Is ivermectin safe to use for treating parasitic infections?

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Last updated: September 16, 2025View editorial policy

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Ivermectin Safety for Parasitic Infections

Ivermectin is safe and effective for treating specific parasitic infections when used at appropriate FDA-approved doses, with a well-established safety profile spanning over 25 years of clinical use. 1, 2

Approved Indications

Ivermectin is FDA-approved for:

  • Intestinal strongyloidiasis (200 mcg/kg as a single oral dose)
  • Onchocerciasis (150 mcg/kg as a single oral dose)
  • Off-label uses with strong evidence:
    • Crusted (Norwegian) scabies
    • Pediculosis pubis (pubic lice)
    • Scabies (200 mcg/kg orally, repeated in 2 weeks) 3

Safety Profile

  • Mechanism of action: Binds selectively to glutamate-gated chloride ion channels in invertebrate nerve and muscle cells, causing paralysis and death of parasites 1
  • Metabolism: Primarily by CYP3A4 in the liver with a plasma half-life of approximately 18 hours 1
  • Excretion: Almost exclusively in feces over approximately 12 days, with less than 1% excreted in urine 1

Common Adverse Effects

  • Mild to moderate reactions are common but typically transient:

    • Edema
    • Rash
    • Headache
    • Ocular complaints 1, 2
  • Mazzotti reaction: In onchocerciasis patients, adverse reactions correlate with pretreatment microfilarial counts rather than concurrent intestinal parasitic infections 4

Special Populations and Precautions

Pregnancy

  • Category C: Teratogenic in animal studies at doses higher than those used in humans
  • Not recommended during pregnancy unless benefits outweigh risks 1

Breastfeeding

  • Excreted in human milk in low concentrations
  • Treatment should only be undertaken when benefits outweigh risks 1

Pediatrics

  • Safety not established in children weighing less than 15 kg 3, 1

Elderly

  • Use caution due to potential decreased hepatic, renal, or cardiac function 1

Important Precautions

  1. Loa loa co-infection: Patients with onchocerciasis who are also heavily infected with Loa loa may develop serious or fatal encephalopathy following treatment 1

  2. Blood-brain barrier: Ivermectin does not readily cross the blood-brain barrier in humans, contributing to its safety profile 1

  3. Drug interactions:

    • May increase INR when co-administered with warfarin
    • P-glycoprotein inhibitors may increase neurotoxicity 1, 5
  4. Administration: Should be taken on an empty stomach with water for optimal absorption 1

Efficacy for Parasitic Infections

  • Strongyloidiasis: 64-100% cure rate following a single 200 mcg/kg dose 1
  • Onchocerciasis: 83.2% decrease in skin microfilariae count 3 days post-treatment and 99.5% decrease after 3 months 1
  • Scabies: Highly effective, particularly for crusted scabies 3
  • Other parasites: Shows activity against Ascaris lumbricoides and some protozoal infections 4, 6, 7

Follow-up Recommendations

  • For strongyloidiasis: At least three stool examinations over three months following treatment to ensure eradication 1
  • For scabies: Retreatment 2 weeks after initial treatment if symptoms persist or live mites are observed 3
  • For onchocerciasis: Marked reduction maintained for up to 12 months after a single dose 1

Ivermectin has maintained an excellent safety record over more than 25 years of clinical use for parasitic infections when used according to FDA-approved guidelines and dosing recommendations.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Ivermectin: a mini-review.

Clinical toxicology (Philadelphia, Pa.), 2022

Research

The effect of ivermectin on Cryptosporidium parvum in experimentally infected rat.

Journal of the Egyptian Society of Parasitology, 2000

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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