Product image of Olssa (Olmesartan Medoxomil, Amlodipine) supplied by GNH India

Olssa

Active Ingredient:
Olmesartan Medoxomil, Amlodipine
Origin:
EU

Olssa (Olmesartan Medoxomil, Amlodipine)

Olmesartan medoxomil, the active ingredient in Olssa, is a angiotensin II receptor blocker presented as a tablet for oral use. It treats hypertension and may be used in adults requiring blood pressure control.

GNH India supplies Olssa as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and pharmacies worldwide.

Manufacturer / TM Owner

Krka, D.D., Novo Mesto

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Indications & Clinical Uses

Olssa combines olmesartan medoxomil and amlodipine to address cardiovascular conditions that involve the renin‑angiotensin system and calcium‑channel mediated vascular tone.

  • Hypertension: helps lower systolic and diastolic blood pressure to reduce cardiovascular risk.
  • Hypertensive heart disease: assists in preventing left‑ventricular hypertrophy associated with long‑term high blood pressure.
  • Chronic kidney disease with hypertension: aids in slowing renal function decline by maintaining target blood pressure levels.

How It Works

  • Olmesartan medoxomil blocks the binding of angiotensin II to the AT1 receptor on vascular smooth‑muscle cells, preventing vasoconstriction and aldosterone release. Amlodipine inhibits calcium influx through L‑type channels in arterial smooth‑muscle, promoting vasodilation. The combined effect produces additive reduction of peripheral resistance and blood pressure.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate intensity.
  • Peripheral edema: swelling of ankles or feet.
  • Dizziness or light‑headedness, especially on standing.
  • Flushing: transient warmth or redness.
  • Fatigue: general feeling of tiredness.
  • Nausea: occasional upset stomach.

Serious or Rare Side Effects

  • Angio‑edema: rapid swelling of face, lips, tongue or throat.
  • Severe hypotension: symptomatic low blood pressure.
  • Hepatic dysfunction: elevated liver enzymes or jaundice.
  • Acute kidney injury: sudden reduction in renal function.
  • Heart block or severe bradycardia: markedly slow heart rate.
  • Allergic rash or Stevens‑Johnson syndrome: severe skin reactions.

Precautions & Warnings

Before initiating Olssa, clinicians should evaluate patient history and monitor relevant parameters.

  • Renal function: assess baseline creatinine and eGFR, adjust if impaired.
  • Hepatic function: check liver enzymes in patients with liver disease.
  • Electrolytes: monitor potassium and sodium levels, especially if combined with diuretics.
  • Pregnancy: avoid use; drug is contraindicated in the second and third trimesters.
  • Concomitant antihypertensives: watch for additive blood‑pressure lowering effects.
  • Store at ambient temperature: keep below 25°C, retain in original packaging and protect from moisture.

Avoid Interactions

Olssa may interact with several drug classes; awareness helps prevent adverse events.

Major Interactions (Avoid)

  • Aliskiren: concurrent use in diabetic patients can increase risk of renal impairment and hyperkalaemia.
  • Potassium‑sparing diuretics or supplements: may cause dangerous hyperkalaemia.
  • Strong CYP3A4 inhibitors (e.g., itraconazole, clarithromycin): can raise amlodipine levels.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may blunt antihypertensive response and affect renal function.
  • Lithium: increased lithium concentrations may occur.
  • Rifampicin: may reduce amlodipine exposure, lowering efficacy.

Frequently Asked Questions

Olssa is a fixed‑dose combination of olmesartan medoxomil and amlodipine that is prescribed to lower high blood pressure in adults. By controlling hypertension, it helps reduce the risk of cardiovascular events such as stroke or heart attack.

Olmesartan medoxomil is an angiotensin II receptor blocker; it prevents angiotensin II from binding to AT1 receptors on blood‑vessel walls, which stops vasoconstriction and lowers aldosterone‑driven fluid retention, leading to reduced blood‑pressure levels.

The dose of Olssa is individualized by the prescribing clinician based on the patient’s blood‑pressure readings, renal function and concomitant medications. The prescriber determines the appropriate strength and titration schedule.

Olssa is contraindicated in pregnancy, especially in the second and third trimesters, because angiotensin‑II blockade can harm the fetus. Limited data exist for breastfeeding; the precautionary approach is to avoid use unless the benefit clearly outweighs potential risk.

To request Olssa, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Olssa combines an ARB (olmesartan) with a calcium‑channel blocker (amlodipine), offering additive blood‑pressure reduction compared with using either component alone. It is often chosen over monotherapy when a single‑pill regimen is preferred for better adherence, and it provides an alternative to ACE‑inhibitor + CCB combinations.

Olssa tablets should be stored at ambient temperature, below 25 °C, in their original packaging to protect from moisture and light. Do not store in areas of high humidity or extreme heat.

Olssa 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 professional.

Serious adverse events include angio‑edema, severe hypotension, acute kidney injury, and rare hepatic dysfunction. Patients should seek immediate medical attention if they experience swelling of the face or throat, dizziness, fainting, or signs of liver injury.

Olssa should not be used by individuals with known hypersensitivity to olmesartan, amlodipine or any tablet excipients, pregnant women, or patients with severe hepatic impairment. Caution is also advised in those with significant renal dysfunction or uncontrolled heart failure.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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