Product image of Ivermectin Orifarm (Ivermectin) supplied by GNH India

Ivermectin Orifarm

Active Ingredient:
Ivermectin
Origin:
EU

Ivermectin Orifarm (Ivermectin)

Ivermectin, the active ingredient in Ivermectin Orifarm, is an anthelmintic presented as an oral tablet for oral use. It is employed to treat parasitic worm infections and certain ectoparasitic conditions in adult patients, acting on parasite nerve and muscle cells to cause paralysis and death of the organism.

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

Manufacturer / TM Owner

Orifarm Healthcare A/S

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Indications & Clinical Uses

Ivermectin is an antiparasitic agent used for several well‑established infections.

  • Onchocerciasis (river blindness): reduces microfilarial load and helps prevent disease progression.
  • Strongyloidiasis: eliminates intestinal nematode infection caused by Strongyloides stercoralis.
  • Scabies: treats both ordinary and crusted scabies caused by Sarcoptes scabiei.
  • Pediculosis (lice infestation): eradicates head and body lice infestations.

How It Works

  • Ivermectin binds selectively to glutamate‑gated chloride channels found in the nerve and muscle cells of susceptible parasites. This binding increases the influx of chloride ions, hyperpolarizing the cell membrane, leading to paralysis, loss of motility, and ultimately death of the parasite without affecting mammalian cells.

Side Effects

Ivermectin is generally well tolerated, but adverse reactions can occur.

Common Side Effects

  • Dizziness: transient feeling of light‑headedness.
  • Nausea: mild to moderate upset stomach.
  • Diarrhea: loose stools during treatment.
  • Abdominal pain: cramping or discomfort.
  • Pruritus: mild itching of the skin.
  • Headache: occasional tension‑type headache.

Serious or Rare Side Effects

  • Severe skin reactions: such as Stevens‑Johnson syndrome.
  • Hepatotoxicity: elevated liver enzymes or hepatitis.
  • Neurologic toxicity: seizures, ataxia, or altered mental status.
  • Hypotension: marked drop in blood pressure.
  • Anaphylaxis: acute allergic reaction requiring emergency care.
  • Visual disturbances: blurred vision or optic neuritis.

Precautions & Warnings

Before prescribing Ivermectin, clinicians should consider several safety measures.

  • Assess hypersensitivity: avoid in patients with known allergy to ivermectin or excipients.
  • Review hepatic function: use caution in severe liver disease and adjust therapy if needed.
  • Evaluate concomitant neurotoxic drugs: monitor for additive central nervous system effects.
  • Pregnancy considerations: avoid unless the potential benefit justifies the risk to the fetus.
  • Breastfeeding: weigh benefits against possible drug exposure to the infant.
  • Store at ambient temperature below 25°C: keep in the original pack, protect from moisture and direct sunlight.

Avoid Interactions

Ivermectin may interact with other medicines, requiring attention to the level of risk.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may increase ivermectin plasma concentrations.
  • P‑glycoprotein inhibitors (e.g., verapamil, quinidine): can raise systemic exposure.
  • Co‑administration with other neurotoxic agents (e.g., albendazole, levamisole): may enhance neurotoxicity.

Moderate Interactions (Monitor Closely)

  • Warfarin: potential increase in anticoagulant effect; monitor INR.
  • Macrolide antibiotics (e.g., erythromycin, clarithromycin): may modestly elevate ivermectin levels.
  • Antihistamines: may mask mild itching; observe for skin reactions.

Frequently Asked Questions

Ivermectin Orifarm is prescribed for parasitic infections such as onchocerciasis (river blindness), strongyloidiasis, scabies, and lice infestations. It works by targeting the parasites’ nervous system, leading to their paralysis and death, thereby clearing the infection in the treated individual.

Ivermectin binds to glutamate‑gated chloride channels that are present in many invertebrate parasites. This binding opens the channels, allowing an influx of chloride ions, which hyperpolarizes the cell membrane, causing paralysis of the parasite’s muscles and nerves and ultimately resulting in parasite death.

The dosage of Ivermectin Orifarm is determined by the prescribing clinician based on the specific indication, patient weight, age, and clinical condition. Only a qualified health professional should set the dose and treatment schedule for each individual patient.

Safety data for ivermectin in pregnancy and lactation are limited. It should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision must be made by a qualified health professional.

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 any necessary import documentation.

Ivermectin offers a broad spectrum of activity against many nematodes and ectoparasites, often with a single‑dose regimen, whereas some alternatives may require multiple doses or have a narrower spectrum. Its safety profile is well established, but choice of therapy should consider the specific parasite, resistance patterns and patient factors.

Ivermectin Orifarm should be stored at ambient temperature below 25 °C. Keep the tablets in their original packaging, protect them from moisture, excessive heat and direct sunlight to maintain product stability throughout its shelf life.

Ivermectin Orifarm is taken orally, usually as a tablet swallowed with water. The exact administration instructions, including whether it should be taken with food, are provided by the prescribing clinician based on the indication and patient needs.

Serious but rare risks include severe skin reactions such as Stevens‑Johnson syndrome, hepatotoxicity, neurologic toxicity (e.g., seizures, ataxia), hypotension and anaphylaxis. Patients should seek immediate medical attention if they experience any signs of these severe adverse events.

Ivermectin Orifarm should be avoided in individuals with known hypersensitivity to ivermectin or any of its excipients, in patients with severe liver impairment without medical supervision, and in pregnant women unless the therapeutic benefit justifies the potential risk. A healthcare professional should evaluate each case.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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