Cardismo

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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 Cardismo

Property Description
Active Ingredient Isosorbide Mononitrate
Form Oral Tablets (Standard and Prolonged-Release)
Pharmacological Class Organic Nitrate, Vasodilator
General Purpose Reduction of cardiac workload (Preload and Afterload)
Origin Synthetic, Single-ingredient product

What is Cardismo and What Type of Medicine is It?

Cardismo is a brand-name medication containing the active chemical substance Isosorbide Mononitrate (Isosorbide 5-mononitrate). This compound is classified as a synthetic, single-ingredient product belonging to the Organic Nitrate group and is primarily categorized as a systemic Vasodilator. It is designated as a prescription-only medicine (Rx) used for the prophylactic management of the cardiovascular system. Isosorbide Mononitrate is an Antianginal agent, and this formulation is a long-acting organic nitrate used for proactive management.

Why is Isosorbide Mononitrate Classified as an Antianginal Agent?

Isosorbide Mononitrate is grouped within the antianginal category because its fundamental physiological action is to reduce the workload and oxygen demand of the heart muscle. This effect is achieved through widespread Vasodilation, which relaxes the smooth muscle within blood vessel walls. This action facilitates peripheral pooling of blood, thereby decreasing the volume of blood returning to the heart (known as Preload reduction), and causes a moderate widening of the arteries (known as Afterload reduction). This two-fold action reduces the burden on the heart, allowing it to function more efficiently.

What are the Available Forms of Cardismo?

Cardismo is supplied as an Oral formulation in the form of Tablets, intended for systemic absorption via the digestive tract. The drug is known for offering both a standard-release preparation and a specialized prolonged-release format. The prolonged-release tablet is chemically engineered to release the Isosorbide Mononitrate active ingredient gradually over an extended period. This design is crucial for sustained systemic delivery, which is a key consideration for agents used in long-term prophylactic regimens.

Regulatory References

  1. European Medicines Agency
  2. European Public Assessment Reports (EPAR)

What side effects are possible with Cardismo?

Possible Side Effects and Safety Information

The safety profile for Isosorbide Mononitrate (Cardismo) is structured by government regulatory agencies using frequency categories and System-Organ-Class (SOC) groupings. The majority of documented adverse reactions are pharmacologically linked to the drug’s vasodilatory action.


Frequency-Classified Adverse Reactions

Side effects are categorized based on their official reported occurrence rates:

  • Very Common (1/10): Headache, which is often described as throbbing.
  • Common (1/100 to <1/10): Dizziness, Tachycardia (increased heart rate), Hypotension (low blood pressure), Nausea, and Fatigue.
  • Uncommon (1/1,000 to <1/100): Vomiting, Diarrhoea, and Flushing.

These effects primarily affect the Nervous System (e.g., headache) and the Vascular System (e.g., hypotension). Regulatory documents note that the very common headache often diminishes or disappears after the initial 1 to 3 weeks of treatment.


Serious Adverse Reactions and Safety Constraints

The safety profile highlights certain reactions that may be severe. These include Severe Hypotension leading to Syncope (fainting) or, rarely, Acute Circulatory Failure (shock). Aggravation of Angina Pectoris is also documented.

Safety Restrictions define necessary limitations on use. The medication is contraindicated for use in individuals taking Phosphodiesterase Type 5 (PDE5) inhibitors (e.g., sildenafil) or the soluble guanylate cyclase stimulator Riociguat, due to the risk of life-threatening severe hypotension. Caution is advised for older adults due to a potentially higher risk of severe low blood pressure, and for patients with severe hepatic or renal impairment.

Overdose and Emergency Response

The official regulatory documentation for Cardismo (Isosorbide Mononitrate) defines overdose primarily by the resulting severe systemic vasodilation. Documented manifestations include a prompt fall in blood pressure (hypotension), accompanied by tachycardia, a persistent throbbing headache, vertigo, nausea, and vomiting. More serious outcomes may involve syncope (fainting), circulatory failure, convulsions, or a dangerous rise in intracranial pressure.

Urgent medical attention must be sought immediately if an overdose is suspected or if these severe symptoms occur. The required emergency action is symptomatic and supportive treatment, focusing on increasing the central fluid volume through measures such as passive elevation of the patient's legs or intravenous fluid infusion. The use of Epinephrine or other arterial vasoconstrictors is cautioned against, as per official guidance.

A specific, rare, but life-threatening complication documented is Methaemoglobinaemia, which causes a reduction in oxygen-carrying capacity and may lead to cyanosis. For severe cases of this complication, Methylene Blue is the officially specified treatment. Hospital monitoring, including observation for at least twelve hours and continuous monitoring of blood pressure and pulse, is required in the management of overdose situations.

Therapeutic Uses of Cardismo

What Cardismo Treats: Main Uses and Benefits

Isosorbide Mononitrate is primarily used for the long-term prophylactic management of cardiovascular conditions, specifically focusing on chronic stable angina pectoris in patients diagnosed with coronary artery disease (CAD). Its fundamental therapeutic role is commonly used to help reduce the frequency of symptoms that interfere with daily functioning, such as recurrent episodes of chest pain and other manifestations of myocardial ischemia. This makes it relevant when supportive symptom management is appropriate for patients requiring sustained, daily antianginal protection.

The medication is commonly used to help address symptoms related to physical discomfort and systemic imbalance across conditions like chronic stable angina, supporting functional capacity, and as an adjunctive treatment for chronic heart failure. The treatment is centered on supportive relief across conditions characterized by periods of heightened symptoms and focuses instead on continuous disease management. This is why the medication may assist with managing the intensity of episodes.

“The therapy is applied to support the patient during difficult episodes by easing distress and helping to maintain a sense of stability when symptoms are more noticeable.”

The practical patient benefit helps to manage symptoms that interfere with daily functioning and supports maintaining functional stability. The treatment assists with maintaining functional stability and contributes to easing the overall symptom load during symptomatic periods.


Quick Fact: Relief for Recurrent Chest Pain The medication is typically applied in clinical settings that involve recurrent or episodic manifestations of chest discomfort, helping to ease the overall symptom burden associated with chronic cardiac conditions.

Regulatory References

  1. NIH MedlinePlus overview on Isosorbide Mononitrate

Eligibility and Restrictions for Use

Official Eligibility and Contraindications

Cardismo (Isosorbide Mononitrate) is approved for use in adults for the chronic management of their condition. The official regulatory labeling specifies clear restrictions and absolute prohibitions on who must not use this medicine.


Absolute Contraindications

The medicine must not be used in patients with a known hypersensitivity to isosorbide mononitrate or any other nitrates. It is also strictly prohibited in patients with marked low blood pressure (le 90 mm Hg systolic) or acute circulatory failure (shock). Use is contraindicated if the patient is simultaneously taking Phosphodiesterase Type 5 (PDE5) inhibitors (like sildenafil) or the soluble guanylate cyclase stimulator riociguat.


Population and Organ Limitations

  • Pediatric Use: Safety and efficacy have not been established in children.
  • Older Adults: While no routine dosage adjustment is needed, special care may be required due to increased risk of hypotension.
  • Organ Function: Caution is required for patients with severe renal or hepatic impairment.
  • Pregnancy/Lactation: Safety is not established. Use is only recommended if the possible benefits outweigh the hazards.

What should I know about interactions with other medicines?

The official regulatory profile for Cardismo (Isosorbide Mononitrate) defines interaction constraints based on the potential for amplified pharmacological effects and additive vasodilation.

Contraindicated Combinations

Co-administration with Phosphodiesterase-5 (PDE5) inhibitors (including sildenafil, tadalafil, and vardenafil) is formally contraindicated by government regulators. This strict prohibition is due to the risk of severe and potentially life-threatening hypotension or myocardial ischemia resulting from documented pharmacodynamic reinforcement. The same absolute restriction applies to co-administration with the Soluble Guanylate Cyclase (sGC) stimulator riociguat, which also carries a significant risk of severe hypotension.

Documented Additive Effects

Additive vasodilatory effects are documented with other medicinal products. Concurrent use with alcohol (ethanol), other vasodilators, or calcium channel blockers may increase the frequency of symptomatic orthostatic hypotension. Potentiated hypotensive effects are further noted when combined with beta-blockers, ACE inhibitors, neuroleptics, and tricyclic antidepressants. Co-administration with dihydroergotamine may increase its blood level and potentiate its hypertensive effect.

Food Interaction Constraint

For the prolonged-release tablet, official labeling notes that a high-fat, high-calorie meal may decrease the rate of absorption ( T max) without altering the total extent of exposure ( AUC) of Isosorbide Mononitrate. No clinically relevant metabolic or transporter-based interactions that affect the drug’s clearance are cited in the official regulatory profile.

Mechanism of Action

Enzymatic Initiation of the Nitric Oxide Pathway

The mechanism begins with Isosorbide Mononitrate acting as a pro-drug, requiring conversion by the enzyme Aldehyde Dehydrogenase-2 (ALDH-2) within the vascular cells. This enzymatic biotransformation releases the active signaling molecule, Nitric Oxide (NO). This initial molecular action is required to engage the core pathway that regulates blood vessel tone.


The cGMP Signal and Smooth Muscle Relaxation

The released Nitric Oxide (NO) immediately activates its primary molecular target, soluble Guanylate Cyclase (sGC), which synthesizes the second messenger, cyclic Guanosine Monophosphate (cGMP). This cGMP cascade activates protein kinase G (PKG), ultimately causing the vascular smooth muscle to relax.


Systemic Vasodilation and Preload Reduction

The resultant relaxation, or vasodilation, is most pronounced in the systemic veins, causing blood to pool in the peripheral circulation. This action decreases the volume of blood returning to the heart, a key physiological change known as a reduction in preload. By reducing preload and moderately reducing afterload, the mechanism results in a lower myocardial oxygen requirement and a decrease in the physical work load on the heart.

Dosage and Administration Information

How to Use Cardismo

Cardismo (Isosorbide Mononitrate) is an antianginal agent that is strictly intended for long-term prophylactic use and must not be used to treat an acute episode of angina, which requires a fast-acting nitrate. The medication is formulated for oral administration as both standard Immediate-Release (IR) and specialized Extended-Release (ER) tablets.

Dosing and Administration Schedule

All administration schedules are structured around the primary goal of establishing a daily nitrate-free interval (NFI) of approximately 10 to 14 hours to prevent the development of pharmacological tolerance.

Formulation Dosing Schedule Typical Adult Dose Range
Immediate-Release (IR) Twice daily, taken asymmetrically (e.g., 7 hours apart) to maintain the NFI. Starts at 20 mg twice daily.
Extended-Release (ER) Once daily, typically taken in the morning upon arising to facilitate the NFI overnight. Maintenance of 60 to 120 mg once daily.

Procedural Instructions

Tablet Handling: Extended-release tablets must be swallowed whole with fluid and must not be crushed, chewed, or split to preserve the sustained-release mechanism. The medication can be taken with or without food.

Discontinuation and Adjustment: The medication is for long-term therapy and should not be stopped suddenly; the dosage must be tapered gradually to avoid rebound effects. Use in the pediatric population has not been established, and while no routine dose adjustment is mandated for renal or hepatic impairment, special care is noted.

Recent Clinical Evidence

Research Evidence / Overview of Studies for Cardismo

Evidence for Preventing Chronic Stable Angina Pectoris

The main body of research for Cardismo (Isosorbide Mononitrate) focuses on its use, as explored in studies, for the long-term management of chronic stable angina pectoris, which is chest pain caused by coronary artery disease. This research primarily consists of numerous Randomized Controlled Trials (RCTs). These are studies where adult patients were randomly assigned to receive either the medicine or a placebo (a sugar pill), allowing researchers to monitor recorded outcomes in a controlled setting.

The studies monitored a range of outcomes describing perceived discomfort and functional capacity. Researchers examined the reported frequency of anginal attacks that patients experienced and monitored the patient-reported need for acute relief medications. Findings from these trials describe patterns observed in the studies where researchers recorded measurements of symptomatic and functional outcomes during the observed study period compared to the placebo groups.

Primary Study Endpoints: Symptoms and Exercise Capacity

The specific conditions under which the research was conducted focused on the specific outcomes researchers chose to measure and track. Key research endpoints were designed to capture phases of heightened symptom activity, such as the time to onset of chest pain during measured physical exertion. Research provides context but not individual predictions, as study results reflect the specific conditions under which they were conducted.


Evidence as Supportive Treatment for Chronic Heart Failure

Cardismo was also evaluated in research as an adjunctive treatment (a treatment added to an existing regimen) for conditions related to chronic heart failure. This research involved dedicated RCTs, including a large-scale study that specifically examined patients with heart failure who had preserved ejection fraction (HFpEF). Findings in this area have been mixed. One key trial described patterns showing that the medication's use was associated with lower overall physical activity levels in some patients compared to placebo.

Key Research Limitations and Uncertainties

Studies suggest that research for Cardismo has a large body of research regarding the short-term outcomes tracked for anginal symptoms. However, a central focus for researchers is the persistent issue of nitrate tolerance, which was observed in studies and may lead to an attenuation of the measured antianginal effect over time. Other research limitations include the fact that follow-up durations were limited in many pivotal trials, and thus, the impact on long-term survival or preventing serious cardiac events is not characterized by the research findings.

Key Studies & References

  1. Summary Public Assessment Report Isomex (isosorbide mononitrate) - Swedish Medical Products Agency (Generic reference for regulatory context)

Frequently Asked Questions (FAQ)

Common questions about Cardismo (FAQ)


Q: What happens if I miss a dose of Cardismo?

Official product information on Cardismo (Isosorbide Mononitrate) indicates that a missed dose may be taken as soon as it is remembered. However, if it is almost time for the next scheduled dose, it is generally recommended to skip the missed dose and resume the regular schedule. It is also stated that a double dose should not be taken to make up for the one that was missed.


Q: What should I do if I accidentally take too much Cardismo (overdose)?

Regulatory documents indicate that taking too much Cardismo can lead to symptoms related to widespread widening of blood vessels. These effects may include severe low blood pressure (hypotension), a throbbing headache, dizziness, and fainting (syncope). If an overdose is suspected, immediate emergency medical attention should be sought.


Q: Is it safe to take this medicine while pregnant or breastfeeding?

Official labeling states that the safety of Cardismo during pregnancy and breastfeeding has not been established. Use is only recommended if the potential benefits are judged to outweigh any possible risks. Furthermore, it is currently unknown if the active ingredient is passed into human breast milk.


Q: How long does it take for Cardismo's headache side effect to go away?

The headache side effect, which is very common with this type of medicine, is generally temporary. According to the regulatory safety profile, this headache often lessens in severity or disappears entirely after the initial one to three weeks of continuous therapy.


Q: Can Cardismo affect my ability to drive or operate machinery?

Regulatory information advises caution, as this medicine may cause side effects such as dizziness, light-headedness, and low blood pressure (hypotension). Due to these potential effects, the ability to perform tasks that require mental alertness, such as driving or operating machinery, may be temporarily impaired.


Q: Can Cardismo interact with over-the-counter pain relievers like ibuprofen or aspirin?

Official information notes that certain over-the-counter pain relievers, particularly Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) such as ibuprofen, may potentially reduce the medicine’s effectiveness. For temporary relief of the common headache side effect, pain relievers like acetaminophen are often mentioned in regulatory texts.

How should Cardismo be stored and disposed of?

How to Store and Dispose of Cardismo (Isosorbide Mononitrate)

Cardismo tablets must be stored at Controlled Room Temperature, which is generally defined as 15 C to 30 C. The medication must be protected from light and excess moisture and should be stored in a dry location, away from excessive heat. It is a mandatory requirement to keep the tablets in the original, tightly closed container and strictly out of the sight and reach of children.

Disposal

Do not dispose of Cardismo via household waste or by flushing it down a drain. Unused or expired medication must be discarded according to local regulations or through a formal drug take-back program to ensure environmental safety.

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

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