Product image of Lipanthylnano (Fenofibrate) supplied by GNH India

Lipanthylnano

Active Ingredient:
Fenofibrate
Origin:
EU

Lipanthylnano (Fenofibrate)

Fenofibrate, the active ingredient in Lipanthylnano, is a fibrate presented as an oral dosage form for oral use. It is used to lower elevated triglyceride levels and modify lipid profiles in patients with dyslipidemia.
GNH India supplies Lipanthylnano 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

Fenofibrate acts on lipid metabolism pathways to improve abnormal blood lipid levels.

  • Hypertriglyceridemia: reduces very‑low‑density lipoprotein triglycerides and lowers plasma triglyceride concentrations.
  • Mixed dyslipidemia: decreases triglycerides while modestly raising high‑density lipoprotein cholesterol.
  • Primary hypercholesterolemia (adjunct therapy): used together with statins to further improve lipid control when statin therapy alone is insufficient.

How It Works

  • Fenofibrate activates peroxisome proliferator‑activated receptor alpha (PPARα), a nuclear transcription factor that up‑regulates genes involved in fatty‑acid β‑oxidation and down‑regulates enzymes responsible for triglyceride synthesis, leading to increased clearance of triglyceride‑rich lipoproteins and modest increases in HDL‑cholesterol.

Side Effects

Common Side Effects

  • Gastrointestinal discomfort: nausea, abdominal pain, or dyspepsia.
  • Headache: mild to moderate intensity.
  • Muscle pain: myalgia without significant enzyme elevation.
  • Elevated liver enzymes: transient increases in ALT or AST.

Serious or Rare Side Effects

  • Rhabdomyolysis: severe muscle breakdown with potential renal failure.
  • Severe liver injury: hepatitis or hepatic failure.
  • Acute pancreatitis: inflammation of the pancreas presenting with abdominal pain and elevated enzymes.
  • Anaphylactic reaction: rare but potentially life‑threatening hypersensitivity.
  • Myopathy with renal impairment: muscle toxicity accompanied by reduced kidney function.

Precautions & Warnings

Fenofibrate should be used with careful clinical monitoring.

  • Liver function monitoring: assess baseline and periodic hepatic enzymes.
  • Renal function assessment: evaluate creatinine clearance before initiation and during therapy.
  • Muscle disorder evaluation: inquire about myalgia or unexplained weakness.
  • Statin co‑therapy review: consider dose adjustments or alternative agents to reduce myopathy risk.
  • Contraindication in severe hepatic impairment: avoid use in patients with active liver disease.
  • Store at below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Fenofibrate may interact with several medicines, requiring attention to co‑administration.

Major Interactions (Avoid)

  • Gemfibrozil: markedly increases risk of myopathy and rhabdomyolysis.
  • Cyclosporine: elevates fenofibrate plasma concentrations, enhancing toxicity.
  • High‑dose statins (e.g., rosuvastatin ≥20 mg): synergistic risk of severe muscle injury.

Moderate Interactions (Monitor Closely)

  • Warfarin: may potentiate anticoagulant effect, requiring INR monitoring.
  • Oral hypoglycemics (e.g., sulfonylureas): can enhance hypoglycaemia; monitor glucose levels.
  • Bile‑acid sequestrants (e.g., cholestyramine): may reduce fenofibrate absorption; separate dosing times.

Frequently Asked Questions

Lipanthylnano, containing fenofibrate, is prescribed for patients with hypertriglyceridemia, mixed dyslipidemia, and as an adjunct to statin therapy in primary hypercholesterolemia when additional lipid control is needed.

Fenofibrate activates the nuclear receptor PPARα, which increases the oxidation of fatty acids and reduces the synthesis of triglycerides, leading to lower plasma triglyceride concentrations and modest increases in HDL‑cholesterol.

The specific dose of Lipanthylnano is determined by the prescribing clinician based on the patient’s lipid profile, renal and hepatic function, and any concomitant medications. Patients should follow the prescriber’s instructions.

Fenofibrate is classified as Pregnancy Category B, indicating no evidence of risk in animal studies but insufficient human data. It should be used in pregnancy only if clearly needed, and breastfeeding mothers should consult their physician before use.

To place an order, 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.

Compared with statins, fenofibrate primarily lowers triglycerides and modestly raises HDL‑cholesterol, while statins are more potent at reducing LDL‑cholesterol. Fenofibrate is often added to statin therapy when triglyceride levels remain high despite statin use.

Lipanthylnano should be stored at temperatures below 25 °C, in its original packaging, protected from moisture and direct sunlight to maintain product stability.

Lipanthylnano is taken orally, usually with a meal to improve absorption. Patients should swallow the tablet whole with water and follow the dosing schedule prescribed by their healthcare provider.

The most serious risks include rhabdomyolysis, severe liver injury, and acute pancreatitis. Patients should promptly report unexplained muscle pain, dark urine, jaundice, or severe abdominal pain to their physician.

Lipanthylnano is contraindicated in patients with severe hepatic impairment, active liver disease, or known hypersensitivity to fenofibrate or other fibrates. Caution is also advised for individuals with renal insufficiency or a history of muscle disorders.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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