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 dosage form for oral use. It is employed to treat parasitic infections caused by nematodes and other helminths in humans, adhering to EU quality standards and manufactured under GMP conditions.

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 anthelmintic that targets a range of helminthic diseases.

  • Onchocerciasis (river blindness): reduces microfilarial load and prevents disease progression.
  • Strongyloidiasis: eradicates intestinal larvae and prevents hyperinfection.
  • Scabies: eliminates Sarcoptes scabiei mites, relieving skin lesions.
  • Pediculosis (lice infestation): kills head lice and nits, controlling spread.

How It Works

  • Ivermectin binds selectively to glutamate‑gated chloride channels in the membranes of parasites. This binding increases chloride ion influx, causing hyperpolarization of the neuronal and muscular cells, leading to paralysis and death of the parasite without significant effect on mammalian cells.

Side Effects

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

Common Side Effects

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

Serious or Rare Side Effects

  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Hepatotoxicity: elevated liver enzymes or jaundice.
  • Neurologic toxicity: seizures, ataxia, or altered mental status.
  • Anaphylaxis: acute allergic reaction with airway compromise.
  • Vision changes: blurred vision or optic neuritis.
  • Severe hypotension: sudden drop in blood pressure.

Precautions & Warnings

When prescribing Ivermectin, clinicians should consider several safety measures.

  • Assess liver function: monitor hepatic enzymes before and during therapy.
  • Avoid in patients with known hypersensitivity: discontinue if allergic reaction occurs.
  • Use with caution in CNS disorders: patients with epilepsy may be at higher risk of neurotoxicity.
  • Review concomitant medications: potential interactions may alter drug levels.
  • Pregnancy: limited data, weigh benefits against potential risks.
  • Store at ambient temperature: keep in original packaging, protect from moisture and light.

Avoid Interactions

Ivermectin may interact with other medicines, requiring careful management.

Major Interactions (Avoid)

  • P‑glycoprotein inhibitors (e.g., clarithromycin): increase ivermectin plasma concentrations.
  • CNS depressants (e.g., benzodiazepines): enhance neurotoxic potential.
  • Warfarin: possible increase in anticoagulant effect.

Moderate Interactions (Monitor Closely)

  • Antifungals (e.g., ketoconazole): modestly raise ivermectin levels.
  • Antiepileptics (e.g., carbamazepine): may reduce ivermectin exposure.
  • St. John’s Wort: induces metabolism, potentially lowering efficacy.

Frequently Asked Questions

Ivermectin Orifarm is an oral anthelmintic indicated for the treatment of parasitic infections such as onchocerciasis (river blindness), strongyloidiasis, scabies, and pediculosis (lice infestation). It works by targeting the parasites responsible for these conditions, helping to eliminate them from the body.

Ivermectin binds to glutamate‑gated chloride channels found in the nerve and muscle cells of parasites. This binding opens the channels, allowing an influx of chloride ions, which hyperpolarizes the cells, leading to paralysis and death of the parasite while sparing human cells.

The specific dose of Ivermectin Orifarm is determined by the prescribing healthcare professional based on the type of infection, patient weight, age, and clinical guidelines. Patients should follow the exact dosage instructions provided by their prescriber.

Safety data for ivermectin use in pregnancy and lactation are limited. The drug should only be used if the potential benefit justifies any possible risk to the fetus or infant, and this decision must be made by a qualified healthcare provider.

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 is distinguished by its broad spectrum against many nematodes and ectoparasites, and its mechanism of targeting glutamate‑gated chloride channels. Compared with other antiparasitics such as albendazole or praziquantel, ivermectin often requires fewer doses and is effective for skin‑borne parasites like scabies and lice.

Ivermectin Orifarm should be stored at ambient temperature, preferably below 25 °C. Keep the product in its original packaging, protect it from moisture and direct sunlight, and ensure the container is tightly closed to maintain stability.

Ivermectin Orifarm is taken orally, usually as a tablet or capsule, with or without food as directed by the prescriber. The exact administration schedule depends on the indication and the dosage prescribed by the healthcare professional.

Serious risks, though rare, include severe skin reactions (such as Stevens‑Johnson syndrome), hepatotoxicity, neurologic toxicity (including seizures or altered mental status), and anaphylactic reactions. Patients should seek immediate medical attention if they experience any of these symptoms.

Ivermectin Orifarm should be avoided in individuals with known hypersensitivity to ivermectin or any of its excipients, in patients with certain central nervous system disorders without careful monitoring, and in pregnant women unless the potential benefit outweighs the risk as assessed by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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