Product image of Ivermectine Substipharm (Ivermectin) supplied by GNH India

Ivermectine Substipharm

Active Ingredient:
Ivermectin
Origin:
EU

Ivermectine Substipharm (Ivermectin)

Ivermectin, the active ingredient in Ivermectine Substipharm, is a Anthelmintic presented as an oral dosage form for oral administration. It targets a variety of parasitic worm and ectoparasite infections, providing therapeutic benefit in affected individuals across age groups. It is indicated for several neglected tropical diseases and is included in WHO‑endorsed treatment guidelines.

GNH India supplies Ivermectine Substipharm as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring consistent quality and regulatory compliance for global health programs, including public health initiatives and private sector procurement.

Manufacturer / TM Owner

Substipharm

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Indications & Clinical Uses

Ivermectin is an antiparasitic agent used to treat infections caused by helminths and ectoparasites.

  • Onchocerciasis: reduces microfilarial load and helps prevent ocular complications.
  • Strongyloidiasis: eliminates intestinal larvae and prevents hyperinfection.
  • Scabies: eradicates Sarcoptes mites, relieving skin lesions.
  • Lymphatic filariasis: decreases microfilariae, contributing to transmission control.
  • Other helminth infections: provides broad‑spectrum activity against various nematodes.

How It Works

  • Ivermectin binds selectively to glutamate‑gated chloride channels that are present in the nerve and muscle cells of invertebrates. This binding increases the permeability of the cell membrane to chloride ions, leading to hyperpolarization, paralysis and eventual death of the parasite. The drug’s high affinity for these channels results in sustained opening, and the resulting ionic imbalance disrupts neuromuscular transmission in the parasite.

Side Effects

Ivermectin may cause a range of adverse reactions, most of which are mild and reversible.

Common Side Effects

  • Dizziness: transient sensation of light‑headedness.
  • Nausea: mild to moderate stomach upset.
  • Diarrhea: loose stools occurring shortly after dosing.
  • Itching: localized pruritus at the site of parasite die‑off.

Serious or Rare Side Effects

  • Severe skin reactions: such as Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Neurologic events: including seizures, altered consciousness or visual disturbances.

Precautions & Warnings

When prescribing Ivermectine Substipharm, clinicians should observe several safety considerations.

  • Pregnancy: safety not established; avoid unless potential benefit outweighs risk.
  • Breastfeeding: unknown excretion in milk; consider risk versus benefit.
  • Renal impairment: use with caution and monitor plasma levels if severe.
  • Drug interactions: review concomitant medications for CYP3A4 modulators.
  • Store at ambient temperature: keep in original packaging, protect from moisture and light.

Avoid Interactions

Ivermectin can interact with other medicines that affect its metabolism or transport.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampicin, carbamazepine): may markedly reduce ivermectin exposure.
  • Warfarin: concurrent use may enhance anticoagulant effect and increase bleeding risk.

Moderate Interactions (Monitor Closely)

  • Macrolide antibiotics (e.g., erythromycin, clarithromycin): can increase ivermectin plasma concentrations.
  • Azole antifungals (e.g., ketoconazole, itraconazole): may raise drug levels.
  • P‑glycoprotein inhibitors (e.g., verapamil, amiodarone): may modestly increase exposure.

Frequently Asked Questions

Ivermectine Substipharm contains ivermectin, which is indicated for onchocerciasis, strongyloidiasis, scabies, lymphatic filariasis and a range of other helminth infections. These are parasitic diseases that affect skin, eyes, and internal organs, and the medication is used as part of WHO‑endorsed treatment protocols.

Ivermectin binds to glutamate‑gated chloride channels in the nerve and muscle cells of invertebrate parasites. This increases chloride ion flow, causing hyperpolarisation of the cell membrane, leading to paralysis and death of the parasite while sparing human cells that lack these channels.

The exact dose of Ivermectine Substipharm is set by the prescribing clinician based on the specific indication, patient weight, age, and any relevant comorbidities. Dosage regimens vary between diseases and are not standardized in this description.

Safety data for ivermectin in pregnancy and lactation are limited. The product is classified as pregnancy category unknown, and use is generally avoided unless the potential benefit justifies the potential risk. Breastfeeding mothers should discuss possible exposure with their 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 offers a broad‑spectrum oral option for several neglected tropical diseases, often requiring fewer doses than alternatives such as albendazole or diethylcarbamazine. Its selective mechanism provides a favorable safety profile, though choice of therapy depends on local resistance patterns, disease severity and patient factors.

Ivermectine Substipharm should be stored at ambient temperature, below 25 °C, in its original packaging. The container should be kept tightly closed, protected from moisture, light and excessive heat to maintain product stability.

The medication is taken orally, usually with a full glass of water. It may be administered with or without food, depending on the prescriber’s instructions. Patients should follow the exact dosing schedule provided by their healthcare professional.

Serious adverse events, although rare, include severe skin reactions such as Stevens‑Johnson syndrome, neurologic complications like seizures or altered consciousness, and visual disturbances. Any sudden or severe symptoms should prompt immediate medical evaluation.

Ivermectine Substipharm is contraindicated in patients with known hypersensitivity to ivermectin or any excipients in the formulation. Caution is advised for individuals with severe hepatic or renal impairment, and it should be avoided in pregnant women unless the benefit outweighs the risk.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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