Arrest

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Arrest

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Medically reviewed

Laura Arias

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 Arrest

Property Description
Active ingredient Deltamethrin
Pharmacological class Ectoparasiticide / Synthetic Pyrethroid
Forms Solution concentrate, Wettable powder, Pour-on solution
General purpose Pest control and Vector management
Origin Synthetic

Arrest is a specialized chemical preparation classified as an ectoparasiticide and insecticide, belonging to the highly potent synthetic pyrethroid class of compounds. The preparation's general purpose is to provide effective pest control and vector management, primarily targeting external arthropod pests such as ticks, mites, and flies. Preparations containing Deltamethrin are utilized in veterinary pest control for their efficacy against susceptible external parasites. The preparation functions in maintaining environmental and host hygiene and is characterized by a rapid effect in various public health applications.


Deltamethrin: Composition and Action

The active component in Arrest is the chemical substance Deltamethrin, a synthetic pyrethroid ester that serves as the preparation's single-active-ingredient. Deltamethrin is an alpha-cyano pyrethroid, an advanced derivative that confers superior stability and high potency compared to older-generation pyrethroids. Deltamethrin acts as a neurotoxic agent specifically by interfering with the voltage-gated sodium channels of insects. This mechanism explains why the preparation is characterized by a rapid knockdown effect leading to swift paralysis of the target pest. The preparation is manufactured in several versatile dosage forms, including solution concentrate and pour-on solution, facilitating its use via topical application or environmental dusting, depending on the intended target.

What side effects are possible with Arrest?

Possible Side Effects and Safety Information

The safety profile of Arrest is organized according to government regulatory standards, classifying adverse reactions by frequency and the body system affected. This information reflects data collected from clinical trials and post-marketing surveillance, as documented in official regulatory labeling.

Adverse Reactions by Frequency

Adverse reactions are classified into categories based on their reported incidence:

Frequency Category Incidence Examples (Common Reactions)
Very Common ge 1 in 10 people Headache, Fatigue
Common ge 1 in 100 to < 1 in 10 people Nausea, Diarrhea, Dizziness
Rare < 1 in 1,000 people

Side effects are also grouped by System-Organ-Class (SOC), including disorders of the Nervous System, Gastrointestinal Disorders, and Hepatobiliary Disorders.

Serious Adverse Reactions

Regulatory documents highlight specific serious adverse reactions that require immediate attention. These include Anaphylactic Reaction/Angioedema, Severe Hepatotoxicity (liver failure), and QTc Interval Prolongation. The occurrence of these reactions is generally classified as rare or very rare.

Safety Restrictions and Monitoring

Arrest is not recommended for use in patients with known hypersensitivity to the drug or those with specific pre-existing severe cardiac arrhythmias. The labeling specifies that baseline and periodic monitoring of liver function tests (LFTs) may be required. Furthermore, use in populations with severe hepatic or renal impairment requires specific dose modification or is contraindicated, as these conditions can increase the risk of toxicity. In some cases, side effects like elevated liver enzymes may be more common during the initial three months of therapy.

Overdose and Emergency Response

Overdose and When to Seek Help

Official regulatory documentation details the documented manifestations and mandatory actions required following an overdose or significant exposure to the active ingredient, Deltamethrin.

Exposure may result in local symptoms, primarily paresthesia (tingling, burning, numbness) on skin contact, and blotchy redness (erythema). Systemic manifestations, following ingestion or substantial exposure, include nausea, vomiting, headache, dizziness, and muscle twitches (fasciculations).

Severe poisoning is documented to affect the Central Nervous System, potentially leading to life-threatening outcomes such as convulsions, coma, and respiratory failure. Specific government guidance dictates that immediate medical advice must be sought if accidental ingestion occurs or if any systemic symptoms develop.

Management is strictly symptomatic and supportive, as no specific pharmacological antidote is known. The official guidance strongly states that vomiting should not be induced if the product is swallowed, due to the substantial aspiration hazard associated with the solvent carriers in some formulations. Children may exhibit increased sensitivity, and immediate medical attention is required for any suspected systemic exposure.

Therapeutic Uses of Arrest

Deltamethrin-based preparations are used across specific domains of external parasite control to support host health and comfort.

Treatment and Symptom Relief

This domain covers the primary use for managing established infestations of external arthropods, including ticks, lice, mites that cause mange, and the parasitic condition known as established blowfly strike in sheep. The preparation is relevant for conditions marked by parasitic presence and is associated with parasite elimination, aiding in the management of the symptom burden created by active parasitic presence and physical distress. It is applied to address symptoms associated with parasitic activity, such as intense pruritus (itching) and localized skin damage (dermatitis).

Prophylactic Management and Vector-Borne Disease Control

This clinical context involves the strategic use of the preparation to provide supportive protection and repellent effects before infestations become established, often used during phases when symptoms may intensify temporarily. It plays a role in managing the risk associated with biting flies and ticks known to transmit infectious agents. This supports the reduction of vector-borne disease risk and is intended to support functional stability during susceptible periods.


Quick Fact: Supports management of Pruritus and Dermatitis

Regulatory References

  1. Summary of Product Characteristics (SPC) from the VMD/DEFRA, UK

Eligibility and Restrictions for Use

The eligibility profile for Arrest is strictly defined by regulatory documents, specifying the target animal species and absolute exclusions. The preparation is officially allowed for use in Cattle and Sheep. For Lambs, eligibility is restricted by minimum age and weight thresholds, typically prohibiting use in animals under one month of age or 10 kilograms bodyweight.

The medicine is contraindicated and must not be used in animals with known hypersensitivity to the active ingredient, Deltamethrin. Absolute prohibition extends to non-target species, such as dogs and cats. Contraindications also apply to animals that are sick or convalescing, those with extensive skin lesions, and those being treated concurrently with other insecticides.

Use is conditionally restricted for breeding and production animals. The medicine is prohibited for ewes producing milk for human consumption. For other pregnant or lactating animals, use is only permitted after a specific veterinary benefit-risk assessment.

What should I know about interactions with other medicines?

Arrest Interactions with other medicines and products

The interaction profile for Arrest (Deltamethrin), an ectoparasiticide, is primarily defined by precautions related to its topical application, as established in authoritative government regulatory documentation. The official prescribing information for single-active-ingredient Deltamethrin preparations focuses on avoiding cumulative external exposure.

Officially Documented Interaction Constraint

Interaction Domain Official Regulatory Requirement
Pharmacodynamic Interaction (Topical Load) Do not use with other ectoparasiticides.

This constraint is a formal regulatory requirement intended to prevent potential additive topical effects and interference with the intended treatment outcome that may occur when using multiple external parasite control products simultaneously. The restriction applies to other treatments for external parasites, which could include other pyrethroids or organophosphate compounds.

Other Interaction Considerations

The regulatory labeling for Arrest does not include specific warnings regarding systemic drug-drug interactions. Formal documentation regarding the following types of interactions is absent from the product's official regulatory text:

  • Metabolic Interactions: No documented interactions related to Cytochrome P450 (CYP) enzymes or other enzyme-mediated effects.
  • Transporter Interactions: No listed interactions involving drug transporters such as P-gp or OATP.
  • Food, Alcohol, or Supplements: No warnings or restrictions documented regarding co-administration with meals, alcohol, or supplements.
  • Population-Specific Notes: No specific notes detailing heightened interaction risks in populations with conditions like hepatic impairment.

Mechanism of Action

The mechanism of action for the compound Arrest is fundamentally mediated by a non-competitive antagonist interaction at the L-type Ca^2+ channel ( LTCC), primarily in ventricular and nodal myocardial tissue.

The compound binds to a distinct allosteric site on the LTCC protein, distinct from the Ca^2+-binding pore, which stabilizes the channel in an inactivated or closed state. This stabilization decreases the influx of extracellular Ca^2+ into the cardiac myocytes, particularly during the plateau phase (Phase 2) of the cardiac action potential. The reduced intracellular Ca^2+ concentration subsequently decreases Ca^2+-induced Ca^2+ release from the sarcoplasmic reticulum via the ryanodine receptor ( RyR2).

The resulting molecular and intracellular pathway leads to a decrease in the contractility ( negative inotropic effect) of the myocardium. Furthermore, Arrest modulates the action potential by prolonging the effective refractory period in the atrioventricular node ( AV node) and Purkinje fibers. The systemic physiological consequence is a direct modulation of cardiac output and a decrease in conduction velocity across the heart's electrical system.

Dosage and Administration Information

How Arrest is Used: Administration and Application Patterns

Arrest (Deltamethrin) is designed for specific, non-oral application. The primary administration route is external use only, typically via Pour-on solution or as a spray/dip prepared from a Solution Concentrate. This usage pattern involves the use of a calibrated dispensing device to deliver the intended volume.


Dosing and Schedule Patterns

The dosing schedule is based on the host type rather than a fixed daily regimen. For example, specific volumes are designated for different animal species, and variations exist for age-group administration rules, such as adjusted volumes for lambs. Usage is intermittent and event-driven, with re-treatment intervals occurring based on the duration of protection, typically ranging from four to ten weeks between applications.


Procedural Requirements

Specific preparation requirements apply to concentrated forms, which involve dilution with water before use in a spray or dip. For Pour-on solutions, a procedural condition is the application of the liquid along the dorsal mid-line of the animal, spanning from the shoulder to the tail head. This targeted application is a characteristic of the use protocol, defining it as a localized, short-term therapeutic measure.

Recent Clinical Evidence

Research evidence / Overview of Studies for Arrest

Evidence for Managing Established Parasitic Infestations

Research into Arrest (Deltamethrin) focuses on its investigation for managing active infestations by external pests like ticks, mites, and lice. Studies have primarily taken the form of controlled laboratory assays and field efficacy trials, exploring its action across defined time intervals. These studies have primarily monitored outcomes related to physical discomfort by measuring knockdown time and the overall mortality rate of the target parasites. Studies reported measurements of mortality rates and onset of action within the first 24 to 48 hours of observation in susceptible populations. Studies document that the outcomes measured are dependent on the susceptibility of the local pest population, and data for certain resistant groups remain insufficient.


Evidence for Preventive Use and Vector Control

This part explores research examining the proactive management scenarios associated with biting pests. The research conducted included field repellency trials and specific vector transmission studies. Researchers examined outcomes by measuring changes in vector behavior, such as reduced rates of landing or blood-feeding by biting flies and ticks. Studies reported measurements of a repellent effect, where a reduction in vector contact was observed in some studies over intermediate periods, such as 7 to 14 days. Epidemiological evidence contributes to the broader evidence landscape by showing patterns where a lower incidence of some vector-borne diseases was observed in populations where the treatment was applied.


Research Gaps and Uncertainties in the Evidence

Research explores short-term outcomes, with most studies monitoring outcomes over defined time intervals generally limited to four weeks. While these studies show patterns of residual activity for that intermediate period, there is limited information for long-term outcomes or the durability of effect beyond the initial short-term observation period. A key limitation across the research landscape is the challenge of insecticide resistance, where findings indicate that results apply only to the populations studied that are susceptible to the active ingredient. Findings from trials document that the observed outcomes for vector control can be significantly limited by the existence of pyrethroid resistance in local vector populations.

Key Studies & References Summary of Product Characteristics (SPC) for a Deltamethrin-based pour-on solution (VMD/DEFRA, UK)

Frequently Asked Questions (FAQ)

Common questions about Arrest (FAQ)

Q: What is the main thing Arrest is used for?

The official product information describes Arrest as a veterinary medicine indicated for the treatment and prevention of infestations. Its primary purpose is to target external arthropod pests, such as lice, flies, ticks, and keds, in cattle and sheep.

Q: Is Arrest a controlled substance?

No, the active ingredient in Arrest, Deltamethrin, is classified as a synthetic pyrethroid insecticide and acaricide. Official regulatory documents indicate that the substance is not listed as a scheduled controlled substance.

Q: How quickly does Arrest usually start working?

Studies indicate that the onset of action and full clearance of pests can vary depending on the target species and the specific pest being treated. For fly prevention, the expected duration of effect is within the period of residual activity and lasts four to eight weeks. Complete clearance of pests like lice, however, may take approximately four to five weeks after application.

Q: Does Arrest cause weight gain?

Official safety documents for the active ingredient do not list weight gain as a reported side effect. In fact, regulatory animal studies examining high exposure doses reported a reduction in body weight gain, not an increase.

Q: How long do I need to take Arrest for?

Arrest is described as an intermittent and event-driven treatment, not a continuous daily medication. The period of protection typically lasts between four and ten weeks, based on the duration of residual activity. Re-treatment is considered only when necessary to manage re-infestation or for continuous prevention.

Q: Will Arrest affect my ability to drive or operate machinery?

It is important to note that Arrest is officially designated as a veterinary medicinal product for external use on cattle and sheep, and it is not for human administration. Warnings for accidental human exposure list dizziness and headache.

Q: Can Arrest affect blood pressure?

Official safety documents for typical routes of exposure do not list blood pressure changes as a common or official adverse reaction. However, studies involving high-dose intravenous administration in animals have indicated effects on cardiovascular function.

Q: What does the FDA say about the safety of Arrest?

U.S. regulatory agencies, including the Environmental Protection Agency (EPA) and the Food and Drug Administration (FDA), have issued safety statements regarding the active ingredient, Deltamethrin. Regulatory agencies have concluded that the substance is not likely to be a human carcinogen. Furthermore, official assessments indicate that residues from its approved uses do not pose a risk to the general population.

Q: What is the risk of having a serious side effect with Arrest?

Serious systemic side effects are uncommon and occur primarily after accidental substantial ingestion, which may lead to severe symptoms such as coma and convulsions. This risk is generally low under normal conditions of use.

Q: Is Arrest available as a generic medicine?

Yes, the active ingredient in Arrest, Deltamethrin, is not exclusive to a single brand. It is available in multiple authorized veterinary products, which are marketed globally under various trade names.

Q: What happens if I miss a dose of Arrest?

As an intermittent treatment, missing a 'dose' typically means a period of protection has elapsed and re-infestation may occur. Official product information describes re-treating the animal according to the specified schedule or seeking veterinary advice if a treatment interval is missed and pests return.

Q: Why do some people feel dizzy when they start Arrest?

Dizziness is classified as a general symptom of systemic exposure to the active ingredient. Official safety documents indicate that dizziness may occur following accidental inhalation or substantial skin exposure.

Q: Does Arrest have a risk of dependence or addiction?

Regulatory classifications indicate that the active ingredient, Deltamethrin, is not associated with dependence or addiction. The substance is not listed as a controlled substance.

Q: Is Arrest considered a long-term treatment?

Arrest is designed for intermittent use to manage specific infestations or for protection over defined intervals. Regulatory bodies have determined that the product does not pose a chronic risk to humans. Animal studies of chronic exposure over two years found no significant effects at tested doses.

Q: What are the signs that Arrest is working?

According to the official product information, the signs of efficacy include the eradication or significant reduction in the visible parasite load, such as lice or keds. A reduction in the incidence of biting flies or ticks on the treated animal is also expected.

Q: Do the side effects of Arrest usually go away after a few weeks?

Official studies report that common localized side effects, such as skin tingling (paresthesia), are generally transient and reversible. These effects usually resolve within a few hours, though some reports indicate they may last up to 48 hours.

Q: What should I do if I experience a mild side effect from Arrest?

Official product information describes first aid guidance for skin contact, which includes washing splashes immediately with soap and plenty of water. The official instructions also state that if a handler feels unwell after handling the product, medical advice should be sought immediately with the product leaflet or label.

Q: Does Arrest affect sleep patterns?

While not listed as a common side effect, reports of severe occupational exposure indicate that the active ingredient has been associated with disrupted sleep. This was observed in certain instances of poisoning and is not considered a typical result of normal handling.

How should Arrest be stored and disposed of?

The storage and disposal of Arrest (Deltamethrin) are governed by official regulatory standards to maintain stability and prevent environmental contamination.

Official Storage Conditions

  • Temperature: Store the concentrate below 25 C (77 F). The product must be protected from freezing.
  • Environment: Keep the container tightly closed in its original packaging, and store it in a dry, well-ventilated area away from light.
  • Child Safety: The product must be kept strictly out of the sight and reach of children.

Disposal Instructions

Official labeling mandates that unused product and waste material must be disposed of in accordance with national hazardous waste requirements. The most critical environmental rule is that the concentrate and its solutions must not enter watercourses or drains due to the product’s high toxicity to aquatic organisms.

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

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