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

Myrosor

Active Ingredient:
Ezetimibe, Rosuvastatin
Origin:
EU

Myrosor (Ezetimibe, Rosuvastatin)

Ezetimibe/rosuvastatin, the active ingredient in Myrosor, is a statin and cholesterol absorption inhibitor presented as a tablet for oral use. It lowers LDL‑C and total cholesterol in adults with hypercholesterolemia or mixed dyslipidemia.
GNH India supplies Myrosor as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Viatris Healthcare Nv/Sa

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Indications & Clinical Uses

Myrosor is used to manage lipid disorders by targeting cholesterol synthesis and absorption pathways.

  • Hypercholesterolemia: reduces elevated LDL‑C and total cholesterol levels.
  • Mixed dyslipidemia: improves the overall lipid profile by lowering LDL‑C and triglycerides while raising HDL‑C.
  • Primary prevention of cardiovascular events: helps lower risk in patients with high cholesterol who have additional risk factors.

How It Works

  • Ezetimibe blocks the Niemann‑Pick C1‑like 1 (NPC1L1) transporter in the intestinal brush border, reducing dietary and biliary cholesterol absorption. Rosuvastatin competitively inhibits HMG‑CoA reductase, the key enzyme in hepatic cholesterol synthesis. The combined effect decreases circulating LDL‑C and total cholesterol, while modestly increasing HDL‑C.

Side Effects

Adverse reactions may occur with Myrosor and should be monitored.

Common Side Effects

  • Headache: mild to moderate intensity.
  • Myalgia: muscle aches without weakness.
  • Gastrointestinal discomfort: nausea, abdominal pain, or diarrhea.
  • Elevated liver enzymes: transient increases in ALT/AST.
  • Fatigue: general tiredness.

Serious or Rare Side Effects

  • Rhabdomyolysis: severe muscle breakdown with dark urine.
  • Acute hepatitis: marked elevation of liver enzymes with jaundice.
  • Severe allergic reaction: rash, swelling, or anaphylaxis.
  • Renal impairment: worsening kidney function in susceptible patients.
  • Myopathy with statin‑related muscle toxicity.

Precautions & Warnings

Before prescribing Myrosor, clinicians should consider several safety aspects.

  • Liver function monitoring: assess baseline ALT/AST and repeat periodically.
  • Renal function assessment: evaluate creatinine clearance in patients with kidney disease.
  • Drug interactions: review concomitant medications that affect statin metabolism.
  • Pregnancy and lactation: avoid use due to unknown safety profile.
  • Patient education: advise reporting unexplained muscle pain or weakness.
  • Store at ambient temperature: keep below 25°C in the original container, protect from moisture and light.

Avoid Interactions

Myrosor may interact with other medicines, requiring careful management.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., clarithromycin, itraconazole): increase rosuvastatin exposure.
  • Cyclosporine: markedly raises rosuvastatin levels, raising risk of myopathy.
  • Gemfibrozil: enhances statin‑related muscle toxicity.

Moderate Interactions (Monitor Closely)

  • Antacids containing aluminum or magnesium: may reduce ezetimibe absorption.
  • Warfarin: potential alteration of INR, requiring monitoring.
  • Niacin: may increase risk of liver enzyme elevations.

Frequently Asked Questions

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

Ezetimibe blocks intestinal cholesterol absorption by inhibiting the NPC1L1 transporter, while rosuvastatin reduces hepatic cholesterol synthesis by inhibiting HMG‑CoA reductase. Together they lower circulating LDL‑C and total cholesterol levels.

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

The safety of Myrosor in pregnancy and lactation has not been established. It is generally avoided in pregnant or nursing women unless the potential benefit justifies the potential risk to the fetus or infant.

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 required import documentation.

Myrosor combines a statin (rosuvastatin) with a cholesterol absorption inhibitor (ezetimibe), offering a dual mechanism that can achieve greater LDL‑C reduction than a statin alone. It is often considered when monotherapy does not reach target lipid levels.

Myrosor tablets should be stored at ambient temperature, below 25 °C, in the original packaging to protect from moisture and light. Do not store in areas with high humidity or direct sunlight.

Myrosor is taken orally, usually once daily, with or without food, as directed by the prescribing healthcare professional. Swallow the tablet whole with a glass of water.

Serious risks include rhabdomyolysis (severe muscle breakdown), acute hepatitis, and severe allergic reactions such as anaphylaxis. Patients should promptly report unexplained muscle pain, weakness, dark urine, or signs of liver injury.

Myrosor is contraindicated in patients with active liver disease, unexplained persistent elevations of hepatic enzymes, known hypersensitivity to ezetimibe, rosuvastatin, or any excipients, and in individuals taking contraindicated medications such as strong CYP3A4 inhibitors or gemfibrozil.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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