How should ivermectin be dosed for parasitic infections versus off-label uses like COVID-19?

Checked on December 5, 2025
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Executive summary

For approved parasitic infections, ivermectin is dosed by weight most commonly at about 150–200 micrograms per kilogram (μg/kg) as a single oral dose (strongyloidiasis typically 200 μg/kg; onchocerciasis often 150–200 μg/kg), with some indications (lymphatic filariasis) using higher regimen strategies (400 μg/kg in mass programs) and repeat doses as clinically required [1] [2] [3]. By contrast, major health authorities and randomized trials show no established, regulatory-approved dose for COVID‑19 — trials have tested higher regimens (for example 400 μg/kg daily for 3 days) but systematic reviews and public-health statements conclude ivermectin is not proven effective for COVID‑19 and warn against using veterinary formulations or unapproved high doses [4] [5] [6] [7].

1. What standard, evidence-based dosing looks like for parasitic disease

Ivermectin dosing for human parasitic infections is weight‑based and short-course: the standard, FDA‑label and guideline doses are in the 0.15–0.20 mg/kg (150–200 μg/kg) range given orally as a single dose for strongyloidiasis and onchocerciasis, with follow-up or repeat treatment in some settings; tablets are commonly 3 mg and taken on an empty stomach [2] [3] [8]. Scabies and some ectoparasite uses employ 200 μg/kg with repeat dosing after 7–14 days or multiple doses for crusted scabies as recommended by dermatology and public‑health sources [9] [10]. Mass‑drug‑administration programs and specialty protocols sometimes use higher aggregate regimens for filarial control, and there is long safety data around these parasitic regimens [11] [1].

2. Why dosing is weight‑based and why formulations matter

Clinical sources repeatedly emphasize dosing by micrograms per kilogram to ensure efficacy and safety; ivermectin tablets are manufactured for human use (e.g., 3 mg tablets) and patients must not substitute veterinary products because animal formulations and much larger doses can be toxic to humans [1] [3] [8] [6]. Clinical guidance stresses follow‑up testing (for Strongyloides, stool exams) because a single dose is effective but does not eliminate adult Onchocerca worms, so retreatment and monitoring are part of standard care [3] [12].

3. The off‑label COVID‑19 claims and the trial evidence

Interest in ivermectin for COVID‑19 led to multiple randomized trials and reviews. Large randomized trials have tested higher or repeated dosing — for example, a trial administered 400 μg/kg once daily for 3 days — but the best available aggregate evidence and systematic reviews find no robust mortality or viral‑clearance benefit; several reviewers conclude ivermectin is ineffective for COVID‑19 management and public‑health bodies do not approve any dose for SARS‑CoV‑2 [4] [5] [13]. Importantly, the dose used in parasitic disease (150–200 μg/kg single dose) is not supported as an effective antiviral dose by trials and meta‑analyses [5] [4].

4. Safety tradeoffs when increasing dose or using non‑standard regimens

Higher or prolonged ivermectin dosing has been explored in research (dose‑finding trials and malaria transmission studies) and in some COVID‑19 trials, but increased doses raise risks: neurotoxicity, gastrointestinal symptoms, and other adverse events have been reported with overdoses or inappropriate products; animal doses are dangerous for humans and regulatory agencies have warned against self‑medication with veterinary ivermectin [11] [6] [14]. The therapeutic window used for parasitic indications has decades of safety data when prescribed and monitored [11] [10].

5. How clinicians and public health bodies frame “off‑label” use

Off‑label prescribing is legally possible but must be grounded in evidence, risk–benefit judgment and informed consent. For parasitic infections, off‑label variants (e.g., repeated dosing for scabies) are supported by clinical practice sources [9] [10]. For COVID‑19 and other proposed uses (cancer, antiviral prophylaxis) the dominant message from clinical reviews and public‑health reporting is that evidence is inadequate or negative and regulators have not approved ivermectin for viral indications [5] [13] [6].

6. Practical guidance for patients and clinicians

If treating a confirmed parasitic infection, prescribe human‑formulation ivermectin at guideline weight‑based doses (commonly 150–200 μg/kg single dose; specific regimens vary by parasite) and perform indicated follow‑up testing [2] [3]. For COVID‑19 or other non‑parasitic uses, follow randomized‑trial evidence and public‑health guidance: randomized trials have not demonstrated a clear benefit, higher experimental doses have been tested but are not approved, and authorities warn against self‑treating with veterinary products [4] [5] [6]. Available sources do not mention an FDA‑approved ivermectin dose for COVID‑19.

Want to dive deeper?
What are the approved ivermectin dosing guidelines for common parasitic infections in adults and children?
How does veterinary ivermectin differ in formulation and potency from human ivermectin and why is that important?
What evidence and clinical trial results exist on ivermectin's efficacy and safety for COVID-19 treatment or prevention as of 2025?
What are the known risks, drug interactions, and toxicity signs of ivermectin overdosing in humans?
How do regulatory agencies (FDA, EMA, WHO) currently recommend use of ivermectin for parasitic diseases versus off-label COVID-19 use?