to maintain product stability and ensure safety.

Storage Conditions

Item Requirement
Temperature Store at Controlled Room Temperature (20 C to 25 C), with excursions permitted up to 30 C.
Environmental Mandatory to protect from moisture and light. The product must not be frozen or exposed to excess heat.
Container Rule Must be kept in the original container and be tightly capped after each use; this action is required to prevent the loss of tablet potency.

Disposal and Child Safety

All regulatory labels mandate that the medication must be stored out of the sight and reach of children.

Unused or expired product must be disposed of in accordance with local and national regulations for pharmaceutical waste. Official instructions prohibit disposing of this medication in household trash or flushing it down a toilet or drain.

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

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