Product image of Myrosor (Ezetimibe, Rosuvastatin) supplied by GNH India

Myrosor

Active Ingredient:
Ezetimibe, Rosuvastatin
Origin:
EU

Myrosor (Ezetimibe, Rosuvastatin)

Ezetimibe and rosuvastatin, the active ingredients in Myrosor, are a cholesterol absorption inhibitor and an HMG‑CoA reductase inhibitor presented as an oral combination for lipid‑lowering therapy. They are used to reduce elevated LDL‑cholesterol and total cholesterol in adults with primary hypercholesterolemia or mixed dyslipidemia.

GNH India supplies Myrosor as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies, clinics and other health‑care institutions worldwide. The company adheres to stringent quality standards and provides regulatory support for import and distribution globally.

Manufacturer / TM Owner

Viatris Healthcare Nv/Sa

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Indications & Clinical Uses

Myrosor acts on lipid metabolism disorders and is indicated for the following conditions:

  • Primary hypercholesterolemia: lowers LDL‑cholesterol and total cholesterol levels.
  • Mixed dyslipidemia: improves overall lipid profile by reducing triglycerides and LDL‑cholesterol while raising HDL‑cholesterol.
  • High cardiovascular risk patients: provides additional LDL‑cholesterol reduction when statin monotherapy is insufficient.

How It Works

  • Ezetimibe selectively inhibits the Niemann‑Pick C1‑like 1 (NPC1L1) transporter in the intestinal brush border, reducing absorption of dietary and biliary cholesterol. Rosuvastatin competitively inhibits HMG‑CoA reductase, the rate‑limiting enzyme in hepatic cholesterol synthesis, leading to up‑regulation of LDL receptors and increased clearance of LDL particles from circulation.

Side Effects

Common Side Effects

  • Headache: mild to moderate intensity.
  • Abdominal pain: discomfort in the stomach area.
  • Diarrhea: loose stools occurring intermittently.
  • Myalgia: muscle aches without weakness.
  • Elevated liver enzymes: increased ALT/AST levels.
  • Nausea: feeling of sickness.

Serious or Rare Side Effects

  • Rhabdomyolysis: severe muscle breakdown with potential kidney injury.
  • Severe liver injury: marked elevation of hepatic enzymes or jaundice.
  • Allergic reactions: rash, pruritus, or angioedema.
  • Myopathy: muscle weakness with elevated CK.
  • Pancreatitis: inflammation of the pancreas.
  • Acute renal failure: sudden loss of kidney function.

Precautions & Warnings

Before initiating therapy, consider the following precautions:

  • Liver function monitoring: assess baseline and periodic ALT/AST.
  • Renal function assessment: evaluate creatinine clearance, especially in elderly.
  • Muscle symptom evaluation: inquire about unexplained muscle pain or weakness.
  • Active liver disease: avoid use in patients with ongoing hepatic impairment.
  • Concomitant medication review: adjust doses of drugs that increase statin exposure.
  • Store at room temperature: keep in the original pack, protect from moisture.

Avoid Interactions

Myrosor may interact with several medications. Review the following interaction categories:

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., clarithromycin, itraconazole): increase rosuvastatin exposure.
  • Gemfibrozil: heightened risk of myopathy.
  • Cyclosporine: elevated statin plasma levels.
  • High‑dose niacin: increased risk of muscle toxicity.
  • Cholestyramine or colestipol: reduce ezetimibe absorption.

Moderate Interactions (Monitor Closely)

  • Other statins: cumulative statin effect.
  • Fibrates (e.g., fenofibrate): monitor for muscle symptoms.
  • Warfarin: potential alteration of INR.
  • Digoxin: possible increased serum levels.
  • Antidiabetic agents: monitor glucose control.

Frequently Asked Questions

Myrosor is a prescription oral medication that combines ezetimibe and rosuvastatin to lower elevated LDL‑cholesterol and total cholesterol in adults with primary hypercholesterolemia or mixed dyslipidemia, helping reduce cardiovascular risk.

Ezetimibe blocks the NPC1L1 transporter in the intestinal lining, which limits the absorption of dietary and biliary cholesterol, thereby decreasing the amount of cholesterol delivered to the liver for incorporation into blood lipids.

The specific dose of Myrosor is determined by the prescribing clinician based on the patient’s lipid profile, cardiovascular risk, and tolerability. Dosage adjustments are made according to clinical response and safety considerations.

Myrosor is generally not recommended for use during pregnancy or while breastfeeding unless the potential benefit justifies the potential risk. Patients should discuss any pregnancy plans or nursing status with their healthcare provider.

To order Myrosor, 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 necessary import documentation.

Myrosor combines a cholesterol absorption inhibitor (ezetimibe) with a potent statin (rosuvastatin), offering greater LDL‑cholesterol reduction than either agent alone. This dual mechanism can be more effective than monotherapy with a statin or ezetimibe alone, especially in patients needing additional lipid control.

Store Myrosor at room temperature, below 25 °C, in the original packaging to protect it from moisture and light. Keep the container tightly closed and out of reach of children.

Myrosor is taken orally, usually once daily, with or without food, as directed by the prescribing physician. Swallow the tablet whole with a glass of water; do not crush or chew unless instructed otherwise.

Serious risks include rhabdomyolysis, severe liver injury, and allergic reactions such as rash or angioedema. Patients should promptly report unexplained muscle pain, weakness, dark urine, jaundice, or signs of an allergic response to their healthcare provider.

Myrosor should be avoided in patients with active liver disease, unexplained persistent elevations of hepatic enzymes, known hypersensitivity to ezetimibe or rosuvastatin, or those taking contraindicated medications such as strong CYP3A4 inhibitors without appropriate monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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