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

Micardisplus

Active Ingredient:
Hydrochlorothiazide, Telmisartan
Origin:
EU

Micardisplus (Hydrochlorothiazide, Telmisartan)

Telmisartan/Hydrochlorothiazide, the active ingredient in Micardisplus, is an angiotensin II receptor blocker / thiazide diuretic presented as an oral tablet for oral use. It treats hypertension in adult patients who need blood pressure control.

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

Manufacturer / TM Owner

Boehringer Ingelheim International Gmbh

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Indications & Clinical Uses

Micardisplus is indicated for the management of hypertension, a condition characterized by elevated arterial pressure.

  • Essential hypertension: reduces systolic and diastolic blood pressure, helping to prevent stroke and heart attack.
  • Secondary hypertension due to renal disease: assists in controlling pressure when other causes are present.
  • Hypertension requiring combination therapy: provides both ARB and diuretic effects in a single tablet.

How It Works

  • Telmisartan selectively blocks AT1 receptors, preventing angiotensin II‑mediated vasoconstriction and aldosterone release, while hydrochlorothiazide inhibits NaCl reabsorption in the distal convoluted tubule, promoting diuresis and reducing plasma volume. The combined actions lower systemic vascular resistance and cardiac preload, resulting in sustained blood‑pressure reduction.

Side Effects

Common Side Effects

  • Dizziness: sensation of light‑headedness, especially after standing.
  • Headache: mild to moderate tension‑type pain.
  • Fatigue: general feeling of tiredness.
  • Increased urination: due to the diuretic component.
  • Electrolyte imbalance: particularly low potassium levels.

Serious or Rare Side Effects

  • Severe allergic reaction: rash, swelling, or difficulty breathing.
  • Acute kidney injury: sudden decline in renal function.
  • Significant hypotension: marked drop in blood pressure causing faintness.
  • Hyperkalemia: elevated potassium that can affect heart rhythm.
  • Pancreatitis: inflammation of the pancreas presenting with abdominal pain.

Precautions & Warnings

Before initiating therapy, clinicians should consider the following precautions:

  • Renal function: assess creatinine and eGFR, adjust if impaired.
  • Electrolytes: monitor serum potassium and sodium regularly.
  • Pregnancy: contraindicated (Category D) due to fetal risk.
  • Concomitant ACE inhibitor or ARB therapy: avoid combined use to reduce renal injury risk.
  • Severe hepatic impairment: use with caution or avoid.
  • Store at room temperature: keep in the original pack, protect from moisture and direct sunlight.

Avoid Interactions

Micardisplus may interact with several medicines; careful review is required.

Major Interactions (Avoid)

  • Aliskiren in diabetic patients: increased risk of renal dysfunction.
  • Potassium‑sparing diuretics or supplements: risk of hyperkalemia.
  • Lithium: may raise lithium concentrations, leading to toxicity.
  • NSAIDs: can blunt antihypertensive effect and affect renal function.
  • ACE inhibitors or other ARBs: combined use may cause renal impairment.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: additive blood‑pressure lowering, monitor for excessive hypotension.
  • Calcium channel blockers: may enhance hypotensive response.
  • Antidiabetic agents: blood‑glucose levels may fall, requiring dose adjustment.

Frequently Asked Questions

Micardisplus is prescribed to lower high blood pressure in adults. It combines an angiotensin II receptor blocker with a thiazide diuretic, offering dual mechanisms that help control hypertension and reduce the risk of cardiovascular complications such as stroke and heart attack.

Telmisartan blocks the AT1 receptors for angiotensin II, preventing the hormone from causing blood‑vessel narrowing and aldosterone release. This leads to vasodilation and reduced fluid retention, which together lower systemic blood pressure.

The appropriate dose of Micardisplus is determined by the prescribing clinician based on the patient’s blood‑pressure readings, kidney function, and overall health. Dosage may be adjusted over time to achieve target blood‑pressure goals.

Micardisplus is classified as pregnancy Category D, indicating evidence of fetal risk, and should not be used by pregnant women. Safety during breastfeeding has not been established, so it is generally avoided unless the benefits outweigh potential risks.

To request Micardisplus, 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.

Micardisplus offers a fixed‑dose combination of an ARB and a thiazide diuretic, which can simplify therapy compared with taking separate tablets. Compared with ACE inhibitors, it has a lower incidence of cough, while the diuretic component adds volume‑reducing effects not present in ARB‑only products.

Store Micardisplus at room temperature, below 25 °C, in the original blister or bottle. Keep the container tightly closed, protect it from moisture and direct sunlight, and keep it out of reach of children.

Micardisplus is taken orally, usually once daily, with or without food as directed by the prescriber. Swallow the tablet whole with a glass of water; do not crush or split the tablet unless specifically instructed.

Serious risks include severe allergic reactions, acute kidney injury, marked hypotension, hyperkalemia, and, rarely, pancreatitis. Patients should seek immediate medical attention if they experience swelling, difficulty breathing, sudden loss of kidney function, very low blood pressure, or severe abdominal pain.

Micardisplus should be avoided in patients with known hypersensitivity to telmisartan, hydrochlorothiazide, or any component of the formulation, in pregnant women, and in individuals with severe renal or hepatic impairment unless specifically advised by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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