GNH USA

Europe — EMA

Olartan-Plus (Olmesartan Medoxomil, Hydrochlorothiazide)

GNH USA supplies Olartan-Plus (Olmesartan medoxomil/Hydrochlorothiazide), an ARB/thiazide diuretic for hypertension. Request a quote for global supply.

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What is Olmesartan Medoxomil, Hydrochlorothiazide?

Olmesartan medoxomil and hydrochlorothiazide, the active ingredient in Olartan-Plus, is an Angiotensin II receptor blocker (ARB) combined with a thiazide diuretic presented as an oral tablet for oral use. It is used to lower high blood pressure in adult patients.

GNH USA supplies Olartan-Plus as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable sourcing for regulated markets.

What is Olmesartan Medoxomil, Hydrochlorothiazide used for?

Olartan-Plus, which combines an ARB and a thiazide diuretic, is indicated for the management of hypertension.

- Hypertension (essential): reduces systolic and diastolic blood pressure, aiding achievement of guideline‑recommended targets. - Hypertension requiring combination therapy: provides dual blockade of the renin‑angiotensin system and diuresis when a single agent does not achieve control. - Hypertension with fluid retention: adds a thiazide diuretic effect to lower plasma volume, enhancing overall blood pressure reduction. - Hypertension in patients with metabolic syndrome: improves blood pressure while modestly affecting electrolyte balance.

What are the side effects of Olmesartan Medoxomil, Hydrochlorothiazide?

Olartan-Plus may be associated with a range of adverse reactions, varying in frequency and severity.

Common Side Effects: - Dizziness - Headache - Fatigue - Increased urination

Serious or Rare Side Effects: - Severe hypotension - Acute kidney injury - Hyperkalemia - Allergic reactions (rash, angioedema)

What precautions apply to Olmesartan Medoxomil, Hydrochlorothiazide?

When prescribing Olartan-Plus, clinicians should consider several precautionary measures to ensure safe use. - Renal impairment: monitor kidney function and adjust therapy as needed. - Electrolyte imbalance: check serum potassium and sodium levels regularly. - Concomitant diuretics: assess risk of excessive diuresis and hypotension. - Pregnancy: avoid use unless benefits outweigh potential risks. - Elderly patients: start at lower dose and monitor for orthostatic symptoms. - Store at ambient temperature: keep below 25 °C in the original packaging, protected from moisture.

What does Olmesartan Medoxomil, Hydrochlorothiazide interact with?

Olartan-Plus can interact with other medicines, affecting its antihypertensive efficacy or safety profile.

Major Interactions (Avoid): - Potassium-sparing diuretics or supplements: may cause hyperkalemia. - NSAIDs (e.g., ibuprofen): can reduce antihypertensive effect and impair renal function. - Lithium: increased risk of lithium toxicity.

Moderate Interactions (Monitor Closely): - ACE inhibitors or other ARBs: additive blood pressure lowering, risk of hypotension. - Antihypertensive agents (beta‑blockers, calcium channel blockers): may require dose adjustments. - Antidiabetic drugs: monitor blood glucose as diuretics can affect glucose control.

Frequently asked questions

What is Olartan-Plus used for?+
Olartan-Plus is a fixed‑dose combination of olmesartan medoxomil and hydrochlorothiazide indicated for the treatment of hypertension. The ARB component blocks the angiotensin II receptor to relax blood vessels, while the thiazide diuretic promotes sodium and water excretion, together helping to lower elevated blood pressure in adult patients.
How does olmesartan medoxomil work?+
Olmesartan medoxomil selectively antagonizes the angiotensin II type 1 (AT₁) receptor, preventing angiotensin II‑induced vasoconstriction and aldosterone secretion. By inhibiting this pathway, it reduces peripheral vascular resistance and fluid retention, contributing to a sustained decrease in systolic and diastolic blood pressure.
What is the usual dose of Olartan-Plus?+
The dosage of Olartan-Plus is individualized by the prescribing physician based on the patient’s blood pressure, renal function, and response to therapy. The prescriber determines the appropriate strength and frequency, and any adjustments are made during follow‑up visits to achieve target blood pressure while minimizing adverse effects.
Is Olartan-Plus safe during pregnancy or breastfeeding?+
The safety of Olartan-Plus in pregnancy has not been established, and it is generally avoided because ARBs may cause fetal toxicity. Likewise, limited data exist for use while breastfeeding; therefore, the medication should only be used if the potential benefit outweighs the possible risk to the infant, under medical supervision.
How do I order Olartan-Plus from GNH USA?+
To request Olartan-Plus, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides a quotation, availability, shipping details—including any special handling—and the necessary import documentation.
How does Olartan-Plus compare with other antihypertensive options?+
Compared with monotherapy using either an ARB or a thiazide diuretic alone, Olartan-Plus offers combined blood‑pressure reduction in a single tablet, which can improve adherence and provide greater efficacy in patients whose pressure is not controlled by a single agent. It is generally considered when guideline‑recommended step‑up therapy is needed, while maintaining a safety profile similar to its individual components.
What are the storage requirements for Olartan-Plus?+
Olartan-Plus tablets should be stored at ambient temperature, preferably below 25 °C (77 °F). Keep the medication in its original blister pack or container, protect it from moisture and direct sunlight, and ensure it is out of reach of children. Do not store in a refrigerator or freezer unless otherwise directed by the supplier.
How is Olartan-Plus administered?+
Olartan-Plus is taken orally, usually once daily, with or without food, as directed by the prescribing clinician. The tablet should be swallowed whole with a glass of water and not chewed or split unless the prescriber specifically advises. Consistent timing each day helps maintain stable blood‑pressure control.
What are the most serious risks associated with Olartan-Plus?+
The most serious adverse events linked to Olartan-Plus include severe hypotension, acute kidney injury, hyperkalemia, and allergic reactions such as angioedema or rash. Patients should be monitored for signs of excessive blood‑pressure lowering, renal dysfunction, electrolyte disturbances, and hypersensitivity, and should seek immediate medical attention if any of these symptoms occur.
Who should not use Olartan-Plus?+
Olartan-Plus is contraindicated in individuals with known hypersensitivity to olmesartan, hydrochlorothiazide, or any component of the formulation. It should also be avoided in patients with severe renal impairment, hyperkalemia, or those taking other potassium‑sparing agents. Pregnant women and nursing mothers should not use it unless the potential benefit justifies the risk, and it is generally not recommended for children.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Olmesartan Medoxomil, Hydrochlorothiazide
Route
Oral Use
Manufacturer
Menarini International Operations Luxembourg S.A.
Origin
EU

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