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

Ivermectin Stada

Active Ingredient:
Ivermectin
Origin:
EU

Ivermectin Stada (Ivermectin)

Ivermectin, the active ingredient in Ivermectin Stada, is an anthelmintic presented as an oral tablet for oral use. It treats a range of parasitic worm and mite infections in adults and children as prescribed by a healthcare professional. The product conforms to European Union quality standards and is manufactured under strict Good Manufacturing Practice guidelines.

GNH India supplies Ivermectin Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with established distribution networks across Europe, Asia, Africa and the Americas.

Manufacturer / TM Owner

Stadapharm Gmbh

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Indications & Clinical Uses

Ivermectin is an anthelmintic that targets parasitic helminths and ectoparasites.

  • Onchocerciasis: reduces microfilarial load and helps prevent blindness in affected individuals.
  • Strongyloidiasis: eliminates intestinal Strongyloides stercoralis infection and prevents dissemination.
  • Scabies: eradicates Sarcoptes scabiei mites, relieving itching and skin lesions.
  • Lymphatic filariasis (combination therapy): contributes to parasite clearance when used with albendazole and diethylcarbamazine.
  • Other helminth infections: treats various nematode infections such as ascariasis and hookworm.

How It Works

  • Ivermectin binds selectively to glutamate‑gated chloride channels found in the nerve and muscle cells of parasites. This binding increases the permeability of the cell membrane to chloride ions, causing hyperpolarization, paralysis, and ultimately death of the parasite. Mammalian cells lack these channels, which accounts for the drug’s selective toxicity. The drug is absorbed systemically after oral administration and distributes widely, reaching effective concentrations in skin and soft tissues where parasites reside.

Side Effects

Ivermectin may cause adverse reactions, which are generally mild but can be serious in rare cases.

Common Side Effects

  • Nausea: mild stomach upset or queasiness.
  • Diarrhea: loose stools occurring shortly after dosing.
  • Dizziness: transient light‑headedness or vertigo.
  • Pruritus: itching at the site of parasite die‑off.

Serious or Rare Side Effects

  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Hepatotoxicity: elevated liver enzymes or hepatitis.
  • Neurological events: seizures, confusion, or ataxia.
  • Hypersensitivity: anaphylactic reactions requiring emergency care.

Precautions & Warnings

Before prescribing Ivermectin, clinicians should consider several precautionary measures to ensure safe use.

  • Pregnancy: use only if potential benefit justifies risk, as safety data are limited.
  • Breastfeeding: assess risk versus benefit; drug may be excreted in milk.
  • Concomitant CNS depressants: avoid or monitor for enhanced central nervous system effects.
  • Pre‑existing liver disease: adjust monitoring as ivermectin is metabolized hepatically.
  • Drug interactions: review patient’s medication list for known interactions.
  • Store at ambient temperature: keep below 25 °C in the original packaging, protect from moisture and light.

Avoid Interactions

Ivermectin can interact with other medicines, influencing its efficacy or safety.

Major Interactions (Avoid)

  • P‑glycoprotein inhibitors (e.g., clarithromycin, ketoconazole): may increase ivermectin plasma levels.
  • Strong inducers of CYP3A4 (e.g., rifampicin, carbamazepine): may reduce efficacy.

Moderate Interactions (Monitor Closely)

  • Anticoagulants (warfarin): monitor INR as ivermectin may potentiate anticoagulant effect.
  • CNS depressants (benzodiazepines, alcohol): observe for enhanced sedation.
  • Antiparasitic combination therapy (albendazole, diethylcarbamazine): adjust dosing per guidelines.

Frequently Asked Questions

Ivermectin Stada is prescribed to treat infections caused by parasitic worms and mites, including onchocerciasis (river blindness), strongyloidiasis, scabies, lymphatic filariasis when used in combination therapy, and a range of other helminth infections. It is administered under the direction of a qualified healthcare professional.

Ivermectin works by binding to glutamate‑gated chloride channels that are present in the nerve and muscle cells of parasites. This binding opens the channels, allowing an influx of chloride ions, which hyperpolarises the cells, leading to paralysis and death of the parasite while sparing human cells that lack these channels.

The dose of Ivermectin Stada is individualized by the prescribing clinician based on the specific indication, patient weight, age, severity of infection, and any relevant comorbidities. No fixed dosing regimen is provided here; the prescriber will calculate the appropriate amount for each patient.

Safety data for ivermectin in pregnancy are limited, so it should only be used when the potential benefit outweighs any possible risk to the fetus. During breastfeeding, the drug may be excreted in milk; clinicians should evaluate the risk‑benefit ratio before continuing treatment in nursing mothers.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity of Ivermectin Stada. GNH India supplies hospitals, pharmacies and procurement teams worldwide, and will request verification of trade or institutional credentials before providing pricing, availability, shipping details and any necessary import documentation.

Ivermectin is distinguished by its broad spectrum against both nematodes and ectoparasites, and its oral administration route. Compared with drugs such as albendazole or mebendazole, ivermectin often requires fewer doses but may have different interaction profiles. Choice of therapy depends on the parasite species, regional resistance patterns and patient‑specific factors.

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

Ivermectin Stada is supplied as an oral tablet that is taken by mouth with or without food, as directed by the prescriber. The tablet is swallowed whole with a glass of water; crushing or chewing is not recommended unless specifically instructed by a healthcare professional.

Serious adverse events, although rare, can include severe skin reactions such as Stevens‑Johnson syndrome, hepatotoxicity with elevated liver enzymes, neurological complications like seizures or ataxia, and life‑threatening hypersensitivity reactions. Patients should seek immediate medical attention if they experience any of these symptoms.

Ivermectin Stada is contraindicated in individuals with known hypersensitivity to ivermectin or any of the tablet excipients. Caution is also advised for patients with severe liver impairment, those taking strong P‑glycoprotein or CYP3A4 inhibitors, and in situations where pregnancy or breastfeeding risks outweigh benefits.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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