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 infections caused by parasitic worms and ectoparasites, including river blindness, strongyloidiasis, lymphatic filariasis, scabies and head lice, and is prescribed for patients requiring parasite eradication.

GNH India supplies Ivermectin Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company ensures quality manufacturing according to EU standards and provides reliable global distribution.

Manufacturer / TM Owner

Stada Arzneimittel Ag

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Indications & Clinical Uses

  • Ivermectin is used to treat a range of parasitic infections by targeting helminths and ectoparasites.
  • Onchocerciasis: reduces microfilarial load and helps prevent disease progression.
  • Strongyloidiasis: eliminates intestinal larvae and prevents disseminated infection.
  • Lymphatic filariasis: decreases adult worm burden and reduces transmission risk.
  • Scabies: eradicates the Sarcoptes mite, relieving skin lesions.
  • Pediculosis: kills head lice, controlling infestation.

How It Works

  • Ivermectin binds selectively to glutamate‑gated chloride channels in invertebrate nerve and muscle cells. This binding increases chloride ion influx, causing hyperpolarization of the cell membrane, leading to paralysis and death of the parasite. The drug exhibits high affinity for parasite receptors while having low affinity for mammalian channels, providing a therapeutic window for safe use in humans.

Side Effects

Ivermectin may cause a variety of adverse reactions, ranging from mild to severe.

Common Side Effects

  • Nausea: mild gastrointestinal upset.
  • Diarrhea: loose stools, usually self‑limiting.
  • Dizziness: transient light‑headedness.
  • Pruritus: skin itching, often at the site of parasite death.

Serious or Rare Side Effects

  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Neurological events: seizures, encephalopathy, or altered consciousness.
  • Hepatotoxicity: elevated liver enzymes or hepatitis.

Precautions & Warnings

  • Before prescribing Ivermectin, clinicians should consider several safety measures.
  • Assess infection type: confirm parasitic diagnosis before use.
  • Review concomitant medications: avoid drugs that affect central nervous system function.
  • Monitor liver function: patients with hepatic impairment may need dose adjustment.
  • Pregnancy and lactation: use only if benefits outweigh potential risks.
  • Store at ambient temperature: keep in original container, protect from moisture and light.

Avoid Interactions

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

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors: ketoconazole, itraconazole – may increase ivermectin levels.
  • P‑glycoprotein inhibitors: verapamil – may raise systemic exposure.

Moderate Interactions (Monitor Closely)

  • Warfarin: may enhance anticoagulant effect.
  • Anticonvulsants: carbamazepine – may reduce ivermectin concentration.
  • Macrolide antibiotics: erythromycin – potential modest increase in exposure.

Frequently Asked Questions

Ivermectin Stada is prescribed for several parasitic infections, including onchocerciasis (river blindness), strongyloidiasis, lymphatic filariasis, scabies, and pediculosis (head lice). The drug works by eliminating the parasites responsible for these diseases, helping to control symptoms and prevent further spread.

Ivermectin binds to glutamate‑gated chloride channels that are present in many invertebrates. This binding opens the channels, allowing an influx of chloride ions, which hyperpolarizes the nerve or muscle cell, leading to paralysis and death of the parasite while sparing human cells.

The appropriate dose of Ivermectin Stada is determined by the prescribing clinician based on the specific infection, patient weight, age, and clinical condition. Dosage regimens are individualized and should follow the prescriber’s instructions and local treatment guidelines.

Safety data for Ivermectin Stada 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 should be made by a qualified healthcare professional.

To request Ivermectin Stada, 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 belongs to the macrocyclic lactone class and offers a broad spectrum against both nematodes and ectoparasites. Compared with older agents such as albendazole or permethrin, ivermectin often requires fewer doses and has a distinct mechanism, making it a preferred option for several indications, though choice depends on the specific parasite and patient factors.

Store Ivermectin Stada 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 Stada is taken orally, usually as a single dose or a short course, depending on the indication. The tablet should be swallowed with water and can be taken with or without food, unless the prescriber advises otherwise.

Serious adverse events, although rare, can include severe skin reactions such as Stevens‑Johnson syndrome, neurological complications like seizures or encephalopathy, and liver injury. Patients should be monitored for any unusual symptoms and seek immediate medical attention if severe reactions occur.

Ivermectin Stada is contraindicated in individuals with known hypersensitivity to ivermectin or any component of the formulation. Caution is also advised for patients with severe hepatic impairment, and it should not be used in pregnant or nursing women unless clearly indicated by a healthcare professional.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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