Product image of Paniltri (Hydrochlorothiazide, Ramipril, Amlodipine Besilate) supplied by GNH India

Paniltri

Active Ingredient:
Hydrochlorothiazide, Ramipril, Amlodipine Besilate
Origin:
EU

Paniltri (Hydrochlorothiazide, Ramipril, Amlodipine Besilate)

Hydrochlorothiazide, Ramipril and Amlodipine Besilate, the active ingredients in Paniltri, are a combination antihypertensive presented as oral tablets for systemic use. The fixed‑dose combination lowers elevated blood pressure in adult patients by targeting fluid balance, the renin‑angiotensin system and vascular smooth‑muscle tone.

GNH India supplies Paniltri as a licensed, GDP‑compliant international pharmaceutical supplier, providing quality‑assured products to hospitals, pharmacies and clinics worldwide, with adherence to EU manufacturing standards and robust distribution networks. Our supply chain includes temperature‑controlled logistics where required and comprehensive regulatory documentation for seamless import.

Manufacturer / TM Owner

Laboratório Medinfar - Produtos Farmacêuticos, S.A.

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Indications & Clinical Uses

Paniltri, a fixed‑dose combination antihypertensive, is indicated for the management of elevated blood pressure.

  • Hypertension: provides effective blood pressure reduction in adults with primary hypertension.
  • Resistant hypertension: offers an additional therapeutic option when blood pressure remains uncontrolled on two agents.
  • Hypertension with fluid retention: helps control blood pressure and reduces peripheral edema by combining a diuretic with vasodilators.
  • Hypertension in chronic kidney disease: slows renal function decline by inhibiting the renin‑angiotensin system.

How It Works

  • Hydrochlorothiazide acts on the distal convoluted tubule to inhibit NaCl reabsorption, promoting diuresis. Ramipril blocks the conversion of angiotensin I to angiotensin II, reducing vasoconstriction and aldosterone secretion. Amlodipine Besilate selectively inhibits L‑type calcium channels in vascular smooth muscle, causing arterial dilation. Together these actions decrease plasma volume, systemic vascular resistance and cardiac afterload, resulting in lowered arterial pressure.

Side Effects

Paniltri may cause a range of adverse reactions that vary in frequency and severity.

Common Side Effects

  • Dizziness: sensation of light‑headedness, especially after standing.
  • Headache: mild to moderate pain in the head region.
  • Peripheral edema: swelling of ankles or feet.
  • Cough: dry, persistent throat irritation.
  • Fatigue: feeling unusually tired or weak.
  • Increased urination: more frequent need to void.

Serious or Rare Side Effects

  • Angioedema: rapid swelling of face, lips or throat requiring emergency care.
  • Severe hypotension: marked drop in blood pressure causing faintness.
  • Electrolyte imbalance: especially hyperkalemia or hyponatremia.
  • Acute renal impairment: sudden decline in kidney function.
  • Hepatic dysfunction: abnormal liver enzyme elevations.
  • Pancreatitis: inflammation of the pancreas presenting with abdominal pain.

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety aspects.

  • Blood pressure monitoring: ensure target levels are achieved without excessive drop.
  • Renal function assessment: evaluate serum creatinine and eGFR periodically.
  • Electrolyte surveillance: check potassium and sodium levels, especially with diuretic use.
  • Pregnancy and lactation: avoid use unless clearly indicated, as risks may outweigh benefits.
  • Elderly patients: start at lower doses and monitor for orthostatic symptoms.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Paniltri can interact with other medicines, altering its efficacy or safety.

Major Interactions (Avoid)

  • Aliskiren: combined renin inhibition may cause renal dysfunction.
  • NSAIDs: can blunt antihypertensive effect and increase renal risk.
  • Potassium‑sparing agents or supplements: heightened risk of hyperkalemia.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inhibitors (e.g., clarithromycin): may increase amlodipine concentrations.
  • Other antihypertensives (e.g., beta‑blockers): additive hypotensive effect.
  • Non‑potassium‑sparing diuretics: may exacerbate electrolyte disturbances.

Frequently Asked Questions

Paniltri is a fixed‑dose combination of hydrochlorothiazide, ramipril and amlodipine Besilate indicated for the treatment of hypertension. It is prescribed to lower elevated blood pressure in adult patients, often when monotherapy does not achieve target control.

Hydrochlorothiazide promotes diuresis by inhibiting sodium‑chloride reabsorption in the distal tubule, reducing plasma volume. Ramipril blocks the conversion of angiotensin I to angiotensin II, decreasing vasoconstriction and aldosterone‑mediated sodium retention. Amlodipine relaxes vascular smooth muscle through calcium‑channel blockade, causing arterial dilation. Together they lower systemic vascular resistance and cardiac afterload, resulting in reduced blood pressure.

The dosage of Paniltri is individualized and set by the prescribing healthcare professional based on the patient’s clinical condition, response to therapy and any concomitant medications. Patients should follow the prescriber’s instructions and not adjust the dose without medical advice.

Paniltri is generally not recommended during pregnancy or lactation unless the potential benefit outweighs the risk. Ramipril belongs to the ACE‑inhibitor class, which is contraindicated in the second and third trimesters, and amlodipine and hydrochlorothiazide have limited safety data. Consultation with a healthcare provider is essential.

To order Paniltri, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, and will request verification of trade or institutional credentials. The sales team then provides pricing, availability, shipping details and any necessary import documentation.

Paniltri combines a thiazide diuretic, an ACE inhibitor and a calcium‑channel blocker in a single tablet, offering a convenient triple‑therapy option. Compared with separate monotherapies, it can improve adherence and provide synergistic blood‑pressure reduction, especially in patients requiring multi‑drug regimens. Alternative fixed‑dose combinations may contain different classes, such as ARBs instead of ACE inhibitors.

Paniltri tablets should be stored at ambient temperature, below 25 °C, in the original packaging. Keep the product away from moisture, direct sunlight and heat sources to maintain stability and potency throughout its shelf life.

Paniltri is taken orally, usually once daily, with or without food as directed by the prescriber. Swallow the tablet whole with a full glass of water. Do not crush, split or chew the tablet unless specifically advised by a healthcare professional.

Serious risks include angioedema, severe hypotension, acute renal impairment, electrolyte disturbances such as hyperkalemia, and hepatic dysfunction. Patients should be educated to seek immediate medical attention if they experience swelling of the face or throat, sudden dizziness, loss of urine output, or unexplained fatigue.

Paniltri is contraindicated in patients with known hypersensitivity to any of its components, severe renal impairment, significant hepatic disease, or a history of angioedema related to ACE‑inhibitor therapy. It should also be avoided in pregnant women beyond the first trimester and in individuals with uncontrolled hyperkalemia.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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