GNH USA

Europe — EMA

Olmesartan Medoxomilo + Hidroclorotiazida Viatris (Olmesartan Medoxomil, Hydrochlorothiazide)

GNH USA supplies Olmesartan Medoxomilo + Hidroclorotiazida (Olmesartan), an angiotensin II receptor blocker for hypertension.

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What is Olmesartan Medoxomil, Hydrochlorothiazide?

Olmesartan medoxil, the active ingredient in Olmesartan Medoxomilo + Hidroclorotiazida Viatris, is an angiotensin II receptor blocker presented as a oral tablet for hypertension management in adults. It combines olmesartan medoxil with hydrochlorothiazide to lower blood pressure through dual mechanisms.

GNH USA supplies Olmesartan Medoxomilo + Hidroclorotiazida Viatris as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and pharmacies worldwide.

What is Olmesartan Medoxomil, Hydrochlorothiazide used for?

Olmesartan medoxil/hydrochlorothiazide is indicated for cardiovascular conditions that involve elevated blood pressure and fluid retention. - Hypertension: improves blood pressure control when monotherapy is insufficient. - Congestive heart failure: assists in reducing preload and afterload, supporting symptom management. - Diabetic nephropathy: helps protect renal function by controlling systemic hypertension. - Post‑myocardial infarction: contributes to secondary prevention by maintaining target blood pressure levels.

What are the side effects of Olmesartan Medoxomil, Hydrochlorothiazide?

Adverse reactions may range from mild to severe and should be monitored during therapy.

Common Side Effects: - Dizziness or light‑headedness - Headache - Fatigue - Increased urination - Electrolyte disturbances (e.g., low potassium) - Mild gastrointestinal discomfort

Serious or Rare Side Effects: - Severe hypotension - Acute kidney injury - Hyperkalemia - Angio‑edema - Liver function abnormalities - Blood cell disorders such as agranulocytosis

What precautions apply to Olmesartan Medoxomil, Hydrochlorothiazide?

Before initiating therapy, consider the following safety measures: - Renal function: assess baseline creatinine and eGFR. - Electrolyte balance: monitor potassium and sodium levels regularly. - Pregnancy: avoid use; drug is contraindicated in the second and third trimesters. - Concomitant NSAIDs: use with caution due to increased risk of renal impairment. - Gout: monitor uric acid as thiazides may precipitate attacks. - Store at below 25°C: keep in the original packaging, protect from moisture and light.

What does Olmesartan Medoxomil, Hydrochlorothiazide interact with?

Olmesartan medoxil/hydrochlorothiazide may interact with several drug classes. Review the following:

Major Interactions (Avoid): - Aliskiren: combined use can cause excessive potassium loss and renal dysfunction. - Potassium‑sparing diuretics or supplements: risk of hyper‑kalemia. - Lithium: increased lithium levels may lead to toxicity.

Moderate Interactions (Monitor Closely): - NSAIDs: may blunt antihypertensive effect and affect renal function. - ACE inhibitors or ARBs: additive potassium elevation. - Antidiabetic agents: may require dose adjustment due to enhanced glucose lowering.

Frequently asked questions

What is Olmesartan Medoxomilo + Hidroclorotiazida used for?+
Olmesartan Medoxomilo + Hidroclorotiazida is a fixed‑dose combination of olmesartan medoxil and hydrochlorothiazide indicated for the treatment of hypertension, often when blood pressure is not adequately controlled with a single agent. It may also be used in patients with associated conditions such as heart failure or diabetic kidney disease, as part of a broader cardiovascular risk‑reduction strategy.
How does olmesartan medoxil work in this product?+
Olmesartan medoxil is an angiotensin II receptor blocker that selectively inhibits AT‑1 receptors, preventing angiotensin‑II‑mediated vasoconstriction and aldosterone secretion. This leads to relaxation of blood vessels and reduced sodium‑water retention, helping to lower systemic blood pressure.
What is the usual dose of this medication?+
The appropriate dose is determined by the prescribing clinician based on the patient’s blood pressure, renal function, and overall clinical profile. Dosage adjustments are made according to therapeutic response and tolerability, following local prescribing guidelines.
Is this medication safe during pregnancy or breastfeeding?+
Olmesartan Medoxomilo + Hidroclorotiazida is contraindicated in pregnancy, particularly in the second and third trimesters, because it can cause fetal toxicity. Breastfeeding is not recommended unless the benefits outweigh potential risks, and this decision should be made by a healthcare professional.
How do I order Olmesartan Medoxomilo + Hidroclorotiazida from GNH USA?+
To place an order, 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 pricing, availability, shipping details and any necessary import documentation.
How does this combination compare with other antihypertensive options?+
Compared with monotherapy using either an ARB or a thiazide diuretic, the olmesartan‑hydrochlorothiazide combo offers additive blood‑pressure reduction, often achieving target levels with a single tablet. It may be preferred over separate pills for adherence, but clinicians consider individual patient factors when selecting alternatives such as ACE‑inhibitor‑diuretic combos or calcium‑channel blocker‑based regimens.
What are the recommended storage conditions for this product?+
Store the tablets at temperatures below 25 °C in their original container, protecting them from moisture, heat and direct sunlight. Do not refrigerate or freeze the product.
How is Olmesartan Medoxomilo + Hidroclorotiazida administered?+
The medication is taken orally, usually once daily, with or without food. Patients should follow the prescribing clinician’s instructions regarding timing and whether the tablet should be swallowed whole or can be divided, if permitted.
What are the most serious risks associated with this medication?+
Serious adverse events include severe hypotension, acute kidney injury, hyper‑kalemia, angio‑edema and liver function abnormalities. Patients should seek immediate medical attention if they experience symptoms such as sudden dizziness, swelling of the face or throat, or marked changes in urine output.
Who should not take this medication?+
The product should be avoided in patients with known hypersensitivity to olmesartan, hydrochlorothiazide or any excipients, in pregnant women, and in individuals with severe renal impairment or electrolyte disturbances that could be worsened by a thiazide diuretic.
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
Viatris Limited
Origin
EU

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