GNH USA

Europe — EMA

Olmesartan/Amlodipine Krka (Olmesartan Medoxomil, Amlodipine)

GNH USA supplies Olmesartan/Amlodipine Krka (Olmesartan), an ARB for hypertension and high‑risk blood‑pressure control. Request a quote for global supply.

Request sourcing

1
Pack/s

What is Olmesartan Medoxomil, Amlodipine?

Olmesartan medoxil, the active ingredient in Olmesartan/Amlodipine Krka, is an angiotensin II receptor blocker (ARB) presented as a fixed‑dose combination tablet for oral use. It treats hypertension, often in patients who require additional blood pressure control beyond what a single agent can provide.

GNH USA supplies Olmesartan/Amlodipine Krka as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

What is Olmesartan Medoxomil, Amlodipine used for?

Olmesartan/Amlodipine Krka is used in the management of cardiovascular conditions that involve elevated blood pressure. - Hypertension: provides combined blockade of the renin‑angiotensin system and calcium‑channel mediated vasoconstriction to achieve better blood‑pressure control. - High‑risk hypertension: helps patients who have not reached target blood pressure with monotherapy, reducing cardiovascular risk. - Hypertensive patients with concomitant edema: amlodipine’s vasodilatory effect counteracts fluid retention often seen with ARBs.

What are the side effects of Olmesartan Medoxomil, Amlodipine?

Adverse reactions may vary in frequency and severity.

Common Side Effects: - Peripheral edema: swelling of the ankles or feet. - Headache: mild to moderate intensity. - Dizziness or light‑headedness, especially after standing. - Flushing: transient warmth and redness. - Fatigue: general feeling of tiredness. - Palpitations: awareness of heartbeat.

Serious or Rare Side Effects: - Severe hypotension: markedly low blood pressure. - Angio‑edema: rapid swelling of lips, tongue or airway. - Hepatic dysfunction: elevated liver enzymes. - Renal impairment: worsening kidney function. - Myocardial infarction: rare but reported in susceptible patients. - Hyperkalemia: elevated potassium levels.

What precautions apply to Olmesartan Medoxomil, Amlodipine?

When prescribing Olmesartan/Amlodipine Krka, clinicians should consider several safety aspects. - Renal function: assess baseline creatinine and monitor periodically. - Hepatic function: evaluate liver enzymes before initiating therapy. - Electrolytes: check potassium levels, especially if combined with potassium‑sparing agents. - Pregnancy: avoid use; teratogenic risk is associated with ARBs. - Elderly patients: start at lower dose and monitor for orthostatic hypotension. - Store at below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

What does Olmesartan Medoxomil, Amlodipine interact with?

Olmesartan/Amlodipine Krka may interact with several other medicines, requiring clinical attention.

Major Interactions (Avoid): - Dual renin‑angiotensin system blockade (e.g., ACE inhibitors, other ARBs): risk of severe hypotension, hyperkalemia and renal failure. - Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): increase amlodipine plasma concentrations.

Moderate Interactions (Monitor Closely): - Diuretics: may enhance antihypertensive effect and cause electrolyte disturbances. - Non‑steroidal anti‑inflammatory drugs (NSAIDs): can reduce antihypertensive efficacy and affect renal function. - Lithium: concurrent use may raise lithium levels, risking toxicity. - Simvastatin: amlodipine can increase statin concentration, raising myopathy risk.

Frequently asked questions

What is Olmesartan/Amlodipine Krka used for?+
Olmesartan/Amlodipine Krka is a fixed‑dose combination of an angiotensin II receptor blocker and a calcium‑channel blocker. It is prescribed to lower high blood pressure in adults, especially when a single agent does not achieve target blood‑pressure levels or when additional vascular protection is desired.
How does olmesartan medoxil work in this product?+
Olmesartan medoxil blocks AT1 receptors for angiotensin II, preventing the hormone from causing vasoconstriction and aldosterone‑driven sodium retention. This results in relaxed blood vessels and reduced fluid volume, contributing to lower blood pressure.
What is the usual dose of Olmesartan/Amlodipine Krka?+
The specific dose of Olmesartan/Amlodipine Krka is determined by the prescribing clinician based on the patient’s blood‑pressure readings, comorbidities and response to therapy. Dosage adjustments are made according to clinical guidelines and individual tolerance.
Is Olmesartan/Amlodipine Krka safe during pregnancy or breastfeeding?+
Olmesartan, an ARB, is contraindicated in pregnancy because it can cause fetal toxicity. Amlodipine is also not recommended unless clearly needed. Breastfeeding mothers should consult a healthcare professional, as limited data exist on excretion in milk.
How do I order Olmesartan/Amlodipine Krka 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 using separate olmesartan and amlodipine tablets?+
The fixed‑dose combination offers the same pharmacological actions as taking the two agents separately but simplifies the regimen to a single tablet, which can improve adherence. It also ensures a consistent ratio of the two drugs, reducing the risk of dosing errors.
What are the recommended storage conditions for Olmesartan/Amlodipine Krka?+
Store the tablets at temperatures below 25 °C in their original container, protected from moisture and direct sunlight. Do not expose the product to excessive heat or humidity, which could affect tablet integrity.
How is Olmesartan/Amlodipine Krka administered?+
The medication is taken orally, usually once daily, with or without food. Patients should swallow the tablet whole with a glass of water and follow the dosing schedule prescribed by their healthcare provider.
What are the most serious risks associated with Olmesartan/Amlodipine Krka?+
Serious risks include severe hypotension, angio‑edema, renal impairment, hepatic dysfunction and hyper‑kalemia. Patients should be monitored for sudden drops in blood pressure, swelling of the face or throat, and changes in kidney or liver function tests.
Who should not use Olmesartan/Amlodipine Krka?+
Individuals with known hypersensitivity to olmesartan, amlodipine or any excipients, pregnant women, and patients with severe hepatic or renal impairment should avoid this medication. Clinicians should also exercise caution in patients with a history of angio‑edema.
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, Amlodipine
Route
Oral Use
Manufacturer
Krka, D.D., Novo Mesto
Origin
EU

Related products