Ketrax

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Ketrax

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Medically reviewed

Rosario Oropesa

Last updated on 22/12/2025

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

Overview of Ketrax

Quick Facts

Property Description
Active ingredient Levamisole, Levamisole Hydrochloride
Form Tablet, Oral Solution
Pharmacological class Anthelmintic agent, Immunomodulator
Common use Eliminating parasitic worm infections
Origin Synthetic compound (Imidazothiazole derivative)

What is Ketrax and its Core Composition?

Ketrax is the medicinal preparation containing the core active substance, Levamisole Hydrochloride (INN: Levamisole). This compound is formally defined as a synthetic imidazothiazole derivative and is not derived from natural sources. Levamisole is included in the World Health Organization's List of Essential Medicines for its primary therapeutic role. The drug is primarily manufactured as a single product and is formulated for oral administration, typically available as a Tablet or an Oral Solution. The formulation as the Hydrochloride salt ensures optimal water solubility for rapid absorption from the gastrointestinal tract, a key feature that is clinically recognized for facilitating quick action against target organisms.

What Pharmacological Class Does Levamisole Belong To?

Levamisole belongs to the pharmacological class of Anthelmintic agents, targeting parasitic infections, specifically those caused by nematodes (roundworms). However, the substance is characterized by a critical dual classification, also acting as an Immunomodulator. This dual nature indicates that the medicine has potential benefits related to supporting and balancing the body's immune system, in addition to its primary anti-parasitic function. This unique dual mechanism distinguishes it from anti-parasitic agents that operate solely through metabolic interference. The general purpose of Ketrax is derived from this profile: its primary function is the swift elimination of targeted helminths, which makes it particularly useful in clearing the entire parasitic burden. Concurrently, the immunomodulatory properties mean the medicine is uniquely capable of addressing clinical needs where the restoration or enhancement of depressed host immune responses is a necessary therapeutic component.

Regulatory References

  1. National Cancer Institute Drug Dictionary: Levamisole
  2. WHO Essential Medicines List: Levamisole

What side effects are possible with Ketrax?

Possible Side Effects and Safety Information

The safety profile of Ketrax (Levamisole) is documented by regulatory authorities, classifying possible effects by frequency and the body system affected. Officially listed adverse reactions are grouped into several System-Organ Classes, including Gastrointestinal Disorders (Nausea, Diarrhea, Vomiting, Stomatitis), Nervous System Disorders (Headache, Dizziness, Paresthesia), and Skin and Subcutaneous Tissue Disorders (Skin rash, Dermatitis, temporary Alopecia).

Serious Adverse Reactions

Official documents highlight rare but serious adverse reactions that are primarily associated with the drug's immunomodulatory use or repeated dosing regimens, rather than single anthelmintic doses. The most critical concerns are related to the blood and nervous systems. These include potentially fatal conditions such as Agranulocytosis (a severe reduction in white blood cells) and serious Neurotoxicity, notably Leukoencephalopathy (an encephalopathy-like syndrome).

Other serious reactions listed are Vasculitis (inflammation of blood vessels) and severe skin reactions like Stevens-Johnson Syndrome.

Safety Considerations and Limitations

Safety restrictions are documented for certain populations. The medicine is contraindicated in individuals with a known hypersensitivity to Levamisole or with pre-existing blood disorders. Caution is advised for patients with a history of hepatic or renal impairment. Furthermore, regulatory texts note that the risk of Agranulocytosis has a significantly higher incidence when associated with repeated high doses over extended periods. Because of potential disulfiram-like effects, the consumption of alcohol is prohibited during the treatment period and for at least 24 hours following intake.

These official classifications define the medicine's risk profile, focusing attention on hematologic and neurological monitoring, and guide its appropriate use based on patient history and co-ingestion restrictions.

Overdose and Emergency Response

Overdose and when to seek help

The following information details the officially documented signs of Ketrax (Levamisole) overdose and the emergency actions mandated by regulatory authorities.

Overdose scope

Documented Overdose Presentations Physiological Systems Affected When Immediate Medical Help is Required
Nausea, vomiting, increased salivation, colic, diarrhea, dizziness, headache, anxiety, muscle tremors, hyperesthesia, ataxia, depression, prostration, collapse, and clonic convulsions. Gastrointestinal, Neurological, Respiratory, Autonomic, Motor. When overdose is suspected or known, seek medical advice immediately.

Overdose Classifications (High-Level)

Severity Classification (as defined in official documents) Emergency-Response Statements Supportive and Antidote Information
The immediate cause of death in severe poisoning is documented as asphyxia due to respiratory failure. The mandated action is to seek medical advice immediately. The guidance also states to DO NOT induce vomiting as a standard first aid measure. Management is required to be symptomatic and supportive. No specific antidote is officially known, though Atropine sulfate can be used to alleviate certain clinical signs.

Official Overdose Statements

Official regulatory sources define the overdose scenario by the onset of a specific cluster of systemic and neurological signs. The severe clinical presentation may include seizures, collapse, and the life-threatening risk of respiratory failure, which necessitates immediate medical intervention. The required emergency action is to seek medical advice immediately and, crucially, the treatment approach is defined as symptomatic and supportive, acknowledging the absence of a specific named antidote. Patients with a history of liver or kidney diseases are noted to have a potential for increased severe adverse effects.

This structure ensures that the overdose profile and the conditions under which urgent help must be sought are based strictly on regulatory-mandated text.

Therapeutic Uses of Ketrax

What Ketrax treats: main uses and benefits

Ketrax is an anthelmintic medication primarily used to treat infections caused by specific types of parasitic worms. Its active mechanism focuses on neutralizing parasites to assist the body in clearing the infection.

Primary Indications

The medication is most commonly utilized for the treatment of common intestinal parasitic conditions, including:

  • Ascariasis: Infections caused by large roundworms (Ascaris lumbricoides).
  • Hookworm infections: Treatment of infections resulting from Ancylostoma duodenale or Necator americanus.

Therapeutic Benefits

The primary benefit of Ketrax is its ability to paralyze the musculature of susceptible parasites. This action prevents the worms from maintaining their position within the host's digestive tract, allowing them to be expelled naturally through intestinal movement.

By addressing the underlying parasitic load, the medication helps to:

  • Reduce parasite-related complications: Lowering the risk of intestinal blockage or nutritional deficiencies often associated with heavy worm burdens.
  • Improve nutritional status: Reducing the competition for nutrients between the host and the parasites, which is particularly significant in pediatric cases.
  • Support gastrointestinal health: Clearing the infection helps resolve symptoms such as abdominal discomfort and irregular bowel activity caused by the presence of worms.

Eligibility and Restrictions for Use

Official Eligibility and Contraindications

Ketrax (Levamisole) is approved for use in adults and children for the treatment of specific parasitic worm infections. Regulatory documents define eligibility primarily through absolute prohibitions and conditional restrictions.

Classification Population Status
Absolute Contraindication Patients with pre-existing blood disorders Must Not Use
Absolute Contraindication Patients with advanced liver or kidney disease Must Not Use
Absolute Contraindication Known hypersensitivity to Levamisole Must Not Use
Conditional Use Pregnant women Not Recommended unless Essential
Conditional Use Breastfeeding mothers Not Recommended unless Essential
Caution Required Non-advanced hepatic or renal impairment Use with Caution

The medicine is formally contraindicated in groups with severe organ dysfunction or hematological conditions. Use during pregnancy and lactation is not recommended unless a physician deems it essential, due to insufficient data on potential risk. Individuals with non-advanced liver or kidney impairment, or certain conditions like rheumatoid arthritis, are designated for use with caution.

What should I know about interactions with other medicines?

Interactions with Other Medicines and Products

This section outlines the drug and substance interactions officially documented in government regulatory sources for Levamisole (Ketrax).

Interaction Classification Interacting Substance/Product Official Regulatory Statement
Formal Prohibition Alcohol (Ethanol) Must be avoided. Co-ingestion is associated with the risk of a disulfiram-like adverse reaction, which is a required label caution.
Potentiation of Drug Effects Warfarin Has been reported to cause an increase in anticoagulant effects, specifically a potential marked elevation of the International Normalized Ratio (INR).
Potentiation of Drug Effects Phenytoin Co-administration may lead to increased plasma concentrations of this anticonvulsant medicine, necessitating awareness of potential toxicity.
Combination Therapy Risk Fluorouracil (5-FU) When used in combination for specialized therapies, a documented risk exists for a severe central nervous system syndrome, such as multifocal inflammatory leukoencephalopathy.
Exposure Modification Ivermectin, Albendazole Levamisole has been noted in pharmacological data to increase the bioavailability and systemic exposure of these co-administered anthelmintic agents.

The regulatory interaction profile requires strict adherence to avoidance rules for certain substances. The official documentation identifies potential pharmacokinetic and pharmacodynamic interactions that can lead to altered drug exposures and enhanced effects of co-administered medicines. No timing-based separation rules or specific population-dependent interaction cautions (e.g., heightened severity in hepatic impairment) are formally documented in the regulatory prescribing information.

Mechanism of Action

Ketrax (Levamisole) employs a dual mechanism of action, targeting both the parasitic organism and the host's immune system at the cellular level. This distinct approach establishes the drug's action by operating through two distinct pharmacodynamic mechanisms.


Anthelmintic Action: Targeted Neuromuscular Interference

This primary mechanistic domain involves Levamisole acting as a direct agonist (activator) at nicotinic acetylcholine receptors ( nAChRs) specific to the susceptible parasites . This sustained overstimulation leads to a functional depolarizing neuromuscular blockade, rapidly causing spastic paralysis of the worm's musculature. This physical incapacitation is the key physiological consequence leading to the loss of GI wall attachment.


Immunological Pathway Modulation

The drug also operates in a secondary domain by functioning as a non-specific immunomodulator. It supports the activity of key host defense cells, including T-lymphocytes and phagocytes (macrophages and neutrophils), particularly in contexts where their function is suppressed. This mechanism modulates the cellular immune response, influencing the activity profile of host defense cells.

Dosage and Administration Information

How to Use Ketrax — Official Administration Guidelines

The usage of Ketrax (Levamisole) follows distinct, standardized protocols depending on the context, primarily as an anthelmintic agent or for its historically documented cyclic use as adjuvant therapy. Administration details follow established clinical application parameters.


Official Dosing and Scheduling

Usage Context Route and Form Standard Labeled Dose Duration and Frequency
Anthelmintic Oral (Tablet, Oral Solution) Adults: 150 mg as a single dose. Children: 2.5 mg/kg to 3 mg/kg body weight. Single Administration. May be repeated once after 7 days in cases of severe hookworm infection.
Adjuvant Therapy Oral (Tablet) 50 mg taken three times daily (total 150 mg per day). Administered for 3 consecutive days every 2 weeks, continuing for up to 1 year.

Administration Requirements

  • Method: Ketrax is administered exclusively by the oral route.
  • Timing: The medicine can be taken with or without food, although administration is suggested preferably after a light meal.
  • Dose Calculation: For pediatric anthelmintic use, the dose is weight-based (2.5 mg/kg or 3 mg/kg), requiring accurate body weight measurement for correct usage.
  • Missed Dose: For the cyclic adjuvant regimen, a missed dose should be skipped, and the patient should return to the regular schedule without doubling the subsequent dose.

These instructions define two separate and non-interchangeable procedures: a short-term, weight-based single-dose protocol and a long-term, cyclic treatment schedule.

Recent Clinical Evidence

Ketrax, which contains the active ingredient levamisole, is primarily recognized for its historical use as an antiparasitic medication to treat infections like ascariasis and hookworm. While its use has been withdrawn in some markets due to safety concerns, clinical research continues to investigate its potential applications and effects.


Studies in Oncology

Clinical trial data have explored levamisole's role as an adjuvant therapy in certain cancers, historically including colorectal carcinoma (Dukes' stage C). Evidence from specific trials supported its use in combination with the chemotherapy agent fluorouracil (5-FU) following surgical resection. This research suggested that its addition was associated with potential patient benefits in this specific setting. However, its use in oncology has largely been supplanted by newer agents and regimens, and trials in other cancers (e.g., advanced breast cancer, lung cancer) have been inconclusive.


Immunomodulatory and Emerging Research

Due to its established immunomodulatory properties—specifically the ability to influence T-cell function and monocyte/macrophage activity—levamisole has been the subject of research in various immune-mediated conditions.

Condition Studied
Nephrotic Syndrome (in children)
Loiasis (filarial infection)
Autoimmune disorders (e.g., rheumatoid arthritis)

Recent randomized, controlled trials have examined levamisole in the treatment of loiasis, suggesting that a multi-day regimen is associated with a greater reduction in the concentration of Loa loa microfilariae in the blood compared to placebo. Furthermore, studies exploring its immunomodulatory potential in other conditions, such as COVID-19 in specific patient cohorts, have shown associations with improved clinical status and reduced hospitalization time in small trials. However, these latter findings are limited and represent investigative uses outside of the established antiparasitic indication.

Frequently Asked Questions (FAQ)

Common questions about Ketrax (FAQ)

Q: Does Ketrax have uses beyond treating parasitic infections?

A: In addition to its primary role as a treatment for certain parasitic infections, levamisole was historically approved for use as an adjuvant therapy in combination with fluorouracil for specific stages of colon cancer after surgery. Official information also indicates its investigative use for its immunomodulatory properties in other conditions, such as nephrotic syndrome in children and the parasitic infection loiasis.

Q: Is Ketrax considered an immunomodulator?

A: Yes, regulatory documents classify Ketrax (levamisole) with a dual role: it is both an anthelmintic agent (targeting parasites) and an immunomodulator. This means that in addition to its anti-parasitic action, it has the ability to support the function of certain host defense cells, such as T-lymphocytes and phagocytes.

Q: Why is Ketrax sometimes used in combination with chemotherapy?

A: Ketrax was formerly used in combination with the chemotherapy agent fluorouracil (5-FU) as an adjuvant treatment following surgical resection for certain stages of colon cancer. This combination was studied as a means to potentially improve patient outcomes in that specific cancer treatment setting.

Q: Is it normal to feel dizzy or have stomach pain after taking Ketrax?

A: Official product information lists dizziness (a Nervous System Disorder) and stomach pain, or abdominal pain (a Gastrointestinal Disorder), among the commonly reported adverse reactions. These effects are recognized by regulatory authorities as possible occurrences when taking the medicine.

Q: Are there any reported long-term side effects of using Ketrax?

A: Serious adverse reactions are documented, and these are primarily associated with the repeated or long-term dosing used in historical adjuvant therapy regimens. These can include serious blood-related conditions like agranulocytosis (a severe reduction in white blood cells) and serious effects on the nervous system (neurotoxicity), notably leukoencephalopathy.

Q: Can Ketrax interact with common painkillers or antibiotics?

A: Official regulatory labels specifically warn of interactions with medicines like warfarin, phenytoin, and fluorouracil. However, official labels do not consistently list specific interactions with common over-the-counter painkillers or widely used classes of antibiotics, and caution is always advised.

Q: Can Ketrax interact with common herbal supplements?

A: Regulatory documents typically do not list specific interactions with herbal supplements. However, given the drug's known immunomodulatory action, considering supplements that affect immune function requires review with a healthcare provider.

Q: Is Ketrax safe for use in patients with a history of liver disease?

A: Ketrax is contraindicated (not recommended for use) in patients with pre-existing advanced liver disease. For patients with non-advanced liver impairment, the official prescribing information advises that the drug should be used with caution.

Q: Are there different brand names for the active ingredient in Ketrax?

A: Yes, the active ingredient in Ketrax, which is levamisole, is also marketed under other brand names, such as Ergamisol. The availability, approved forms, and specific uses of these brands vary widely by country and market.

Q: Is there research supporting the use of Ketrax as an immune booster?

A: Regulatory documents confirm its classification as an immunomodulator, noting it can support or restore depressed immune function in certain cells. This property is typically studied in the context of immune-mediated conditions rather than being marketed or used solely as a general 'immune booster.'

Q: Can Ketrax cause an allergic reaction?

A: Yes, the official prescribing information includes a known hypersensitivity to levamisole as an absolute contraindication. This indicates the potential for severe allergic reactions, and the medicine must not be used by individuals with a history of such a reaction.

Q: Is it true that Ketrax can cause a reaction if taken with certain foods?

A: Administration instructions state that the medicine can be taken with or without food, or preferably after a light meal. Regulatory documents do not specifically list particular foods that are prohibited due to an interaction.

Q: Does Ketrax affect the central nervous system?

A: Yes, official documents list common Nervous System Disorders like headache and dizziness as possible side effects. More severely, serious effects on the nervous system (neurotoxicity), including conditions like leukoencephalopathy, have been documented, particularly with prolonged, high-dose use.

Q: Has Ketrax been studied for other types of cancer besides colon cancer?

A: Clinical trials have also investigated levamisole's potential role in other cancers, including advanced breast cancer and lung cancer. However, official documentation generally notes that the evidence from these studies was inconclusive regarding its use in these other settings.

Q: Why is Ketrax sometimes compared to drugs like Ivermectin?

A: Ketrax (levamisole) is an anthelmintic agent, as is Ivermectin. Regulatory pharmacological data notes that co-administration of the two drugs can increase the bioavailability and systemic exposure of Ivermectin. This pharmacological interaction is often the basis for comparison.

Q: How does Ketrax affect the immune system?

A: It functions as a non-specific immunomodulator by supporting the activity of certain host defense cells, including T-lymphocytes and phagocytes (such as macrophages and neutrophils). It is designed to restore or enhance depressed host immune responses.

Q: Do different geographical regions use Ketrax for different primary purposes?

A: Yes, while the drug has been withdrawn from some Western markets due to safety concerns primarily related to long-term use, it remains on the WHO Essential Medicines List. Consequently, it is still used in many regions as a primary treatment for parasitic infections where it is effective and accessible.

Q: Is a prescription required to obtain Ketrax?

A: Yes, based on its classification and potential serious side effects, levamisole is categorized as a prescription-only medicine for human use. It must be obtained through a valid prescription from a licensed healthcare provider.

Q: What happens if Ketrax is exposed to light or moisture?

A: Official storage instructions require the medicine to be stored in a dry place and to be protected from direct sunlight. Exposure to light or moisture can potentially compromise the product's stability and lead to a loss of its intended potency.

Q: Does Ketrax interact with any medications for diabetes or blood pressure?

A: Specific interactions with common medications for diabetes or high blood pressure are not consistently documented across major regulatory labels. However, as with all medications, it is important to disclose all concurrent treatments to a healthcare professional.

Q: Can Ketrax cause problems with fertility or affect the reproductive system?

A: Regulatory information advises that the drug may have harmful effects on the unborn child, and a need for effective birth control during treatment is noted in prescribing information. It is also not recommended during pregnancy or breastfeeding unless deemed essential by a physician, due to insufficient data on potential risks.

Q: What makes Ketrax effective against specific types of nematodes?

A: The drug is effective against susceptible nematodes (roundworms) because its anthelmintic action involves acting on the worm's neuromuscular system. It specifically activates the nicotinic acetylcholine receptors in the parasite, which causes spastic paralysis and expulsion of the worm.

Q: How long after treatment can one expect parasite eggs to be cleared from the stool?

A: The drug works by paralyzing and expelling the live adult worms, often within 24 hours of administration. However, levamisole is not ovicidal (it does not kill the eggs), so the full clearance time for all eggs to be expelled is variable and depends on the body's natural processes.

How should Ketrax be stored and disposed of?

Ketrax (levamisole) must be stored in a cool, dry, and well-ventilated place and must be protected from direct sunlight. The product should be kept away from heat and sources of ignition and should not be stored with strong oxidizing agents. The container must be kept tightly closed and in a properly labeled condition.

For security, the medicine is required to be stored locked up (Precautionary Statement P405) and out of the reach of children.

Disposal of unused or expired product must be conducted to an approved waste disposal plant (Disposal code P501), according to local, regional, and national regulations. The product should not be kept if it is outdated.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

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