Product image of Licolos Plus (Losartan Potassium, Hydrochlorothiazide) supplied by GNH India

Licolos Plus

Active Ingredient:
Losartan Potassium, Hydrochlorothiazide
Origin:
EU

Licolos Plus (Losartan Potassium, Hydrochlorothiazide)

Losartan potassium, the active ingredient in Licolos Plus, is an angiotensin II receptor blocker presented as an oral tablet for systemic use. It is combined with hydrochlorothiazide, a thiazide diuretic, to treat hypertension in adult patients.

GNH India supplies Licolos Plus as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Laboratorios Liconsa, S.A.

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Indications & Clinical Uses

Licolos Plus is an antihypertensive combination that lowers blood pressure by targeting the renin‑angiotensin system and promoting diuresis.

  • Hypertension: provides effective reduction of systolic and diastolic blood pressure.
  • Hypertension with volume overload: adds diuretic action to improve control in patients retaining fluid.
  • Hypertension in diabetic patients: helps protect renal function while managing blood pressure.

How It Works

  • Losartan potassium selectively blocks the AT1 angiotensin II receptor, preventing vasoconstriction and aldosterone release. Hydrochlorothiazide inhibits sodium‑chloride reabsorption in the distal convoluted tubule, increasing urinary excretion of water and electrolytes. The combined actions reduce peripheral vascular resistance and plasma volume, resulting in lowered arterial pressure.

Side Effects

Adverse reactions may occur with any antihypertensive therapy.

Common Side Effects

  • Dizziness or light‑headedness, especially after the first dose.
  • Headache.
  • Fatigue or weakness.
  • Increased urination.
  • Electrolyte disturbances such as low potassium.
  • Mild gastrointestinal upset.

Serious or Rare Side Effects

  • Severe hypotension.
  • Acute kidney injury.
  • Hyperkalemia.
  • Allergic reactions including rash or angioedema.
  • Liver enzyme elevations.
  • Blood dyscrasias such as agranulocytosis.

Precautions & Warnings

Before initiating therapy, consider patient‑specific factors and monitor appropriately.

  • Pregnancy: avoid use; classified as Category D due to fetal risk.
  • Renal impairment: assess kidney function and adjust dose if needed.
  • Hepatic disease: use with caution; monitor liver enzymes.
  • Electrolyte balance: check serum potassium and sodium regularly.
  • Concomitant potassium‑sparing agents: increase risk of hyperkalemia.
  • Store at ambient temperature: keep below 25°C, in the original container, protected from moisture and light.

Avoid Interactions

Drug interactions can modify the efficacy or safety of the combination.

Major Interactions (Avoid)

  • Aliskiren in patients with diabetes or renal impairment: risk of severe hypotension and renal dysfunction.
  • Potassium supplements or potassium‑sparing diuretics: may cause dangerous hyperkalemia.
  • NSAIDs (e.g., ibuprofen, naproxen): can blunt antihypertensive effect and worsen renal function.

Moderate Interactions (Monitor Closely)

  • Lithium: increased lithium levels, monitor for toxicity.
  • Antidiabetic agents: may require dose adjustment due to enhanced glucose lowering.
  • Other antihypertensives (e.g., ACE inhibitors, beta‑blockers): monitor blood pressure for additive effects.
  • CYP2C9 inhibitors (e.g., fluconazole): may raise losartan levels.
  • Thiazide‑sparing diuretics: monitor electrolytes for imbalance.

Frequently Asked Questions

Licolos Plus is an oral antihypertensive medication that combines losartan potassium, an angiotensin II receptor blocker, with hydrochlorothiazide, a thiazide diuretic. The product is prescribed to lower high blood pressure, especially in patients who need both vasodilation and fluid removal to achieve optimal control.

Losartan potassium selectively blocks the AT1 receptors for angiotensin II, preventing the hormone from causing blood vessels to narrow and reducing aldosterone secretion. This leads to vasodilation and decreased blood volume, which together lower arterial pressure.

The specific dose of Licolos Plus is determined by the prescribing clinician based on the patient’s blood pressure, renal function, and overall health status. Healthcare professionals tailor the regimen to achieve target blood pressure while minimizing side effects.

Licolos Plus is classified as Pregnancy Category D, indicating evidence of fetal risk. It should be avoided during pregnancy, especially in the second and third trimesters. Breastfeeding is not recommended because the drug can be excreted in milk and may affect the infant.

To request Licolos Plus, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details, and any necessary import documentation.

Compared with single‑component agents, Licolos Plus offers the convenience of two mechanisms in one tablet: an ARB for vasodilation and a thiazide diuretic for volume reduction. This can improve adherence and provide more consistent blood‑pressure control than using either component alone.

Licolos Plus tablets should be stored at ambient temperature, below 25 °C, in the original packaging to protect them from moisture and light. Keep the container tightly closed and out of reach of children.

Licolos Plus is taken orally, usually once daily, with or without food, as directed by a healthcare professional. Swallow the tablet whole with a full glass of water; do not crush or chew it unless specifically instructed.

Serious risks include severe hypotension, acute kidney injury, hyperkalemia, and rare allergic reactions such as angioedema. Patients should be monitored for sudden drops in blood pressure, changes in renal function, and any signs of an allergic response.

Licolos Plus should be avoided in patients with known hypersensitivity to losartan, hydrochlorothiazide, or any excipients, as well as in pregnant women (Category D). Caution is also advised for individuals with severe renal impairment, hepatic disease, or electrolyte disturbances unless a physician determines it is appropriate.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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