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 formulation for systemic use. It is employed to eliminate a range of parasitic worms and ectoparasites in patients requiring prescription therapy.
GNH India supplies Ivermectin Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Stada Arzneimittel Ag

1
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Indications & Clinical Uses

  • Ivermectin Stada acts on a variety of helminth and ectoparasite infections, providing parasitic clearance in affected individuals.
  • Strongyloidiasis: effective in eradicating Strongyloides stercoralis infection.
  • Onchocerciasis: reduces microfilarial load and prevents disease progression.
  • Scabies: eliminates the Sarcoptes scabiei mite causing intense itching.
  • Pediculosis (lice): clears head and body lice infestations.
  • Other helminth infections: treats a broad spectrum of intestinal nematode infections.

How It Works

  • Ivermectin binds selectively to glutamate‑gated chloride channels in the nerve and muscle cells of invertebrates. This binding increases chloride ion influx, hyperpolarising the cell membrane, leading to paralysis and eventual death of the parasite while sparing mammalian cells due to the absence of these channels in humans.

Side Effects

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

Common Side Effects

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

Serious or Rare Side Effects

  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Hepatotoxicity: elevated liver enzymes or jaundice.
  • Neurologic events: seizures, confusion, or ataxia.
  • Anaphylaxis: acute allergic response requiring emergency care.

Precautions & Warnings

Before prescribing Ivermectin Stada, clinicians should consider several safety factors.

  • Pregnancy: safety not established; use only if potential benefit outweighs risk.
  • Breastfeeding: unknown excretion in milk; weigh maternal benefit against infant risk.
  • Renal or hepatic impairment: dose adjustment may be required.
  • Concomitant antiparasitics: monitor for additive toxicity.
  • Strong CYP3A4 inhibitors: avoid or adjust dose to prevent increased exposure.
  • Store below 25°C: keep in the original container, protect from moisture and light.

Avoid Interactions

Ivermectin may interact with other medicines, necessitating careful review.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may raise ivermectin plasma levels.
  • P‑glycoprotein inhibitors (e.g., verapamil): increase systemic exposure.
  • Warfarin: potential enhancement of anticoagulant effect.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampicin): may reduce therapeutic efficacy.
  • Other antiparasitic agents: risk of additive neurotoxicity.
  • Anticonvulsants: possible alteration of seizure threshold.

Frequently Asked Questions

Ivermectin Stada is prescribed for several parasitic diseases, including strongyloidiasis, onchocerciasis, scabies, pediculosis (lice) and a broad range of other helminth infections. It targets both intestinal nematodes and ectoparasites, providing a single oral therapy to clear the infestation.

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

The exact dose of Ivermectin Stada is determined by the prescribing clinician based on the specific indication, patient weight, age, and any relevant comorbidities. Dosage regimens are individualized and should follow the latest clinical guidelines or the prescriber’s judgment.

Safety data for Ivermectin Stada in pregnancy and lactation are limited. It is generally advised to avoid use during pregnancy unless the potential benefit justifies the risk. For breastfeeding mothers, the decision should be made after weighing the infant’s exposure against the mother’s therapeutic need.

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 (including any cold‑chain requirements) and the 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 different routes of administration. Its safety profile is favorable, but drug‑specific interactions and resistance patterns should be considered when selecting therapy.

Ivermectin Stada should be stored below 25 °C in its original packaging. Protect the product from moisture, direct sunlight and excessive heat to maintain potency throughout its shelf life.

Ivermectin Stada is taken orally, usually with water. The tablet (or other oral form) is swallowed whole and should be taken on an empty stomach unless the prescriber advises otherwise. The exact timing and any food restrictions are determined by the treating physician.

Serious adverse events, though rare, include severe skin reactions such as Stevens‑Johnson syndrome, hepatotoxicity, neurologic complications like seizures or ataxia, and anaphylactic reactions. Patients should be monitored for any signs of these conditions and seek immediate medical attention if they occur.

Ivermectin Stada is contraindicated in individuals with known hypersensitivity to ivermectin or any excipients in the formulation. Caution is also advised for patients with severe hepatic impairment, those taking strong CYP3A4 inhibitors, and pregnant women unless the therapeutic benefit outweighs potential risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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