DISCLAIMER:THIS PAGE IS NOT INTENDED TO BE MEDICAL ADVICE! It is infomation from various sources (as referenced), and may be formatted in a more understandable way.
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Doseage Calculator
Do NOT use the information on this page as medical advise!
CAUTION! If you have alpha-gal syndrome, CONSIDER WELL, NOT TAKING THE IVERMECTIN MENTIONED ON THIS PAGE!
It could be very dangerous to your health!
The data on this page is gathered from various sources and presented here for your use.
Propylene Glycol in an ingredient in the both products mentioned on this page, so if there is a chance you might have AGS, you should consider NOT taking these products just to get the Ivermectin
Please contact me if you find data that is incorrect.
Enter your weight in pounds in the yellow box. Then click (or tap) on the calculate button.
Dose Ratio mcg/kg
Weight in lbs.
Weight in kg
Dose in mcg
Dose in mg
Dose in ml
200
400
800
1200
Caution - The dosage in pink is not recommended without the advice of a doctor!
There are predominantly two dosage ratios (200mcg/kg and 400mcg/kg) mentioned in many papers3, 18, 43. The 200 mcg/kg is a prophylactic (intended to prevent disease) and the 400 mcg/kg is an aggressive dose intended to treat a disease. Note: mcg is micrograms.
The aggressive dose may be administered orally once per day for 4 days. The first daily dose will put a percentage of the peak level of that dose into your system within a few minutes. The level in your system will then decline. At about 18 hours the level in your system will decline to 50% of the peak dose, and will continue to decline until you take the next dose.
When you take the next dose, the same effect happens, but this time the peak dose will be added to the residual that is left in your system from the previous dose(s). This same thing will happen after each dose.
The limit of the peaks will be reached after the 4th dose, which should be your last dose of the "agressive" dosage for the week.
Drug Half-Life Calculator
Following is a Half-Life Calculator where you can enter your calculated dose (from above). Enter the half-life of Ivermectin (18 hours). Enter how often you wish to take the dose (agressive = every 24 hours, prophylactic = 168 hours).
Shop around and you can find IVM (Ivermectin) as low as $.02 USD per 12mg tablet.
Update: Contacted supplier in India and the cost for 1 box (200 12mg tablets) with shipping and customs would be $89.00 USD. That's more than my per dose cost.
Information About Ivermectin
CDC says it should be used for scabies and worms.1
Nobel prizes awarded for discovery and practical use of Ivermectin. 12, 40
South Carolina Dept. of Health tries to bury the truth of Ivermectin. 39
2023 study finds IVM not effective as COVID treatment45
2019 FDA approved 1% Ivermectin for treatment of rosacea in adults.53, 54,
2024 Ivermectin shows promise of improved Covid survival rates.56
2024 Ivermectin may have therapeutic benefits for IPF.58
2023 Eprinomectin: a derivative of ivermectin suppresses growth and metastatic phenotypes of prostate cancer cells59
2023 FDA capitulates on some Ivermectin positions and comments60
2021 Ivermectin is known to inhibit the replication of flavivirus.61
2019 Significant reduction in bed bug population after insects feed on blood of person that has taken only 1 dose of Ivermectin.62
2024 Mosquitocidal effect of ivermectin-treated nettings and sprayed walls on Anopheles gambiae s.s.63
2011 Ivermectin, ‘Wonder drug’ from Japan: the human use perspective.64
2022 Usual safe medication doses of Ivermectin drug in human beings is 0.2–0.4 mg/kg.65
2014 Severe clinical manifestation of demodex mites may require Ivermectin.67
Experiences with Ivermectin
Personal
After the first dose, I experienced slight symptoms of vertigo and a short period (about an hour) of very slightly blurred vision (not anywhere near like removing my glasses).
Dose 2, 3 and 4 on days 2, 3 and 4, each precipitated similar vertigo symptoms, although with shorter and less intense symptoms each successive day.
My 5th dose was taken 168 hours (1 week) after number 4 dose and there were no side effects experienced.
Dose #6 was taken 168 hours after dose #5. No side effects noted.
Case studies
Report of DRESS symptoms5. This report warrants discussion and investigation into the "what" was going on, and "why" was it happening. When there are just a few cases like this, after over 2 billion administrations of Ivermectin, they need to be thouroughly understood.
We showed that ivermectin administration was associated significantly with lower mortality among patients with COVID-19, particularly in patients with more severe pulmonary involvement.
This study was conducted in healthy adult volunteers in which we compared 3 treatment regimens: the weight-based reference standard versus 2 experimental regimens of fix-dose 18 and 36 mg using 18 mg tablets. All 54 volunteers received the 3 treatments sequentially. The results confirmed that the fixed-dose regimen (both 18 mg and 36 mg) are as safe as the standard dosage and could justify the use of fix dosing regimens rather than the current weight based strategy.
Here we show that ivermectin also inhibits infection of epithelial cells by the bacterial pathogen, Chlamydia trachomatis, at doses that could be envisioned clinically for sexually-transmitted or ocular infections by Chlamydia.
For use in humans as an anti-helminthic, ivermectin is typically received orally at a dose of 150 µg/kg body weight, and peak plasma concentrations from such dosage reach around 60 nM
The plasma levels for patients, after 5.2 hours, peaked at 52.0 ng/ml. The elimination half life was 35.0 h;Note: This does not match the accepted HL of 18 hours and the area under the plasma concentration curve versus time, 2852 ng.h.ml-1. In healthy volunteers, the plasma ivermectin distribution was similar to that in patients, and both groups showed a tendency for a second rise in plasma concentration of the drug suggestive of enterohepatic recirculation. Ivermectin was detected in tissues obtained from patients. Fat showed the highest and most persistent levels, whilst values for skin, nodular tissues, and worms were comparable. Subcutaneous fascia contained the lowest concentrations.
Survival of malaria transmitting Anopheles mosquitoes is strongly decreased after feeding on humans recently treated with ivermectin. Currently, mass drug administration of ivermectin is under investigation as a potential novel malaria vector control tool to reduce Plasmodium transmission by mosquitoes. A "post-ivermectin effect" has also been reported, in which the survival of mosquitoes remains reduced even after ivermectin is no longer detectable in blood meals.
A fancy title to say: How to safely use Ivermectin to control mosquitos.
In humans, studies with radio-labelled ivermectin show that peak plasma concentration of metabolites is about twice that of the parent drug and occurs later, at 7 h (vs four for parent drug). Plasma metabolites are less polar than the parent drug and could be fatty acid ester conjugates of the monosaccharides or aglycone of the parent drug.
The plasma half-life of metabolites is about 72 h, fourfold that of the parent drug.
Ivermectin’s impact on mosquito mortality is directly related to the time there is a lethal concentration in the blood
The longer the drug remains in the blood, the more mosquitoes it will kill or disable. Any increase in duration of mosquitocidal concentrations is expected to contribute to additional mortality. Modelling shows that the time the drug remains in blood above mosquito-killing levels is the parameter that drives impact on transmission [50].
Abstract:
Ivermectin was used for the treatment of a scabies outbreak in a nursing home. Among the 128 residents, 42 presented pruritus or cutaneous lesions and scabies was parasitologically demonstrated in seven patients. All residents were treated with two 12 mg doses of ivermectin given two weeks apart. Ivermectin treatment associated with procedures for environmental disinfection led to the control of the outbreak. In only one case, was there a failure of the treatment. It is concluded that oral ivermectin is an effective and practical therapy for scabies in nursing homes.
The highest dose of ivermectin that we have used in our study is 12 mg (200 µg/kg) once daily for 5 consecutive daysNote: This dose is calculated for a 133 pound person., which resulted in a significantly shorter time for viral clearance. Viral clearance was earlier in the 5-day ivermectin treatment arm when compared with the placebo group (9.7 days vs 12.7 days; p = 0.02), but this was not the case for the ivermectin + doxycycline arm (11.5 days; p = 0.27). Similarly, clinical trials with a 3-day, once-daily dose of 400 µg/kg oral ivermectin in dengue patients has been shown to be safe, with accelerated clearance of the dengue virus nonstructural protein 1
After analyzing the results of the different clinical trials it is concluded that the use of ivermectin in combination with doxycycline can prove to be an effective, safe and affordable therapeutic regimen for relieving the cytokine storm of COVID-19 infection.
Two-dose ivermectin prophylaxis at a dose of 300 µg/kg with a gap of 72 hours was associated with a 73% reduction of SARS-CoV-2 infection among healthcare workers for the following month. Chemoprophylaxis has relevance in the containment of pandemic.
FDA-approved anti-parasite drug ivermectin is also an antibacterial, antiviral, and anticancer agent, which offers more potentiality to improve global public health, and it can effectively inhibit the replication of SARtarget="_blank"S-CoV-2 in vitro
The findings in this study demonstrate the broad-spectrum antiviral property of ivermectin benefiting for COVID-19 treatment in the context of predictive, preventive, and personalized medicine in virus-related diseases.
Viruses mentioned:
HCMVMayo,
HPVMayo,
EBVVWH, and
HIV-1NIH
There is a relative dirth of studies regarding Clorsulon: A site:nih.gov search shows 905 vs 35,800 for ivermectin.
This is a sheep & goat study that speaks to some questions regarding Clorsulon.: After a single dose of 7 mcg/kg, peak plasma consentration @ 14h (goats) 15h (sheep). There's more in the abstract.
It was considered that the absence of burrows, eggs and mites did not eliminate the risk of scabies infestation. Ivermectin (Maruho Co., Ltd., Osaka, Japan) was administered orally as therapeutic administration (200µg/kg twice at two-week intervals) in 6 patients and as a preventive (one dose of 200µg/kg) in 35 individuals.
Sulfonamide antibiotic reactions encompass the entire spectrum of 4 types of hypersensitivity reactions.
Type 1 hypersensitivity is IgE-mediated and may include an anaphylactic sequelae. (Interpretation: Anaphylactic shock is possible.)
Type 2 reactions involve antibody-mediated cytotoxic cellular injury that may result in various cytopenias. (Interpretation: A soldier of your immune system targets an undesirable cell, then attacks it, glues itself to the enemy cell, then destroys it. Cytopenia means the attack is now destroying even your red blood cells.)
Type 3 and type 4 hypersensitivity results in the formation of antigen–antibody immune complexes or a delayed T cell-mediated reaction, respectively, either of which may progress to the life-threatening Stevens-Johnson syndrome or toxic epidermal necrolysis. (Interpretation: Your immune system goes into tornado mode and starts destroying anything that it thinks could possibly be an enemy cell, even to the point of killing the host body.)
I believe the conclusion of this study should be challenged. Is it more likely this woman suffered an anaphlyactic response to the Clorsulon, possibly exacerbated by an eosinophil storm, described as a DRESS event?
My Question: Because Clorsulon is a sulfonamide, is it possible a hypersensitivity reaction was triggered?
Yes, because Clorsulon is a sulfonamide, it is possible that a hypersensitivity reaction could be triggered. Sulfonamide antibiotics are known to cause a variety of hypersensitivity reactions, ranging from benign rashes to severe cutaneous adverse reactions like Stevens-Johnson syndrome and toxic epidermal necrolysis. The potential for hypersensitivity reactions with sulfonamides is well-documented, with an incidence of adverse reactions in approximately 3% of the general population, and much higher in patients with conditions like HIV. While Clorsulon is primarily used as an antiparasitic agent, its sulfonamide structure means it shares common characteristics with sulfonamide antimicrobials, which could theoretically lead to cross-reactivity in individuals with a history of sulfonamide hypersensitivity. However, specific data on Clorsulon's hypersensitivity potential might be less extensive since it is not as widely used or studied as some other sulfonamide drugs.nih-1, sci-1
Treatment with topical ivermectin 10 mg/g (1%) cream once daily resulted in an almost complete clinical resolution after 15 days [Figure - 4], but direct microscopy was still positive. Maintenance of the treatment for 2 months led to clinical and direct microscopic clearance at follow-up visit, with no relapses in the following 6 months.
Ivermectin promotes wound healing partly through modulation of the inflammatory process and the levels of Transforming Growth Factor-Beta 1 and Vascular Endothelial Growth Factor. Low doses of ivermectin cream have the potential to be used in treating wounds with minimal scar tissue formation.
The aims of this study are to determine the prevalence of
cattle ringworm in native dairy farms of Diyala governorate, and the
distribution of T. verrucosum and treatment of the infection in the bovine by
ivermectin
Results: Statistical analysis reveals significantly less clearance time (50%) when ivermectin is used instead of topical antifungal 1% sulpher ointment in treating the disease. With less time of 13-24 days compared to 30-40 days. The treatment of ringworm disease in cattle with clearance rate of 100% is achieved using Ivermectin.
Ivermectin as a treatment for SARS-CoV-2 in humans has already been approved in a number of states and countries, including the Republic of Peru [44] and Northeastern Beni region of Bolivia [45]. Importantly, close to 70 trials worldwide are currently testing the clinical benefit of ivermectin to treat or prevent SARS-CoV-2 (see Table 3)
Ivermectin as a treatment for SARS-CoV-2 in humans has already been approved in a number of states and countries, including the Republic of Peru [44] and Northeastern Beni region of Bolivia [45]. Importantly, close to 70 trials worldwide are currently testing the clinical benefit of ivermectin to treat or prevent SARS-CoV-2 (see Table 3);
What does "host-directed" really mean? It means the therapy (in this case, Ivermectin) is directed at the host (you), in order to change the environment in which a virus in located. This makes the host an inhospitable place to live and inhibits its ability to replicate.
Starting in 2012, ivermectin’s antiviral properties have been progressively documented towards a number of RNA viruses, including human immunodeficiency virus (HIV)-1, influenza, flaviruses such as dengue and Zika, and most notably, SARS-CoV-2 (COVID-19)
4,
5,
7,
8,
9,
10,
11,
12,
13,
14,
15,
16,
17,
as well as DNA viruses such as pseudorabies, polyoma and adenoviruses
18,
19,
20
Avermectin is a potent broad-spectrum parasiticidal drug, the discovery of which led to the award of the 2015 Nobel Prize in physiology or medicine. Its derivative, ivermectin, has recently been reported to be a potential anticancer agent against colon cancer, ovarian cancer, melanoma, and leukemia. Our recent study demonstrates that ivermectin also exerts a promising anticancer effect for breast cancer as evidenced by marked growth inhibition after 24-h treatment with ivermectin in a range of breast cancer cell lines, with no obvious effects on nontumorigenic human breast cells. The anticancer activity of ivermectin was further confirmed in both mouse subcutaneous xenografts and orthotopic breast cancer models.
Case Study: Patient was diagnosed as having crusted scabies with bullous pemphigoid-like eruptions and nail involvement
prescribed oral ivermectin (two doses of 12 mg ivermectin with a 1-week interval) and topical lindane (1%gamma-BHC in petrolatum) for scabies with 5% salicylic acid in plastibase as an additional treatment for the crusted lesions on his soles. He showed remarkable improvement in 2 weeks, and his nails showed complete recovery after 7 weeks of occlusive dressing treatment with 1%gamma-BHC.
The bullous symptoms of this patient were considered to be due to the scabies, because the patient recovered completely after receiving treatment for scabies. Indirect immunofluorescent study is important to distinguish between scabies with blister formation and true bullous pemphigoid.
Question: Does ivermectin, with a maximum targeted dose of 600 µg/kg daily for 6 days, compared with placebo, shorten symptom duration among adult (=30 years) outpatients with symptomatic mild to moderate COVID-19?
Conclusions and Relevance: Among outpatients with mild to moderate COVID-19, treatment with ivermectin, with a maximum targeted dose of 600 µg/kg daily for 6 days, compared with placebo did not improve time to sustained recovery. These findings do not support the use of ivermectin in patients with mild to moderate COVID-19.
Our findings demonstrate the anticancer effect of ivermectin in prostate cancer, indicating that its use may be a new therapeutic approach for prostate cancer.
Report of a rare case of massive orbital myiasis (fly maggots) following recent lid injury, occurring in the empty socket of an elderly lady, who had concurrent scalp pediculosis (lice). The orbital myiasis was effectively treated with the broad-spectrum antiparasitic agent, ivermectin, thus precluding the need for an exploratory surgery. Ivermectin was also effective in managing the concurrent scalp pediculosis.
A single oral dose of ivermectin was generally effective for the treatment of head lice, especially when used in combination with a LiceMeister® comb and when the whole family was treated. About 15% of patients required a second dose 24 h after the first.
Ivermectin has significant antiarthritic properties and can be a novel treatment agent for the management of rheumatoid arthritis patients suffering from strongyloidiasis.
The conclusion of this study begs the question: Why for strongyloidiasis patients and not others?
Unique method of measuring plasma levels of Ivermectin. Describing the dosing usefully i.e. mg/kg and describing the plasma and fecal concentrations usefully i.e. ng/ml.
The study was conducted in a manner which eliminates many biological variables.
Topical ivermectin is an effective treatment for inflammatory papulopustular rosacea in adults. Positive therapeutic effects of ivermectin due to its potential anti-inflammatory properties could be achieved in the other facial dermatoses.
In December 2014, the US Food and Drug Administration approved 1% ivermectin cream for treatment of rosacea in adults while the first European approval was obtained in March 2015.
Herein, we report the pharmacological effects and targets of ivermectin in prostate cancer.
Recently, several studies have explored the potential of ivermectin as a new cancer treatment nih-2,nat-1,nat-2
In breast cancer, ivermectin decreases p21-activated kinase 1 (PAK1) expression by promoting its degradation and inducing cell autophagy [aacrj-1]
In ovarian cancer, ivermectin can block the cell cycle and induce cell apoptosis through a Karyopherin-β1 (KPNB1) related mechanism [pnas-1].
In leukemia, ivermectin preferentially kills leukemia cells at low concentrations by increasing the influx of chloride ions into cells, which triggers plasma membrane hyperpolarization and reactive oxygen species (ROS) production [cas-1]
The study showed that higher neutrophil levels were linked to mortality in tocilizumab-treated patients, while ivermectin showed promise in increasing survival rates.
This study indicate that ivermectin may have therapeutic benefits for IPF, likely due to its ability to reduce inflammation and mitigate oxidative stress-induced toxicity.
Retire FDA’s Consumer Update entitled, Why You Should Not Use
Ivermectin to Treat or Prevent COVID-19, originally posted on March 5,
2021, and revised on September 7, 2021 (ECF No. 12, Ex. 1), while
retaining the right to post a revised Consumer Update.
Delete and not republish
(1) FDA’s Twitter, LinkedIn, and Facebook posts from August 21, 2021 (ECF No. 12, Exs. 4, 5), that read, “You are not a horse. You are not a cow. Seriously, y’all. Stop it.”;
(2) FDA’s Instagram post from August 21, 2021 (ECF No. 12, Ex. 6), that reads, “You are not a horse. Stop it with the #ivermectin. It’s not authorized for treating #COVID.”
(3) FDA’s Twitter post from April 26, 2022 (ECF No. 12, Ex. 7), that reads, “Hold your horses, y’all. Ivermectin may be trending, but it still isn’t authorized or approved to treat COVID-19.”
(4) all other social media posts on FDA accounts that link to Why
You Should Not Use Ivermectin to Treat or Prevent COVID-19 (ECF No. 12,
Ex. 1).
IVM not only has strong effects on parasites but also has potential antiviral effects. IVM can inhibit the replication of flavivirusCDC-1 by targeting the NS3 helicase
Objective: To measure the population size and fecundity (ability to reproduce) of the common bed bug after feeding it with the blood obtained from human subjects who have consumed a single dose of ivermectin.
Conclusions: There were significant reductions in bed bug population size and fecundity in insects that fed on blood obtained from human study subjects up to 96 hours after they have consumed a single oral dose of ivermectin.
Ivermectin (IVM) has been proposed as a new tool for malaria control as it is toxic on vectors feeding on treated humans or cattle.
IVM may have a direct mosquitocidal effect when applied on bed nets or sprayed walls.
The potential for IVM application as a new insecticide for long-lasting insecticidal nets (LLINs) and indoor residual spraying (IRS) was tested in this proof-of-concept study in a laboratory and semi-field environment.
The results showed a direct mosquitocidal effect of IVM on this mosquito strain as all mosquitoes died by 24 h after exposure to IVM.
Subjects received oral doses of 30 to 120 mg (333 to 2000 mcg/kg) ivermectin in a fasted state or 30 mg (333 to 600 mcg/kg) ivermectin following a standard high-fat (48.6 g of fat) meal
Administration of 30 mg ivermectin following a high-fat meal resulted in an approximate 2.5-fold increase in bioavailability relative to administration of 30 mg ivermectin in the fasted state.
Significant lethality was observed in mice and rats after single oral doses of 25 to 50 mg/kg and 40 to 50 mg/kg, respectively. No significant lethality was observed in dogs after single oral doses of up to 10 mg/kgNote: These are more than 100 times the recommended dose.
After clinical manifestations (of demodex mites), the mites may be temporarily eradicated with topical insecticides, especially crotamiton cream, permethrin cream, and also with topical or systemic metronidazole. In severe cases, such as those with HIV infection, oral ivermectin may be recommended.
Colonization of the skin with Demodex could be a reflection of immune response of the host to organism.
Drug repositioning( SD1)Drug repurposing (DR), also known as drug repositioning or re-profiling, is an approach to identify new therapeutic indications (other than original indications) of an already approved drug.
is defined as a process to identify a new application for drugs.
In 2018 there were 18.1 million new cancer cases. There were also 9.6 million cancer deaths that year.
The development of a new drug takes 10–15 years, and the success rate is negligible (approximately 2%).
There are seven classes of modern anthelmintics
Ivermectin, as a member of MLs, is metabolized in the liver by the cytochrome P450 system. The blood concentration of the drug reaches the peak 4 h after administration, and after that, the concentration decreases slowly. The metabolites concentration in the blood increases for a longer time when it is compared with the parent compound, which can be resulted from the heterohepatic recycling. The drug can be detected in various sites, including the nodules, and subcutaneous fascia. A single oral dose (12 mg) of ivermectin reaches the peak 8 h after administration in various sites, such as sebum, and forehead, and starts to decrease after 24 h
Ivermectin, a US Food and Drug Administration-approved anti-parasitic agent, was found to inhibit severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) replication in vitro.
A randomized, double-blind, placebo-controlled trial was conducted to determine the rapidity of viral clearance and safety of ivermectin among adult SARS-CoV-2 patients.
The trial included 72 hospitalized patients in Dhaka, Bangladesh, who were assigned to one of three groups:
Oral ivermectin alone (12 mg once daily12 mg once daily is considered the minimal effective prophylactic dose for a person who weighs 133 pounds (see the dosage calculator on this page).
Dosage Calculator for 5 days)
Oral ivermectin in combination with doxycycline (12 mg ivermectin single dose and 200 mg doxycycline on day 1, followed by 100 mg every 12 h for the next 4 days)
A placebo control group.
Clinical symptoms of fever, cough, and sore throat were comparable among the three groups.
Virological clearance was earlier in the 5-day ivermectin treatment arm when compared to the placebo group (9.7 days vs 12.7 days; p = 0.02), but this was not the case for the ivermectin + doxycycline arm (11.5 days; p = 0.27).
There were no severe adverse drug events recorded in the study.
A 5-day course of ivermectin was found to be safe and effective in treating adult patients with mild COVID-19.
The antiparasitic drug, ivermectin (IVM), exerts anticancer activities in diverse cancer types. However, its anticancer activity against cholangiocarcinoma (CCA), especially the drug-resistant phenotype, has not yet been explored.
IVM was tested for its anticancer activity against gemcitabine-sensitive (KKU214) and gemcitabine-resistant (KKU214GemR) CCA cell lines.
IVM treatment inhibited cell proliferation and colony formation of both KKU214 and KKU214GemR in a dose- and time-dependent manner.
Ivermectin, an FDA-approved anti-parasitic drug, effectively inhibits infection with hepatitis E virus (HEV) genotypes 1 and 3 in a range of cell culture models, including hepatic and extrahepatic cells.
Long-term treatment showed no clear evidence of the development of drug resistance.
Gene silencing of importin-α1, a cellular target of ivermectin and a key member of the host nuclear transport complex, inhibited viral replication and largely abolished the anti-HEV effect of ivermectin. What does this mean?The statement indicates that importin-α1 is vital for HEV replication. Ivermectin targets this protein to inhibit viral replication. However, if importin-α1 is silenced (its expression is reduced or eliminated), HEV replication decreases, but so does ivermectin's ability to fight the virus because it can no longer interact with this key protein in its mechanism of action.
Infection with yellow fever virus (YFV), the prototypic mosquito-borne flavivirus, causes severe febrile disease with haemorrhage, multi-organ failure and a high mortality.
Ivermectin, a broadly used anti-helminthic drug, proved to be a highly potent inhibitor of YFV replication (EC50 values in the sub-nanomolar range).
Moreover, ivermectin inhibited, although less efficiently, the replication of several other flaviviruses, i.e. dengue fever, Japanese encephalitis and tick-borne encephalitis viruses.
Considering that this well tolerated drug has been licensed for >20years for the treatment of parasitic infections in man, our results provide the prospect of the first specific anti-flavivirus therapy by the off-label use of ivermectin (patent application EP2010/065880).
Ivermectin has not been approved by the FDA for use on flaviviruses. Ivermectin is FDA-approved for certain parasitic infections in humans, including strongyloidiasis and onchocerciasis, and for various external parasites like head lice when used topically. However, it has not received FDA approval for treating or preventing infections caused by flaviviruses, which include viruses like Dengue, Yellow Fever, West Nile, and Zika.
Several studies have explored ivermectin's potential antiviral effects against flaviviruses:
In vitro studies have shown that ivermectin can inhibit the replication of flaviviruses like Dengue, Yellow Fever, and West Nile by specifically targeting their NS3 helicase activity, suggesting potential antiviral effects.
Despite these findings, there's a lack of clinical data supporting ivermectin's efficacy against flaviviruses in human patients, and the FDA has not authorized or approved ivermectin for this use.
The discussion around ivermectin's use for various viral infections, including those by flaviviruses, remains largely in the realm of research and has not transitioned to FDA-approved applications for these purposes. The FDA's stance on ivermectin primarily relates to its use in parasitic infections, not viral ones, and any off-label use would not constitute formal FDA approval.