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Herten

Active Ingredient:
Enalapril Maleate
Origin:
EU

Herten (Enalapril Maleate)

Herten is a prescription medication that contains the active ingredient Enalapril Maleate. It is supplied as an oral tablet (strength not specified) and belongs to the ACE inhibitor class used to manage cardiovascular conditions. The drug works by interfering with the renin‑angiotensin‑aldosterone system, helping to lower blood pressure and reduce the workload on the heart. Herten is marketed within the European Union and is available only with a physician’s prescription.

Manufacturer / TM Owner

Industria Química Y Farmaceútica Vir, S.A.

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Indications & Clinical Uses

Herten (Enalapril Maleate) is indicated for several cardiovascular conditions where reduction of blood pressure or cardiac workload is desired.

  • Hypertension (essential or secondary) requiring long‑term blood pressure control.
  • Heart failure with reduced ejection fraction to improve symptoms and survival.
  • Asymptomatic left ventricular dysfunction to delay progression to overt heart failure.
  • Post‑myocardial infarction to reduce the risk of subsequent cardiovascular events.
  • Diabetic nephropathy (off‑label) where ACE inhibition can slow renal decline.

How It Works

  • Enalapril is a prodrug that is converted to enalaprilat, a potent inhibitor of angiotensin‑converting enzyme (ACE). By blocking ACE, it prevents the conversion of angiotensin I to the vasoconstrictor angiotensin II, leading to vasodilation, reduced aldosterone secretion, and decreased sodium and water retention. The resulting decline in systemic vascular resistance and blood volume lowers arterial pressure and eases cardiac workload.

Side Effects

Like other ACE inhibitors, Herten may cause a range of adverse reactions, from mild and transient to rare but serious events.

Common

  • Persistent dry cough.
  • Dizziness or light‑headedness.
  • Elevated blood potassium (hyperkalaemia).

Serious

  • Angioedema involving the face, lips, tongue, or airway.
  • Severe hypotension causing fainting.
  • Acute kidney injury or rapid decline in renal function.

Precautions & Warnings

Before initiating Herten, clinicians should evaluate patient history and monitor specific parameters to minimize risk.

  • Assess renal function and serum electrolytes prior to treatment and periodically thereafter.
  • Use cautiously in patients with a history of angioedema or hereditary angioedema.
  • Avoid in pregnancy; ACE inhibitors are contraindicated during the second and third trimesters.
  • Monitor blood pressure closely during the first weeks to detect excessive hypotension.
  • Adjust dose or discontinue if significant hyperkalaemia or worsening renal function occurs.
  • Consider reduced dosing in elderly patients or those with low body weight.

Avoid Interactions

Herten can interact with several medications, altering its efficacy or increasing the risk of adverse events.

Avoid

  • Potassium‑sparing diuretics or supplements that may cause hyperkalaemia.
  • Concomitant use of aliskiren in patients with diabetes or renal impairment.
  • Other ACE inhibitors or angiotensin receptor blockers (dual blockade).

Use with caution

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs) that may reduce antihypertensive effect and affect renal function.
  • Lithium, as ACE inhibition can increase lithium levels.
  • Diuretics, especially thiazides, which may enhance hypotensive response.
  • Certain antibiotics (e.g., trimethoprim‑sulfamethoxazole) that affect potassium balance.

Frequently Asked Questions

Herten is a prescription drug marketed in the EU that contains the active ingredient Enalapril Maleate, an ACE inhibitor used to treat cardiovascular conditions.

Herten is converted in the body to enalaprilat, which blocks the angiotensin‑converting enzyme, reducing formation of angiotensin II and decreasing vasoconstriction and aldosterone‑mediated fluid retention, resulting in lower blood pressure.

Herten is commonly prescribed for hypertension, heart failure with reduced ejection fraction, asymptomatic left ventricular dysfunction, and after myocardial infarction to lower the risk of further cardiovascular events.

The most frequent side effects include a persistent dry cough, dizziness or light‑headedness, and elevated blood potassium levels (hyperkalaemia).

Patients should seek immediate medical attention if they develop swelling of the face, lips, tongue, or throat (angioedema), severe dizziness leading to fainting, or signs of acute kidney injury such as reduced urine output.

Yes, renal function and serum electrolytes should be assessed before starting Herten and monitored regularly, as the drug can affect kidney performance and potassium balance.

Herten, like other ACE inhibitors, is contraindicated during the second and third trimesters of pregnancy and should be avoided unless clearly needed; safety during breastfeeding has not been established.

Medications that should be avoided include potassium‑sparing diuretics, aliskiren in patients with diabetes or renal impairment, and the simultaneous use of other ACE inhibitors or angiotensin receptor blockers.

Potassium‑containing supplements can raise serum potassium levels when taken with Herten, increasing the risk of hyperkalaemia; patients should use such supplements only under medical supervision.

Regular monitoring of blood pressure, renal function (creatinine, eGFR), and serum electrolytes, especially potassium, is recommended during treatment with Herten.

Elderly patients or those with low body weight may require a lower starting dose and careful titration to reduce the risk of hypotension and renal side effects.

NSAIDs can diminish the antihypertensive effect of Herten and may worsen renal function; they should be used with caution and renal function should be monitored.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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