Product image of Olmesartan Medoxomil And Amlodipine Clydesdale Pharma (Olmesartan Medoxomil, Amlodipine) supplied by GNH India

Olmesartan Medoxomil And Amlodipine Clydesdale Pharma

Active Ingredient:
Olmesartan Medoxomil, Amlodipine
Origin:
EU

Olmesartan Medoxomil And Amlodipine Clydesdale Pharma (Olmesartan Medoxomil, Amlodipine)

Olmesartan medoxomil, the active ingredient in Olmesartan Medoxomil And Amlodipine Clydesdale Pharma, is an angiotensin II receptor blocker 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 India supplies Olmesartan Medoxomil And Amlodipine Clydesdale Pharma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Clydesdale Pharma Limited

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Indications & Clinical Uses

Olmesartan medoxomil and amlodipine is indicated for the management of high blood pressure within the renin‑angiotensin‑aldosterone system and calcium‑channel pathways.

  • Hypertension: provides additive blood‑pressure reduction when monotherapy is insufficient.
  • Isolated systolic hypertension in the elderly: improves systolic control while maintaining tolerability.
  • Hypertensive patients with concomitant peripheral edema from calcium‑channel blockers: amlodipine’s vasodilatory effect is balanced by olmesartan’s arterial relaxation.

How It Works

  • Olmesartan medoxil selectively blocks the AT1 receptor, preventing angiotensin II‑mediated vasoconstriction and aldosterone release. Amlodipine inhibits calcium influx into vascular smooth‑muscle cells, producing arterial dilation. The combination yields complementary reductions in systemic vascular resistance and blood pressure.

Side Effects

Both ingredients are generally well tolerated, but adverse reactions can occur.

Common Side Effects

  • Headache: mild to moderate intensity.
  • Peripheral edema: swelling of ankles or feet.
  • Dizziness or light‑headedness: especially after the first dose.
  • Flushing: transient warmth sensation.
  • Fatigue: general tiredness.
  • Nausea: occasional upset stomach.

Serious or Rare Side Effects

  • Angio‑edema: rapid swelling of face, lips or throat.
  • Severe hypotension: marked drop in blood pressure causing faintness.
  • Hepatic dysfunction: abnormal liver enzymes.
  • Hyperkalemia: elevated potassium levels.
  • Renal impairment: worsening kidney function.
  • Myocardial infarction: rare but reported in susceptible patients.

Precautions & Warnings

Before initiating therapy, clinicians should assess patient history and monitor relevant parameters.

  • Renal function: evaluate creatinine clearance and adjust if necessary.
  • Hepatic function: check liver enzymes in patients with liver disease.
  • Electrolytes: monitor potassium levels, especially if combined with potassium‑sparing agents.
  • Pregnancy: avoid use; teratogenic risk is associated with angiotensin‑II blockade.
  • Elderly patients: start at lower dose and titrate cautiously.
  • Store at ambient temperature: keep below 25°C, retain in original packaging and protect from moisture.

Avoid Interactions

Olmesartan medoxomil and amlodipine may interact with several drug classes; clinicians should review concomitant medications.

Major Interactions (Avoid)

  • Dual renin‑angiotensin system blockade (e.g., ACE inhibitors, other ARBs): risk of severe hypotension and renal failure.
  • Potassium‑sparing diuretics or supplements: may cause hyper‑kalemia.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): can blunt antihypertensive effect and affect renal function.
  • CYP3A4 inhibitors (e.g., clarithromycin, itraconazole): increase amlodipine plasma levels.
  • CYP3A4 inducers (e.g., rifampicin, carbamazepine): reduce amlodipine exposure.
  • Lithium: may increase serum lithium concentrations.
  • Alcohol: additive hypotensive effect, monitor blood pressure.

Frequently Asked Questions

Olmesartan Medoxomil And Amlodipine is a fixed‑dose combination indicated for the treatment of hypertension. It combines an angiotensin‑II receptor blocker with a calcium‑channel blocker to provide complementary blood‑pressure lowering effects in patients who need more than one agent to achieve target levels.

Olmesartan medoxomil selectively blocks AT1 receptors, preventing angiotensin II from causing vasoconstriction and aldosterone release. This leads to relaxation of blood vessels and reduced fluid retention, helping lower systemic blood pressure.

The prescribed dose is individualized by the treating physician based on the patient’s blood‑pressure readings, age, renal function and concomitant therapies. The prescriber determines the appropriate strength and titration schedule.

Use during pregnancy is contraindicated because angiotensin‑II receptor blockers can cause fetal toxicity. Breastfeeding is not recommended unless the benefits outweigh potential risks, and the decision should be made by a healthcare professional.

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 required import documentation.

The fixed‑dose combo offers the same pharmacologic actions as taking olmesartan and amlodipine separately, but with simplified dosing, improved adherence and potentially lower pill burden. Clinical studies show comparable efficacy and safety to the individual agents given together.

Store the tablets at ambient temperature, below 25 °C, in the original blister pack or container. Protect from moisture and direct sunlight to maintain potency throughout the shelf‑life.

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 prescribing clinician’s instructions regarding timing.

Serious adverse events include angio‑edema, severe hypotension, significant renal impairment, hyper‑kalemia and rare cases of myocardial infarction. Patients should seek immediate medical attention if they experience swelling of the face or throat, fainting, or sudden worsening of kidney function.

The combination is contraindicated in patients with known hypersensitivity to olmesartan, amlodipine or any excipients, in pregnant women, and in individuals taking another ARB or ACE inhibitor concurrently. Caution is also advised for patients with severe hepatic or renal impairment.

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GNH India Pharmaceuticals Limited

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Last updated:

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