Product image of Mogilarta (Hydrochlorothiazide, Telmisartan) supplied by GNH India

Mogilarta

Active Ingredient:
Hydrochlorothiazide, Telmisartan
Origin:
EU

Mogilarta (Hydrochlorothiazide, Telmisartan)

Hydrochlorothiazide and Telmisartan, the active ingredients in Mogilarta, are a thiazide diuretic and an angiotensin II receptor blocker presented as an oral tablet for systemic use. They treat hypertension in adult patients.

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

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

Mogilarta combines an angiotensin II receptor blocker with a thiazide diuretic to manage elevated blood pressure across the hypertension spectrum.

  • Essential hypertension: lowers systolic and diastolic pressure to reduce cardiovascular risk.
  • Secondary hypertension: assists in blood‑pressure control when underlying causes are being treated.
  • Isolated systolic hypertension: improves pulse pressure in older adults.

How It Works

  • Telmisartan selectively blocks angiotensin II type 1 (AT1) receptors, preventing vasoconstriction and aldosterone release, while hydrochlorothiazide inhibits NaCl reabsorption in the distal convoluted tubule, increasing urinary sodium and water excretion. The combined actions reduce peripheral vascular resistance and plasma volume, resulting in sustained blood‑pressure reduction.

Side Effects

Mogilarta may cause a range of adverse reactions, most of which are mild and reversible.

Common Side Effects

  • Dizziness or light‑headedness
  • Headache
  • Fatigue or weakness
  • Increased urinary frequency
  • Electrolyte disturbances (e.g., low potassium)
  • Mild gastrointestinal upset

Serious or Rare Side Effects

  • Severe dehydration or electrolyte imbalance
  • Acute kidney injury or worsening renal function
  • Hyperkalemia, especially with potassium‑sparing agents
  • Angioedema or severe allergic reaction
  • Significant hypotension leading to syncope

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient‑specific factors and monitor for potential complications.

  • Renal function: assess baseline creatinine and eGFR, then monitor periodically.
  • Electrolytes: check serum potassium and sodium, especially when combined with other diuretics.
  • Elderly patients: start at lower dose and monitor for orthostatic hypotension.
  • Hepatic impairment: use with caution; dose adjustment may be required.
  • Concomitant NSAIDs: avoid or monitor renal function closely.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Mogilarta can alter the effects of several other medicines; awareness of interaction severity helps guide safe use.

Major Interactions (Avoid)

  • Aliskiren in diabetic patients: risk of renal dysfunction and hyperkalemia.
  • Potassium‑sparing diuretics or supplements: may cause dangerous hyperkalemia.
  • ACE inhibitors or other ARBs: additive effect on potassium and renal function.
  • Lithium: increased lithium levels and toxicity.
  • Cyclosporine: heightened risk of nephrotoxicity.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may blunt antihypertensive response and affect renal function.
  • CYP2C9 inhibitors (e.g., fluconazole): can raise telmisartan concentrations.
  • Antacids containing aluminum or magnesium: may reduce hydrochlorothiazide absorption.

Frequently Asked Questions

Mogilarta is prescribed to lower high blood pressure in adults. It combines telmisartan, an angiotensin II receptor blocker, with hydrochlorothiazide, a thiazide diuretic, to achieve better control of hypertension than either component alone.

Telmisartan blocks AT1 receptors, preventing angiotensin II‑mediated vasoconstriction and aldosterone release. Hydrochlorothiazide reduces sodium and water reabsorption in the distal tubule, decreasing plasma volume. Together they lower peripheral resistance and blood volume, producing a sustained antihypertensive effect.

The specific dose of Mogilarta is determined by the prescribing clinician based on the patient’s blood‑pressure level, renal function, and other individual factors. Dosage adjustments are made according to clinical response and tolerability.

The safety of Mogilarta in pregnancy and lactation has not been established. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and this decision must be made by a qualified healthcare professional.

To place an order, submit an enquiry on the Mogilarta 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.

Mogilarta offers the convenience of a single‑tablet regimen that combines an ARB with a thiazide diuretic, often providing more consistent blood‑pressure control than monotherapy. Compared with separate tablets, it may improve adherence, but clinicians must consider individual patient tolerance and potential drug‑interaction profiles.

Mogilarta tablets should be stored at room temperature, below 25 °C, in the original packaging. Keep them away from moisture, heat and direct sunlight to maintain product stability.

Mogilarta 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 or chew unless specifically instructed.

Serious risks include severe dehydration, electrolyte imbalance (especially low potassium), acute kidney injury, hyperkalemia, and rare cases of angioedema or severe hypotension. Patients should be monitored regularly for these conditions, particularly when starting therapy or adjusting doses.

Mogilarta is contraindicated in patients with known hypersensitivity to either component, severe renal impairment, anuria, or those taking aliskiren in combination with diabetes. Caution is also advised for individuals with hepatic disease, electrolyte disturbances, or who are pregnant.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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