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Cardiotan H

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Cardiotan H

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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.

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Overview of Cardiotan H

Quick Facts

Property Description
Active Ingredient Valsartan, Hydrochlorothiazide
Form Tablet (Oral Dosage Form)
Pharmacological Class Antihypertensive Combination Therapy (ARB + Thiazide Diuretic)
Common Use Management of high blood pressure (Hypertension)
Origin Synthetic
Prescription Status Prescription-Only Medicine (POM)

What is Cardiotan H and its Pharmacological Classification?

Cardiotan H is a synthetic prescription medicine defined as an Antihypertensive Combination Therapy, used for the foundational management of high blood pressure. It is specifically a Fixed-Dose Combination (FDC) product, meaning it contains two distinct active ingredients in a single Oral Dosage Form (tablet).

This medication belongs to two complementary pharmacological classes: an Angiotensin II Receptor Blocker (ARB), which is Valsartan, and a Thiazide Diuretic, which is Hydrochlorothiazide (HCTZ). The pairing of these two agents in one preparation provides a combined therapeutic strategy. This Dual-Mechanism approach is clinically recognized for producing a more comprehensive and sustained reduction in pressure compared to using either agent individually, serving as a pillar of long-term blood pressure control.


The Dual Components and General Therapeutic Purpose

The purpose of Cardiotan H is to achieve effective management of Hypertension by utilizing two separate pressure-lowering mechanisms simultaneously. Valsartan works primarily to relax and widen blood vessels (Vasodilation), while Hydrochlorothiazide acts on the kidneys to promote the removal of excess salt and water, resulting in Volume Depletion.

The combination of agents from these two classes, ARB and thiazide diuretic, is a recognized method for achieving a potent synergistic effect on blood pressure control. By acting on both vascular resistance and fluid volume, the medication provides a foundational framework for reducing the sustained strain associated with high blood pressure, which is essential for minimizing overall Cardiovascular Risk Reduction. A typical use scenario involves Cardiotan H being prescribed when monotherapy with a single antihypertensive agent proves insufficient to achieve the target blood pressure goal.


The Fixed-Dose Combination (FDC) Structure

Cardiotan H is structurally defined as a single tablet containing both the ARB and the Thiazide Diuretic in a Solid Oral Matrix. This FDC structure simplifies the administration process for adult patients requiring combination therapy.

The integration of Valsartan and Hydrochlorothiazide into a single unit eliminates the need for managing two separate preparations. This structural efficiency is a key benefit, supporting consistent adherence to the prescribed antihypertensive regimen by streamlining the daily intake of both necessary medications.

Regulatory References

  1. NIH DrugBank Valsartan/Hydrochlorothiazide
  2. Valsartan/Hydrochlorothiazide FDA Drug Label
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What side effects are possible with Cardiotan H?

Possible side effects and safety information

The official safety profile for Cardiotan H (Valsartan/Hydrochlorothiazide) classifies possible adverse reactions based on their documented frequency in clinical use and within defined physiological categories.

Adverse reactions are grouped by System-Organ Class (SOC), including effects on the Nervous System (e.g., dizziness, headache), Vascular System (e.g., hypotension), Gastrointestinal System (e.g., nausea, diarrhea), and Metabolism and Nutrition (e.g., electrolyte imbalance).

Reactions are categorized using the standard regulatory framework:

Classification Examples of Documented Effects
Common Dizziness, Fatigue, Hypotension, Nasopharyngitis
Uncommon Vertigo, Cough, Abdominal discomfort, Asthenia
Not Known Angioedema, Severe changes in renal function

The safety profile includes specific documented Serious Adverse Reactions, such as the potential for Angioedema (swelling of the face, lips, or throat) and Acute Renal Failure, which are considered rare but significant risks. Marked shifts in Electrolyte Levels (e.g., Hyponatremia) are also documented safety concerns.

Population-Specific Safety Considerations are defined in official labels. The medicine is generally Contraindicated in the second and third trimesters of pregnancy due to potential fetal harm. Specific regulatory caution is noted for patients with pre-existing Renal Impairment or Hepatic Impairment.

Furthermore, official safety information notes that reactions such as Dizziness and Hypotension are documented as being more frequently observed during the initial phases of treatment, reflecting a time-related safety pattern documented in regulatory texts. This information establishes the boundaries and specific risks associated with the medicine's use.

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Overdose and Emergency Response

Overdose and When to Seek Help

Official regulatory documents define the overdose profile for Cardiotan H (Valsartan/Hydrochlorothiazide) based on the combined acute effects of its two active components.

Overdose Scope Regulatory Documentation
Documented overdose presentations The most likely manifestations are Excessive Hypotension, which may lead to Dizziness or Syncope. Additionally, severe Fluid and Electrolyte Depletion is documented, resulting in Dehydration.
Physiological systems affected (as stated in label) The Cardiovascular System (Hypotension, Arrhythmias) and Electrolyte/Metabolic System (Hypokalemia, Hyponatremia) are primarily affected.
Population-specific overdose notes (if applicable) Overdose risks are specifically noted for patients with Hepatic Impairment, where fluid changes may precipitate Hepatic Coma. Patients concurrently receiving digitalis are also at risk for accentuated cardiac arrhythmias due to hypokalemia.
Emergency-response statements (as written in official documents) Management is defined as employing Symptomatic and Supportive Measures. If excessive hypotension occurs, the patient must be placed in the Supine Position, and an Intravenous Infusion of Normal Saline may be required.

When immediate medical help is required (label-derived phrasing only):

Urgent medical attention is required when manifestations such as Excessive Hypotension, signs of severe Dehydration, or Electrolyte Imbalance are suspected. The immediate goal is the correction of Hypotension, Dehydration, and the documented Electrolyte Depletion by established procedures. Though procedures like Gastric Lavage may be described, the valsartan component is not removed by dialysis, and no specific antidote is known.

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Therapeutic Uses of Cardiotan H

The purpose of Cardiotan H is to provide comprehensive, long-term therapeutic support for adult patients diagnosed with Essential High Blood Pressure (Hypertension). This medication is part of a foundational strategy to address the chronic, silent condition of elevated arterial pressure. Effective blood pressure management is considered relevant for addressing the risk of serious cardiovascular complications.

Sustained Control and Risk Management

Cardiotan H is commonly used to treat the persistent condition of high blood pressure. It addresses the Systemic Vascular Overload, which is the chronic, harmful force exerted on the blood vessels, and contributes to the management of sustained arterial pressure. This supports general well-being by contributing to the stability of elevated readings. This therapeutic approach is primarily relevant for patients requiring a dual strategy to support consistent pressure management over time.

Prevention of Long-Term Vascular Complications

The ultimate goal of this treatment assists in addressing the Future Vascular Complication Risk. By consistently achieving and maintaining a controlled blood pressure level, the medication may assist with supporting functional stability of vital organs. This approach is applied in addressing the risk of severe events such as stroke and heart attack, contributing to easing the overall symptom load.

Quick Fact: Management of Arterial Pressure Feature Benefit Context
Primary Indication Essential High Blood Pressure
Use Scenario Used when single-agent treatment is insufficient
Main Benefit Assists in addressing Future Vascular Complication Risk
Patient Context Adults requiring dual antihypertensive agents

Regulatory References

  1. FDA DailyMed Label for Valsartan and Hydrochlorothiazide
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Eligibility and Restrictions for Use

Cardiotan H is officially approved for use in adult patients whose high blood pressure is not adequately controlled by single-agent therapy. However, official regulatory labeling strictly defines several populations who must not use the medicine.

Absolute Contraindications

The medication is contraindicated in patients with anuria (inability to urinate), severe renal impairment (Creatinine Clearance leq 30 mL/min), or known hypersensitivity to its components or to sulfonamide-derived drugs. Use is strictly forbidden during pregnancy (especially the second and third trimesters) and is to be avoided during breastfeeding. Furthermore, it is contraindicated for diabetic patients who are simultaneously taking aliskiren.

Restrictions and Limitations

Use in pediatric patients (under 18 years) is not recommended because safety and efficacy have not been established. The medicine is not recommended for patients with severe hepatic impairment (severe liver dysfunction). Individuals with specific conditions, such as primary hyperaldosteronism or uncorrected volume depletion, should not be treated or require correction before administration. Caution is also advised for use in older adults and patients with conditions like Systemic Lupus Erytematosus.

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What should I know about interactions with other medicines?

Interactions with other medicines and products

Cardiotan H (Valsartan/Hydrochlorothiazide) has documented interaction patterns that primarily involve effects on fluid balance, serum electrolytes, and drug exposure, as described in official government regulatory labels.


Interaction-Related Restrictions

  • Contraindicated Combination: Co-administration with Aliskiren is formally contraindicated in patients with diagnosed diabetes mellitus or those with moderate to severe renal impairment. This restriction is due to the risks associated with dual blockade of the Renin-Angiotensin System (RAS).
  • Potassium Agents: Co-administration with Potassium-sparing diuretics or Potassium supplements is generally not recommended due to the increased, additive risk of hyperkalemia.

Pharmacodynamic and Exposure Interactions

  • NSAIDs and Renal Function: Non-Steroidal Anti-Inflammatory Drugs (NSAIDs), including COX-2 selective inhibitors, may reduce the medicine’s antihypertensive effect and increase the risk of renal function changes.
  • Lithium: Co-use with Lithium can increase serum lithium concentrations and the risk of toxicity because the clearance of lithium is reduced.
  • Transporters: The Valsartan component is a substrate of the hepatic uptake transporter OATP1B1; inhibitors of this transporter may therefore increase the drug's systemic exposure.
  • Other Agents: Alcohol may potentiate the effect of orthostatic hypotension. Antidiabetic drugs may require a dosage adjustment, as thiazides can alter glucose tolerance.

Timing-Based Separation Rule

  • A key pharmacokinetic interaction requires spacing the doses: The hydrochlorothiazide component's absorption is reduced by Cholestyramine or Colestipol. Therefore, the medicine must be administered at least 4 hours before or 4 to 6 hours after the administration of these ion-exchange resins.
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Mechanism of Action

Cardiotan H is a combination pharmaceutical product containing two distinct agents: an angiotensin II receptor blocker (ARB) and a thiazide diuretic.

The ARB component, telmisartan, functions as a specific antagonist of the Angiotensin II type 1 ( AT1) receptors primarily located on vascular smooth muscle and adrenal cortical cells. By competitively binding to the AT1 receptor, telmisartan prevents the interaction of endogenous angiotensin II, thereby blocking the Gq protein-coupled signaling cascade. This inhibition suppresses the intracellular calcium mobilization and the downstream activation of vasoconstrictive pathways, leading to smooth muscle relaxation and systemic vasodilation. Additionally, AT1 receptor blockade reduces angiotensin II-mediated aldosterone release, modulating renal sodium and water handling.

The diuretic component, hydrochlorothiazide, acts in the distal convoluted tubule of the nephron as a reversible inhibitor of the sodium-chloride cotransporter ( NCC). Blocking NCC reduces the reabsorption of sodium and chloride ions from the tubular fluid. The resulting increase in Na^+ and water delivery to the collecting duct leads to an osmotic diuresis and natriuresis. This cellular-level transport modification results in a sustained reduction of extracellular fluid volume and overall plasma volume.

Combined, these distinct actions lead to a system-level physiological consequence of decreased peripheral vascular resistance, achieved through two separate mechanisms: direct vascular relaxation and plasma volume reduction.

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Dosage and Administration Information

Cardiotan H is a fixed-dose combination medicine strictly intended for oral administration as a film-coated tablet. It is used for the long-term management of chronic essential hypertension. The tablet must be swallowed whole and should not be crushed or split, and may be taken once daily either with or without food.


Standardized Dosing Protocol

The administration of Cardiotan H follows a defined protocol for adult patients. The usual starting dose is 160 mg of Valsartan combined with 12.5 mg of Hydrochlorothiazide, taken once daily. The dosage is not static and may be titrated (adjusted) by a healthcare provider after a period of 1 to 2 weeks of therapy to achieve the optimal blood pressure goal. The maximum recommended daily dose is 320 mg/25 mg of the combined agents.

Procedural and Population Constraints

If a dose is missed, the procedure is to skip the forgotten dose and resume the regular dosing schedule the following day; doubling the dose is not the approved instruction. The use of Cardiotan H is constrained in specific populations. It is not recommended for pediatric patients under 18 years of age. Furthermore, it is not used in patients with severe renal impairment (creatinine clearance less than 30 mL/min). In patients with mild-to-moderate hepatic impairment, caution is applied, and the Valsartan component dose should not exceed 80 mg. These instructions define the standardized approach to using the medicine.

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Recent Clinical Evidence

Research Evidence / Overview of Studies for Cardiotan H

Evidence for Use in Managing Essential High Blood Pressure

The research base that has explored Cardiotan H primarily includes Randomized Controlled Trials (RCTs). These short-term studies were typically conducted over 8 to 12 weeks and were designed to explore the combination of Valsartan and Hydrochlorothiazide in adult patients diagnosed with essential high blood pressure. In these trials, researchers compared the fixed-dose combination (FDC) against a placebo and against the individual drugs taken alone (monotherapy). The main objective of these studies was to measure changes from initial levels in sitting systolic and diastolic blood pressure.

Research explored the patterns of blood pressure change associated with combining the two active ingredients, compared to patterns seen with monotherapy. Studies reported patterns where differences in blood pressure readings were observed among participants taking the fixed-dose combination compared to those taking the monotherapies. Findings suggest that the combination of the two drugs was studied to assess whether the measured changes differed from patterns seen with monotherapy. Studies also monitored the proportion of participants who achieved predefined blood pressure goals; results describe the patterns observed in the participants taking the combination.

Comparison of the Combination Therapy in Clinical Trials

This area details how the fixed-dose combination was evaluated against other active treatments or monotherapies. It explains the design of the comparative trials evaluated by regulators for this condition. This research examined how the FDC was associated with measured outcomes compared to other single agents or combination regimens. Findings describe the specific context under which the combination was evaluated.

This comparative research contributes to the broader evidence landscape by showing how the FDC operates within the context of other standard antihypertensive strategies. Research describes changes measured during the study period, detailing the combination's findings compared with other treatments explored in the trials.

Long-Term Research and Major Cardiovascular Outcomes

While short-term RCTs established the effects on blood pressure, more complex, long-term research is required to evaluate outcomes related to functional imbalance, such as the prevention of major cardiovascular events. Dedicated, multi-year studies focusing solely on the fixed-dose combination itself are limited. Instead, long-term insights are primarily drawn from larger, extended outcome trials that focused on the regimen involving the Valsartan component.

Research Gaps and Uncertainties

Despite the existence of multiple RCTs, certain aspects of Cardiotan H research remain open to further investigation. There is limited information for long-term outcomes specifically derived from studies where the fixed-dose combination was the primary intervention over the entire duration of follow-up. Data for certain patient groups, such as those with highly specific comorbidities or severe kidney or liver impairment, are limited. Results apply only to the populations studied, and data are still emerging regarding extrapolation to populations not well-represented in the core trials.

Key Studies & References

  1. Valsartan and Hydrochlorothiazide tablets (DIOVAN HCT) - Clinical Pharmacology and Clinical Studies Summary. U.S. National Library of Medicine, DailyMed.
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Frequently Asked Questions (FAQ)

Common questions about Cardiotan H (FAQ)


Q: Is Cardiotan H the same as Telmisartan, or is it a different drug?

Cardiotan H is a combination medicine containing two active ingredients: valsartan and hydrochlorothiazide (HCTZ). Valsartan is an Angiotensin II Receptor Blocker (ARB). Telmisartan is a different medication that also belongs to the ARB class, but it is not the ARB component found in Cardiotan H.

Q: How long does it take for common side effects of Cardiotan H to go away?

Official product information does not specify the exact time frame for side effects to resolve. However, common effects like dizziness and low blood pressure (hypotension) are documented as occurring more frequently during the initial phases of treatment. The dosage is typically evaluated by a healthcare provider after the initial one to two weeks of therapy.

Q: What are the signs of a serious, but rare, allergic reaction to Cardiotan H?

Serious adverse reactions documented in regulatory sources include angioedema, which involves sudden swelling of the face, lips, throat, or tongue. This condition can potentially cause difficulty breathing. Official labeling notes that some patients who experience this had previously experienced angioedema while taking other blood pressure medications.

Q: Is there a connection between Cardiotan H and changes in blood sugar levels?

Yes, official sources indicate that the hydrochlorothiazide component in the medication may alter glucose tolerance in the body. Because of this known effect, patients with diabetes may require an adjustment of their antidiabetic medication dosage.

Q: Are there any known long-term side effects associated with Cardiotan H?

While dedicated, long-term studies focusing solely on this specific fixed-dose combination are limited, follow-up studies reported that the blood pressure-lowering effects were sustained for up to two years. Postmarketing data includes reports of non-melanoma skin cancer as a potential long-term risk associated with chronic use of hydrochlorothiazide.

Q: How quickly should I expect Cardiotan H to begin lowering my blood pressure?

The full, maximum blood pressure-lowering effect is generally seen after approximately four weeks of continuous treatment. Because of this, the dosage is usually evaluated and adjusted, if necessary, by a healthcare provider after the first one to two weeks of therapy.

Q: What other types of medications should be reviewed with a doctor before starting Cardiotan H?

Several classes of medications are listed as requiring review, including those that increase potassium levels, such as potassium-sparing diuretics and potassium supplements. Also, Non-Steroidal Anti-Inflammatory Drugs (NSAIDs), Lithium, and certain cholesterol-lowering resins are explicitly mentioned as having documented interactions.

Q: What have clinical research studies found regarding the long-term benefits of Cardiotan H?

Controlled trials have demonstrated that achieving and maintaining a lower blood pressure reduces the risk of fatal and nonfatal cardiovascular events, such as strokes and heart attacks. Dedicated controlled trials specifically demonstrating this risk reduction for the combination product are noted as limited in regulatory information.

Q: Does Cardiotan H offer any cardiovascular protection beyond simply controlling blood pressure?

The primary purpose is the management of high blood pressure. By lowering blood pressure, the drug classes in this medicine are associated with reducing the risk of fatal and nonfatal cardiovascular events, including strokes and myocardial infarctions, which is a key component of long-term cardiovascular health.

Q: How does the Valsartan component in Cardiotan H compare to a different class of drugs, like ACE inhibitors?

The Valsartan component belongs to the ARB class, which blocks the effects of Angiotensin II on specific AT1 receptors. This differs from ACE inhibitors (like lisinopril), which block the enzyme that creates Angiotensin II. Unlike ACE inhibitors, Valsartan does not affect bradykinin metabolism.

Q: Why might a doctor choose Cardiotan H over taking a single drug alone?

The combination medicine is typically indicated for patients whose high blood pressure is not adequately controlled on monotherapy (a single medication like an ARB or diuretic). The two agents work by different mechanisms, providing a combined strategy that is often needed to reach blood pressure goals.

Q: What are excipients and are there any common allergens in Cardiotan H tablets?

Excipients are the inactive ingredients used to form the tablet. Due to the hydrochlorothiazide component, the medicine is contraindicated in patients with known hypersensitivity to any of the components or to sulfonamide-derived drugs.

Q: Are there specific blood tests that should be monitored regularly when taking Cardiotan H?

Regulatory guidelines advise that monitoring is necessary for susceptible patients. Specifically, serum electrolytes (such as potassium) and renal function should be periodically monitored to assess the drug's effects on the body's balance and kidney performance.

Q: Can Cardiotan H affect mental focus or cause drowsiness?

Yes, official adverse reaction reports list somnolence (drowsiness), dizziness, and fatigue as effects that have been reported by patients. These types of effects may also temporarily affect mental focus or coordination.

Q: Is it dangerous to stop taking Cardiotan H without medical supervision?

The medication is approved for the long-term management of chronic hypertension. While the labeling does not explicitly detail the specific danger of abrupt cessation, abrupt discontinuation of an antihypertensive regimen may lead to a loss of blood pressure control.

Q: Does Cardiotan H help reduce the chance of heart attack?

Studies of the drug classes show that lowering and controlling high blood pressure reduces the risk of serious cardiovascular events, including myocardial infarctions (heart attacks). This is considered a fundamental benefit achieved by maintaining blood pressure control.

Q: Can Cardiotan H cause muscle or back pain?

Yes, regulatory documentation lists several musculoskeletal issues as adverse reactions observed in clinical trials. These include reported instances of back pain, myalgia (muscle pain), and muscle cramps.

Q: Can Cardiotan H make my skin more sensitive to the sun?

Yes, official product information reports that the hydrochlorothiazide component may cause a reaction called photosensitivity, which is an increased sensitivity to sunlight. In the event of such a skin reaction, the label advises reviewing treatment with a healthcare provider.

Q: Can Cardiotan H cause vision problems or affect my eyes?

Yes, the hydrochlorothiazide component has been associated with specific eye issues. These include reports of visual disturbances, transient blurred vision, and the potential for a serious, rapid onset eye problem called acute angle-closure glaucoma.

Q: How long does the effect of Cardiotan H last after a single dose?

The medicine is typically prescribed to be taken once daily. This dosing schedule is consistent with the drug's established duration of action, which is designed to effectively manage blood pressure over a full 24-hour period.

Q: Are there any common foods or drinks that should be avoided with Cardiotan H?

Official labeling advises caution or avoidance regarding certain items that affect the body's potassium balance. This includes potassium-containing salt substitutes and potassium supplements, as co-administration can increase the risk of high potassium levels (hyperkalemia).

Q: Does the time of day I take Cardiotan H affect how well it works?

The medicine is a once-daily tablet. While it can be taken with or without food, regulatory sources sometimes advise taking the daily dose preferably in the morning to align with the intended therapeutic profile.

Q: Does Cardiotan H affect cholesterol or triglyceride levels?

Yes, regulatory warnings indicate that the hydrochlorothiazide component may cause an increase in serum levels of cholesterol and triglycerides in some patients. This is listed under the medicine's documented metabolic effects.

Q: Is there a generic version of the Cardiotan H combination available?

Yes, the combination of the active ingredients, valsartan and hydrochlorothiazide, is available as a generic medication.

Q: Does using Cardiotan H increase the risk of developing gout?

Yes, the hydrochlorothiazide component may raise the serum uric acid level. Because of this, regulatory information states that the medicine may potentially cause or worsen symptoms of gout in individuals susceptible to the condition.

Q: Why is the drug sometimes prescribed for people who have had a high risk of stroke?

Official evidence from controlled trials shows that reducing high blood pressure is an effective way to lower the risk of fatal and nonfatal cardiovascular events, particularly strokes and heart attacks. The medicine is used to achieve this blood pressure control.

Q: What information is available about Cardiotan H and its effect on sleep?

Insomnia (sleeplessness) has been reported as an adverse reaction in clinical trials. Insomnia, like any adverse effect, is information that should be shared with a healthcare provider.

Q: Does the effectiveness of Cardiotan H differ between genders?

Studies have examined the medicine's effects across different groups. Official regulatory labeling indicates that the antihypertensive effect of Cardiotan H is reported to be independent of age or gender.

Q: Is Cardiotan H considered an appropriate treatment for heart failure?

The fixed-dose combination (FDC) is indicated for the management of high blood pressure. However, the valsartan component alone is also indicated in some patients for the treatment of heart failure, depending on the individual therapeutic strategy determined by a healthcare provider.

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How should Cardiotan H be stored and disposed of?

Storage and Disposal Requirements

Cardiotan H tablets must be stored at Controlled Room Temperature, which is defined as 20 C to 25 C (68 F to 77 F), with permitted short-term excursions up to 30 C (86 F). The medication must be kept in its original container and the container must remain tightly closed to protect the contents from moisture and direct light.

It is officially required to keep the medicine out of the reach of children. The product must be stored away from excessive heat and must not be frozen. Do not keep expired or unused medicine. For disposal, unused or expired Cardiotan H should be taken to a government-approved drug take-back program or disposed of according to the specific guidance of local regulations.

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

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