Product image of Irbesartan/Hydrochloorthiazide 1a Pharma (Hydrochlorothiazide, Irbesartan) supplied by GNH India

Irbesartan/Hydrochloorthiazide 1a Pharma

Active Ingredient:
Hydrochlorothiazide, Irbesartan
Origin:
EU

Irbesartan/Hydrochloorthiazide 1a Pharma (Hydrochlorothiazide, Irbesartan)

Irbesartan, the active ingredient in Irbesartan/Hydrochloorthiazide 1a Pharma, is an angiotensin II receptor blocker presented as a combination tablet for oral use. It treats hypertension, often in conjunction with a thiazide diuretic, and is prescribed for adults needing blood pressure control.

GNH India supplies Irbesartan/Hydrochloorthiazide 1a Pharma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring consistent quality and regulatory compliance.

Manufacturer / TM Owner

1 A Pharma Gmbh

1
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Indications & Clinical Uses

Irbesartan/Hydrochlorothiazide acts on the renin‑angiotensin‑aldosterone system and renal sodium handling to lower blood pressure.

  • Essential hypertension: reduces systolic and diastolic pressure and lowers cardiovascular risk.
  • Hypertension requiring diuretic therapy: provides combined antihypertensive and diuretic effects for better control.
  • Resistant hypertension: adds an additional mechanism when monotherapy is insufficient.

How It Works

  • Irbesartan 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 decrease peripheral vascular resistance and plasma volume, resulting in lowered arterial blood pressure.

Side Effects

Common Side Effects

  • Dizziness: feeling light‑headed, especially after the first doses.
  • Headache: mild to moderate intensity.
  • Fatigue: general tiredness or lack of energy.
  • Increased urination: due to the diuretic component.
  • Electrolyte imbalance: low potassium or sodium levels.
  • Mild gastrointestinal upset: nausea or abdominal discomfort.

Serious or Rare Side Effects

  • Severe dehydration: excessive fluid loss leading to low blood pressure.
  • Acute kidney injury: sudden decline in renal function.
  • Hyperkalemia: dangerously high potassium levels.
  • Anaphylaxis: severe allergic reaction with rash, swelling, or breathing difficulty.
  • Blood disorders: such as agranulocytosis or leukopenia.
  • Liver injury: elevated liver enzymes or hepatitis.

Precautions & Warnings

Before initiating therapy, consider the following precautions:

  • Monitor blood pressure: check regularly to assess efficacy.
  • Assess renal function: evaluate serum creatinine and eGFR before and during treatment.
  • Check electrolytes: especially potassium and sodium levels.
  • Avoid in severe hepatic impairment: use with caution or consider alternatives.
  • Consider pregnancy status: category unknown; avoid unless benefits outweigh risks.
  • Store at ambient temperature: keep below 25°C, protect from moisture and light in the original container.

Avoid Interactions

Irbesartan/Hydrochlorothiazide may interact with several medicines. Review patient medication lists carefully.

Major Interactions (Avoid)

  • Potassium‑sparing diuretics or supplements: risk of hyperkalemia.
  • ACE inhibitors or other ARBs: additive effect on potassium and renal function.
  • Lithium: increased lithium levels and toxicity.
  • NSAIDs: may reduce antihypertensive effect and impair renal function.
  • Cyclosporine: increased risk of renal dysfunction.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may enhance antihypertensive effect.
  • Other diuretics: additive diuretic effect.
  • Antidiabetic agents: may increase hypoglycemic effect.
  • Antihistamines: may increase dizziness.
  • Alcohol: may potentiate hypotension.

Frequently Asked Questions

Irbesartan/Hydrochloorthiazide is a prescription medication used to treat hypertension. It combines an angiotensin II receptor blocker with a thiazide diuretic to lower blood pressure by relaxing blood vessels and reducing fluid volume.

Irbesartan blocks the AT1 receptors for angiotensin II, preventing vasoconstriction and aldosterone release. This leads to relaxed blood vessels and reduced blood pressure. The hydrochlorothiazide component increases urine output, further decreasing plasma volume.

The specific dose is determined by the prescribing clinician based on the patient’s condition, response, and other medications. Dosage adjustments are individualized and should follow the healthcare professional’s recommendation.

Pregnancy safety is unknown; the drug should be avoided unless the potential benefit justifies the risk. Breastfeeding considerations are also unclear, so a healthcare provider should be consulted before use in these situations.

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 import documentation.

Compared with single‑agent therapies, the combination offers dual mechanisms—vascular relaxation from the ARB and fluid reduction from the thiazide—often achieving better blood‑pressure control with a single pill, which can improve adherence.

Store the tablets at ambient temperature, below 25 °C. Keep them in the original packaging, protect from moisture and light, and keep out of reach of children.

The medication is taken orally, usually once daily, with or without food, as directed by a healthcare professional. Swallow the tablet whole; do not crush or chew unless instructed otherwise.

Serious risks include severe dehydration, acute kidney injury, hyperkalemia, and rare allergic reactions such as anaphylaxis. Patients should report symptoms like extreme weakness, swelling, rash, or sudden changes in urine output to their clinician promptly.

Patients with known hypersensitivity to irbesartan, hydrochlorothiazide, or any component of the formulation should avoid it. It is also contraindicated in severe renal or hepatic impairment and in individuals with certain electrolyte disorders unless closely monitored.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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