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

Ivermectine Sigillata

Active Ingredient:
Ivermectin
Origin:
EU

Ivermectine Sigillata (Ivermectin)

Ivermectin, the active ingredient in Ivermectine Sigillata, is an antiparasitic drug presented as an oral formulation for systemic use. It is employed to treat several helminthic and ectoparasitic infections, including river blindness, strongyloidiasis, scabies, and lice infestations, in adult and pediatric patients.

GNH India supplies Ivermectine Sigillata as a licensed, GDP‑compliant international pharmaceutical supplier, providing the product to hospitals, pharmacies and clinics worldwide under strict quality standards.

Manufacturer / TM Owner

Sigillata Limited

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Indications & Clinical Uses

Ivermectin acts on a broad range of parasitic infections by targeting the nervous system of the organisms.

  • Onchocerciasis (river blindness): reduces microfilarial load and prevents disease progression.
  • Strongyloidiasis: eradicates intestinal larvae and prevents autoinfection.
  • Scabies: eliminates Sarcoptes mites and resolves skin lesions.
  • Pediculosis (lice infestation): kills head and body lice, stopping transmission.
  • Other helminth infections: provides parasitological cure for various nematode species.

How It Works

  • Ivermectin binds selectively to glutamate‑gated chloride channels that are present in invertebrate nerve and muscle cells. This binding increases the permeability of the cell membrane to chloride ions, causing hyperpolarization, paralysis, and ultimately death of the parasite while having minimal effect on mammalian cells.

Side Effects

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

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Diarrhea: loose stools occurring shortly after dosing.
  • Dizziness: transient light‑headedness.
  • Pruritus: itching at the site of parasite death.
  • Headache: mild tension‑type headache.
  • Fatigue: temporary feeling of tiredness.

Serious or Rare Side Effects

  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Neurological events: seizures, encephalopathy, or ataxia.
  • Hepatic dysfunction: elevated liver enzymes or hepatitis.
  • Visual disturbances: blurred vision or optic neuritis.
  • Cardiac arrhythmias: rare conduction abnormalities.
  • Anaphylaxis: acute allergic reaction requiring emergency care.

Precautions & Warnings

Before prescribing Ivermectin, clinicians should consider patient‑specific factors and safety measures.

  • Pregnancy: safety data are limited; use only if potential benefit outweighs risk.
  • Breastfeeding: assess risk versus benefit; drug may be excreted in milk.
  • Liver impairment: dose adjustment may be needed in moderate to severe hepatic dysfunction.
  • Concomitant CNS depressants: monitor for additive central nervous system effects.
  • Storage: Store below 25°C: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Ivermectin may interact with other medicines, requiring careful management.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase ivermectin plasma concentrations.
  • P‑glycoprotein inhibitors (e.g., verapamil): can raise systemic exposure.

Moderate Interactions (Monitor Closely):\n- Anticoagulants (e.g., warfarin): monitor INR for potential enhancement of anticoagulant effect.

  • CNS depressants (e.g., benzodiazepines): observe for increased sedation.
  • Antiepileptic drugs (e.g., carbamazepine): may reduce ivermectin efficacy.
  • Immunosuppressants (e.g., cyclosporine): watch for altered drug levels.
  • Herbal supplements (e.g., St. John’s wort): possible induction of metabolism.

Frequently Asked Questions

Ivermectine Sigillata contains ivermectin, an antiparasitic indicated for onchocerciasis (river blindness), strongyloidiasis, scabies, pediculosis (lice infestation) and other helminth infections. It is prescribed by a qualified healthcare professional to eliminate the causative parasites and alleviate associated symptoms.

Ivermectin binds to glutamate‑gated chloride channels in the nervous system of parasites, increasing chloride ion influx. This hyperpolarizes the parasite’s cells, leading to paralysis and death, while sparing human cells because these specific channels are absent in mammals.

The dosage of Ivermectine Sigillata is determined by the prescribing clinician based on the specific infection, patient weight, age, and clinical condition. Only a qualified healthcare provider can set the appropriate regimen for each individual case.

Safety data for ivermectin in pregnancy are limited, and the drug should be used only if the potential benefit justifies the potential risk to the fetus. During breastfeeding, the decision should be based on a risk‑benefit assessment, as ivermectin can be excreted in breast milk.

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 both nematodes and ectoparasites, often requiring a single oral dose, whereas many alternative agents may need multiple doses or have a narrower spectrum. Its safety profile is well established, but choice of therapy should be guided by the specific parasite, resistance patterns and patient factors.

Ivermectine Sigillata should be stored at temperatures below 25 °C in its original packaging, protected from moisture and direct sunlight. Maintaining these conditions helps preserve the product’s potency and stability throughout its shelf life.

The product is taken orally, usually as a single dose or as directed by the prescriber. It should be swallowed with water on an empty stomach unless the prescribing information advises otherwise. Patients should follow the exact instructions provided by their healthcare professional.

Serious adverse events, though rare, can include severe skin reactions such as Stevens‑Johnson syndrome, neurological complications like seizures or encephalopathy, hepatic injury, visual disturbances, cardiac arrhythmias and anaphylaxis. Immediate medical attention is required if any of these occur.

Ivermectine Sigillata is contraindicated in individuals with known hypersensitivity to ivermectin or any excipients in the formulation. Caution is advised for patients with severe liver disease, pregnant women (unless benefits outweigh risks), and those taking medications that strongly inhibit CYP3A4 or P‑glycoprotein without appropriate monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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