Clinical data | |
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Trade names | Albenza, Eskazole, Valbazen, Zentel, others |
AHFS/Drugs.com | Monograph |
MedlinePlus | a610019 |
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Routes of administration | By mouth |
ATC code | |
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Pharmacokinetic data | |
Bioavailability | <5% [2] |
Protein binding | 70% [2] |
Metabolism | Hepatic [2] |
Elimination half-life | 8-12 hours [2] |
Excretion | Bile (humans) Urine (ruminants) |
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ChEBI | |
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NIAID ChemDB | |
CompTox Dashboard (EPA) | |
ECHA InfoCard | 100.053.995 |
Chemical and physical data | |
Formula | C12H15N3O2S |
Molar mass | 265.33 g·mol−1 |
3D model (JSmol) | |
Melting point | 208 to 210 °C (406 to 410 °F) |
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Albendazole is a broad-spectrum antihelmintic and antiprotozoal agent of the benzimidazole type. [3] It is used for the treatment of a variety of intestinal parasite infections, including ascariasis, pinworm infection, hookworm infection, trichuriasis, strongyloidiasis, taeniasis, clonorchiasis, opisthorchiasis, cutaneous larva migrans, giardiasis, and gnathostomiasis, among other diseases. [3]
Common side effects include nausea, abdominal pain, and headache. [3] Rare but potentially serious side effects include bone marrow suppression which usually improves on discontinuing the medication. Liver inflammation has been reported and those with prior liver problems are at greater risk. [3] It is pregnancy category D in Australia, meaning it may cause harm if taken by pregnant women. [3] [4]
Albendazole was developed in 1975. [5] It is on the World Health Organization's List of Essential Medicines. [6]
Albendazole is an effective treatment for:
Though albendazole is effective in treating many diseases, it is only FDA-approved for treating hydatid disease caused by dog tapeworm larvae and neurocysticercosis caused by pork tapeworm larvae. [25]
Albendazole is a pregnancy class D drug in Australia. It is contraindicated in the first trimester of pregnancy, and should be avoided up to one month before conception. While studies in pregnant rats and rabbits have shown albendazole to be teratogenic, [26] [27] albendazole has been found to be safe in humans during the second and third trimesters. [28] [29] It can, however, possibly cause infantile eczema when given during pregnancy. [30]
In pregnant dogs, albendazole use has led to puppies with reduced weight and with cleft palates. Birds have lower rates of laying eggs and hatching when given albendazole. [31]
Albendazole sulfoxide is secreted into breast milk at around 1.5% of the maternal dose, though oral absorption is poor enough that it is unlikely to affect nursing infants. [26] [32]
Hypersensitivity to the benzimidazole class of compounds contraindicates its use. [18]
The most common side effects of albendazole are experienced by over 10% of people and include headache and abnormal liver function. [2] Elevation of liver enzymes occurs in 16% of patients receiving treatment specifically for hydatid disease and goes away when treatment ends. [12] [33] Liver enzymes usually increase to two to four times the normal levels (a mild to moderate increase). [34] An estimated 1–10% of people experience abdominal pain, nausea or vomiting, dizziness or vertigo, increased intracranial pressure, meningeal signs, temporary hair loss, and fever. The headache, nausea, and vomiting are thought to be caused by the sudden destruction of cysticerci (tapeworm larvae), which causes acute inflammation. [35] Fewer than 1% of people get hypersensitivity reactions such as rashes and hives, leukopenias (drop in white blood cell levels) such as agranulocytosis and granulocytopenia, thrombocytopenia (reduced platelet count), pancytopenia (drop in white blood cells, red blood cells, and platelets), hepatitis, acute liver failure, acute kidney injury, irreversible bone marrow suppression, and aplastic anemia. [2] [36]
Side effects can be different when treating for hydatid disease versus neurocysticercosis: for example, those being treated for the former are more likely to experience elevated liver enzymes and abdominal pain, while those being treated for the latter are more likely to experience headache. [33] Treating hydatid disease can also unmask undiagnosed neurocysticercosis. [33] People receiving albendazole for the treatment of neurocysticercosis can have neurological side effects such as seizures, increased intracranial pressure, and focal signs caused by the inflammatory reaction that occurs when parasites in the brain are killed. Steroids and anticonvulsants are often given with albendazole when treating neurocysticercosis to avoid these effects. [33] Those being treated for retinal neurocysticercosis can face retinal damage if they are not first checked for ocular cysticeri, since changes to existing lesions in the eye by albendazole can cause permanent blindness. [12]
Because of its low solubility, albendazole often cannot be absorbed in high enough quantities to be toxic. [35] The oral LD50 of albendazole in rats was found to be 2,500 mg/kg. [27] It takes 20 times the normal dose to kill a sheep, and 30 times the normal dose to kill cattle. [1] Overdose affects the liver, testicles, and GI tract the most. It can manifest with lethargy, loss of appetite, vomiting, diarrhea, intestinal cramps, dizziness, convulsions, and sleepiness. There is no specified antidote. [31]
The antiepileptics carbamazepine, phenytoin, and phenobarbital lower the plasma concentration and half-life of albendazole sulfoxide's R(+) enantiomer. [37]
Drug | Change in AUC | Change in Cmax |
---|---|---|
Carbamazepine | 49% decrease | 50–63% decrease |
Phenobarbitol | 61% decrease | 50–63% decrease |
Phenytoin | 66% decrease | 50–63% decrease |
The antacid cimetidine heightens serum albendazole concentrations, increases the half-life of albendazole, and doubles albendazole sulfoxide levels in bile. [38] [33] It was originally thought to work by increasing albendazole bioavailability directly; however, it is now known that cimetidine inhibits the breakdown of albendazole sulfoxide by interfering with CYP3A4. [15] The half-life of albendazole sulfoxide thus increases from 7.4 hours to 19 hours. [39] This might be a helpful interaction on more severe cases, because it boosts the potency of albendazole. [40] Paradoxically, cimetidine also inhibits the absorption of albendazole by reducing gastric acidity. [39]
Several other interactions exist. Corticosteroids increase the steady-state plasma concentration of albendazole sulfoxide; [12] dexamethasone, for example, can increase the concentration by 56% by inhibiting the elimination of albendazole sulfoxide. [33] [35] The anti-parasitic praziquantel increases the maximum plasma concentration of albendazole sulfoxide by 50%, [33] and the anti-parasitic levamisole increases the AUC (total drug exposure) by 75%. [22] Grapefruit inhibits the metabolism of albendazole within the intestinal mucosa. Finally, long-term administration of the antiretroviral ritonavir, which works as a CYP3A4 inhibitor, decreases the maximum concentration of albendazole in the plasma as well as the AUC. [39]
This section may require cleanup to meet Wikipedia's quality standards. The specific problem is: should be sorted by target molecule, specifically into tubulin-related (intestines, spindle, shape) and unrelated parts.(January 2021) |
As a vermicide, albendazole causes degenerative alterations in the intestinal cells of the worm by binding to the colchicine-sensitive site of β-tubulin, thus inhibiting its polymerization or assembly into microtubules (it binds much better to the β-tubulin of parasites than that of mammals). [3] [33] Albendazole leads to impaired uptake of glucose by the larval and adult stages of the susceptible parasites, and depletes their glycogen stores. Albendazole also prevents the formation of spindle fibers needed for cell division, which in turn blocks egg production and development; existing eggs are prevented from hatching. [15] [41] Cell motility, maintenance of cell shape, and intracellular transport are also disrupted. [42] At higher concentrations, it disrupts the helminths' metabolic pathways by inhibiting metabolic enzymes such as malate dehydrogenase and fumarate reductase, with inhibition of the latter leading to less energy produced by the Krebs cycle. [1] [31] [43] Due to diminished ATP production, the parasite is immobilized and eventually dies.
Some parasites have evolved some resistance to albendazole by having a different set of acids constituting β-tubulin, decreasing the binding affinity of albendazole. [33] Some parasites (especially filarial nematodes) live in symbiosis with Wolbachia , a type of intracellular parasite bacteria. In such cases the Wolbachia are necessary to the survival of the parasitic worms. [44] Elimination of Wolbachia from these filarial nematodes generally results in either death or sterility of the host nematode. [45]
Oral absorption of albendazole varies among species, with 1–5% of the drug being successfully absorbed in humans, 20–30% in rats, and 50% in cattle. [46]
The absorption also largely depends on gastric pH. People have varying gastric pHs on empty stomachs, and thus absorption from one person to another can vary wildly when taken without food. [21] Generally, the absorption in the GI tract is poor due to albendazole's low solubility in water. [3] It is, however, better absorbed than other benzimidazole carbamates. [22] Food stimulates gastric acid secretion, lowering the pH and making albendazole more soluble and thus more easily absorbed. [39] Oral absorption is especially increased with a fatty meal, as albendazole dissolves better in lipids, allowing it to cross the lipid barrier created by the mucus surface of the GI tract. [42] [46] To target intestinal parasites, albendazole is taken on an empty stomach to stay within the gut. [47]
Absorption is also affected by how much of the albendazole is degraded within the small intestine by metabolic enzymes in the villi. [21]
The pharmacokinetics of albendazole differ slightly between men and women: women have a lower oral clearance and volume of distribution, while men have a lower serum peak concentration. [39]
Albendazole undergoes very fast first-pass metabolism in all species, such that the unchanged drug is undetectable in plasma. [46] Most of it is oxidized into albendazole sulfoxide (also known as ricobendazole and albendazole oxide [27] [48] ) in the liver by cytochrome P450 oxidases (CYPs) and a flavin-containing monooxygenase (FMO), [49] which was discovered later. [50] In humans, the cytochrome P450 oxidases are thought to include CYP3A4 [51] and CYP1A1, [46] while those in the rats are thought to be CYP2C6 and CYP2A1. [52]
Oxidation to albendazole sulfoxide by FMO produces R(+) enantiomers, while oxidation the cytochromes and by some enzymes in the gut epithelium produce S(-). Different species produce the R(+) and S(-) enantiomers in different quantities; humans, dogs, and most other species [52] produce the R(+) enantiomer more (with the human AUC ratio being 80:20). [35] [39] [46] Compared to the S(-) enantiomer, the R(+) has greater pharmacological activity, lasts longer in the bloodstream, is found in higher concentrations in the infected host tissues, and is found in higher concentrations within the parasites themselves. [52] [42] Some albendazole is also converted to hydroxyalbendazole, mainly by CYP2J2. [30] [53]
For systemic parasites, albendazole acts as a prodrug, while albendazole sulfoxide reaches systemic circulation and acts as the real antihelminthic. [15] Albendazole sulfoxide is able to cross the blood–brain barrier and enter the cerebrospinal fluid at 43% of plasma concentrations; its ability to enter the central nervous system allows it to treat neurocysticercosis. [39]
Albendazole sulfoxide is converted to the inactive albendazole sulfone by cytochrome P450 oxidases, thought to include CYP3A4 [39] or CYP2C. [15] Other inactive metabolites include: 2-aminosulfone, ω-hydroxysulfone, and β-hydroxysulfone. [49] [35] The major final metabolites that are excreted by humans are: [15]
There are also some minor hydroxylated sulfated or glucuronidated derivatives. [15] No unchanged albendazole is excreted, as it is metabolized too quickly. [2]
In humans, the metabolites are excreted mostly in bile, with only a small amount being excreted in urine (less than 1%) and feces. [2] [15] In ruminants, 60–70% of the metabolites are excreted in urine. [31]
Like all benzimidazoles, albendazole has no residual effect, and thus protects poorly against reinfestations. [27]
Albendazole, patented in 1975, was invented by Robert J. Gyurik and Vassilios J. Theodorides and assigned to SmithKline Corporation. [54] [55] It was introduced in 1977 as an antihelminthic for sheep in Australia, and was registered for human use in 1982. [12] [15]
Brand names include: Albenza, [33] Alworm, Andazol, Eskazole, Noworm, Zentel, Alben-G, ABZ, Cidazole, Wormnil etc.
The pharmaceutical company Amedra increased the price after purchasing the rights to the drug, instead of lowering it as generics are predicted to do, drawing criticism from patients' rights advocates. [56]
In 2013, GlaxoSmithKline donated 763 million albendazole tablets for the treatment and prevention of parasitic infections in developing countries, bringing the total to over 4 billion tablets donated since 1998. [57]
Albendazole and related compounds or metabolites like albendazole sulfone (ALB-SO2) exhibit antibacterial effects via an unknown, possibly FtsZ-related, mechanism. It inhibits division of Wolbachia and Mycobacterium tuberculosis , turning them into a long "filament" shape as they grow and fail to divide. Since Brugia malayi relies on symbiotic Wolbachia, this would mean that albendazole is targeting both the worm and its essential symbioant. [58]
Albendazole is mainly used in cattle and sheep, but has found some use in cats and dogs as well; [28] it is also used in ratite birds for flagellate parasites and tapeworms. It is also used off-label to treat endoparasites in goats and pigs. [1]
Cattle | Sheep | Others | |
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Platyhelminthes (flatworms) | |||
Trematodes | |||
Dicrocoelium (liver flukes) | D. dendriticum (lancet liver fluke) [62] | D. dendriticum [63] | |
Fasciola (liver flukes) | F. hepatica | F. hepatica | For F. hepatica and F. gigantica in people [3] |
Fascioloides (liver flukes) | F. magna [62] | F. magna | Also for F. magna in South American camelids (ex. llama and alpaca) [63] |
Paragonimus (lung flukes) | — | — | For P. kellicotti in cats and dogs [63] |
Platynosomum | — | — | For Platynosomum infections in cats |
Opisthorchiidae | — | — | For Opisthorchiidae infections in cats |
Cestodes (tapeworms) | |||
Echinococcus | – | — | For Echinococcus cysts in horses and humans [63] [3] |
Moniezia | M. expansa M. benedini | M. expansa | |
Taenia | T. saginata larvae | — | For T. saginata, T. solium , and T. crassiceps in humans [9] [10] and Taenia infections in dogs [64] |
Thysanosoma | — | T. actinoides | |
Nematodes (roundworms) | |||
Ancylostoma | — | – | For Ancylostoma infections in dogs, cats, and humans [63] [3] |
Bunostomum | B. phlebotomum | – | |
Capillaria | — | — | For causative agents of various forms of capillariasis in cats and dogs (including C. philippinensis , C. hepatica , C. aerophila , and C. plica ) and intestinal capillariasis (C. philippinensis) in humans. |
Chabertia | — | C. ovina | |
Cooperia | C. oncophora C. punctata | C. oncophora | |
Dictyocaulus (lungworm) | D. viviparus | D. filaria | For D. amfieldi infections in horses |
Filaroides (lungworm) | — | — | For F. hirthi and F. osleri in dogs |
Haemonchus | H. contortus H. placei | H. contortus | |
Marshallagia | — | M. marshalli | |
Metastrongylus | — | — | For M. apri in swine |
Nematodirus | N. spathiger N. helvetianus | N. spathiger N. filicollis | |
Parascaris | — | — | For P. equorum in horses [60] |
Ostertagia | O. ostertagi | O. circumcincta | For O. bifurcum in humans |
Oesophagostomum | O. radiatum | O. columbianum | |
Strongyloides | — | — | For S. stercoralis in dogs and humans [3] [63] |
Strongylus | — | — | For S. equinus in horses [63] |
Toxocara | — | — | For T. canis infections in dogs [63] and toxocariasis in humans (caused by T. canis and T. cati ) |
Trichostrongylus | T. axei T. colubriformis | T. axei T. colubriformis | For any Trichostrongylus infection in humans |
Trichuris (whipworm) | Most species, but those usually found in cattle are: [65] T. discolor T. globulosa T. ovis | Most species, but those usually found in sheep are: [65] T. discolor T. globulosa T. ovis | Albendazole is also used for Trichuris infections in humans (usually T. trichiura , causative agent of trichuriasis), dogs (usually T. vulpis and T. campanula), cats (usually T. serrata and T. campanula), pigs (usually T. suis ), and other ruminants (same species as those found in cattle and sheep). [65] |
Other | |||
Encephalitozoon | — | — | For E. cuniculi infections (microsporidiosis) in humans and rabbits |
Giardia | G. lamblia (causative agent of giardiasis) | — | Also treats giardiasis in humans, dogs, and small mammals |
Leishmania | — | — | Treats leishmaniasis, caused by various species of Leishmania, in dogs |
Albendazole has been used as an antihelminthic and for control of flukes in a variety of animal species, including cattle, sheep, goats, swine, camels, dogs, cats, elephants, poultry, and others. [31] [66] Side effects include anorexia in dogs and lethargy, depression, and anorexia in cats, [1] with more than 10% of dogs and cats having anorexia. [32] Of dogs and cats, 1–10% experience elevated liver enzymes, nausea, vomiting, and diarrhea. Less than 1% experience neutropenia or aplastic anemia, though these require a use of at least 5 days. [32] While it is also associated with bone marrow suppression and toxicity in cats and dogs at high doses, albendazole has a higher margin of safety in other species. [28] [59] Thus, it is usually only prescribed in cats and dogs when an infection is present that is resistant to the commonly prescribed metronidazole and fenbendazole. [67]
It is extensively used for ruminant livestock in Latin America. [27] It is marketed for this purpose by Zoetis (formerly Pfizer Animal Health) in numerous countries (including the United States and Canada) as Valbazen in oral suspension and paste formulations; [1] [28] by Interchemie in the Netherlands and elsewhere as Albenol-100; by Channelle Animal Health Ltd. in the United Kingdom as Albex; and by Ravensdown in New Zealand (as Albendazole). Although most formulations are administered orally, Ricomax (ricobendazole, or albendazole sulfoxide) is administered by subcutaneous injection.[ citation needed ]
Albendazole has greater bioavailability in ruminants: some albendazole sulfoxide, when released back into the rumen, is reduced to albendazole by the resident microbiota, with a preference of the (+) enantiomer being the substrate. [52] [42] Cats and dogs, having no rumen reservoir, sometimes need higher or more frequent doses as compared to ruminants. In dogs, albendazole sulfoxide is detectable in the plasma for less than 12 hours, but in sheep and goats, it remains at measurable levels for around three days. [31]
This section needs additional citations for verification .(August 2017) |
The limitations in early pregnancy are due to a limited period during which teratogenic effects may occur. Summarized research data relating to the durations of these preslaughter and early pregnancy periods when albendazole should not be administered are found in US FDA NADA 110-048 (cattle) and 140-934 (sheep). Some data and inferences regarding goats are found in US FDA Supplemental NADA 110-048 (approved January 24, 2008).
Maximum residue limits (MRLs) for albendazole in food, adopted by the FAO/WHO Codex Alimentarius in 1993, are 5000, 5000, 100, and 100 micrograms per kilogram of body weight (μg/kg) for kidney, liver, fat, and muscle, respectively, and 100 μg/L for milk. For analysis purposes, MRLs of various nations may pertain to concentration of a marker substance which has been correlated with concentrations of the administered substance and its metabolized products. For example, in Canada, the marker substance specified by Health Canada is albendazole-2-aminosulfone, for which the MRL in liver of cattle is 200 μg/kg.
There is a 27-day cattle withdrawal time for meat. [28]
Echinococcosis is a parasitic disease caused by tapeworms of the Echinococcus type. The two main types of the disease are cystic echinococcosis and alveolar echinococcosis. Less common forms include polycystic echinococcosis and unicystic echinococcosis.
Filariasis is a parasitic disease caused by an infection with roundworms of the Filarioidea type. These are spread by blood-feeding insects such as black flies and mosquitoes. They belong to the group of diseases called helminthiases.
Praziquantel (PZQ), sold under the brandname Biltricide among others, is a medication used to treat a number of types of parasitic worm infections in mammals, birds, amphibians, reptiles, and fish. In humans specifically, it is used to treat schistosomiasis, clonorchiasis, opisthorchiasis, tapeworm infections, cysticercosis, echinococcosis, paragonimiasis, fasciolopsiasis, and fasciolosis. It should not be used for worm infections of the eye. It is taken by mouth.
Hymenolepiasis is infestation by one of two species of tapeworm: Hymenolepis nana or H. diminuta. Alternative names are dwarf tapeworm infection and rat tapeworm infection. The disease is a type of helminthiasis which is classified as a neglected tropical disease.
Fasciolosis is a parasitic worm infection caused by the common liver fluke Fasciola hepatica as well as by Fasciola gigantica. The disease is a plant-borne trematode zoonosis, and is classified as a neglected tropical disease (NTD). It affects humans, but its main host is ruminants such as cattle and sheep. The disease progresses through four distinct phases; an initial incubation phase of between a few days up to three months with little or no symptoms; an invasive or acute phase which may manifest with: fever, malaise, abdominal pain, gastrointestinal symptoms, urticaria, anemia, jaundice, and respiratory symptoms. The disease later progresses to a latent phase with less symptoms and ultimately into a chronic or obstructive phase months to years later. In the chronic state the disease causes inflammation of the bile ducts, gall bladder and may cause gall stones as well as fibrosis. While chronic inflammation is connected to increased cancer rates, it is unclear whether fasciolosis is associated with increased cancer risk.
Taenia solium, the pork tapeworm, belongs to the cyclophyllid cestode family Taeniidae. It is found throughout the world and is most common in countries where pork is eaten. It is a tapeworm that uses humans as its definitive host and pigs as the intermediate or secondary hosts. It is transmitted to pigs through human feces that contain the parasite eggs and contaminate their fodder. Pigs ingest the eggs, which develop into larvae, then into oncospheres, and ultimately into infective tapeworm cysts, called cysticercus. Humans acquire the cysts through consumption of uncooked or under-cooked pork and the cysts grow into an adult worms in the small intestine.
Echinococcus granulosus, also called the hydatid worm or dog tapeworm, is a cyclophyllid cestode that dwells in the small intestine of canids as an adult, but which has important intermediate hosts such as livestock and humans, where it causes cystic echinococcosis, also known as hydatid disease. The adult tapeworm ranges in length from 3 mm to 6 mm and has three proglottids ("segments") when intact—an immature proglottid, mature proglottid and a gravid proglottid. The average number of eggs per gravid proglottid is 823. Like all cyclophyllideans, E. granulosus has four suckers on its scolex ("head"), and E. granulosus also has a rostellum with hooks. Several strains of E. granulosus have been identified, and all but two are noted to be infective in humans.
Echinococcus multilocularis, the fox tapeworm, is a small cyclophyllid tapeworm found extensively in the northern hemisphere. E. multilocularis, along with other members of the Echinococcus genus, produce diseases known as echinococcosis. Unlike E. granulosus,E. multilocularis produces many small cysts that spread throughout the internal organs of the infected animal. The resultant disease is called Alveolar echinococcosis, and is caused by ingesting the eggs of E. multilocularis.
Mebendazole (MBZ), sold under the brand name Vermox among others, is a medication used to treat a number of parasitic worm infestations. This includes ascariasis, pinworm infection, hookworm infections, guinea worm infections, hydatid disease, and giardia, among others. It is taken by mouth.
Fenbendazole is a broad spectrum benzimidazole anthelmintic used against gastrointestinal parasites including: giardia, roundworms, hookworms, whipworms, the tapeworm genus Taenia, pinworms, aelurostrongylus, paragonimiasis, strongyles, and strongyloides that can be administered to sheep, cattle, horses, fish, dogs, cats, rabbits, most reptiles, freshwater shrimp tanks as planaria and hydra treatments, as well as seals.
Diphyllobothriasis is the infection caused by tapeworms of the genus Diphyllobothrium.
Ancylostomiasis is a hookworm disease caused by infection with Ancylostoma hookworms. The name is derived from Greek ancylos αγκύλος "crooked, bent" and stoma στόμα "mouth".
Necatoriasis is the condition of infection by Necator hookworms, such as Necator americanus. This hookworm infection is a type of helminthiasis (infection) which is a type of neglected tropical disease.
Deworming is the giving of an anthelmintic drug to a human or animals to rid them of helminths parasites, such as roundworm, flukes and tapeworm. Purge dewormers for use in livestock can be formulated as a feed supplement that is eaten, a paste or gel that is deposited at the back of the animal's mouth, a liquid drench given orally, an injectable, or as a pour-on which can be applied to the animal's topline. In dogs and cats, purge dewormers come in many forms including a granular form to be added to food, pill form, chew tablets, and liquid suspensions.
Anthelmintics or antihelminthics are a group of antiparasitic drugs that expel parasitic worms (helminths) and other internal parasites from the body by either stunning or killing them and without causing significant damage to the host. They may also be called vermifuges or vermicides. Anthelmintics are used to treat people who are infected by helminths, a condition called helminthiasis. These drugs are also used to treat infected animals.
Coenurosis is a parasitic infection that results when humans ingest the eggs of dog tapeworm species Taenia multiceps, T. serialis, T. brauni, or T. glomerata.
Oxfendazole is a broad spectrum benzimidazole anthelmintic. Its main use is for protecting livestock against roundworm, strongyles and pinworms. Oxfendazole is the sulfoxide metabolite of fenbendazole.
Taenia hydatigena is one of the adult forms of the canine and feline tapeworm. This infection has a worldwide geographic distribution. Humans with taeniasis can infect other humans or animal intermediate hosts by eggs and gravid proglottids passed in the feces.
Cattle drenching is the process of administering chemical solutions (anthelmintics) to cattle or Bos taurus with the purpose of protecting livestock from various parasites including worms, fluke, cattle ticks, lice and flies. Parasites hinder the production of cattle through living off their host and carrying diseases that can be transmitted to cattle. Cattle drenches can be applied through a solution poured on the back, throat or an injection. Cattle drenches are predominately necessary for young cattle with weaker immune systems that are susceptible to parasite infestation. Drenching is a common method for controlling parasites in the meat and dairy industries. Drenching cattle improves the health, condition and fertility of cattle leading to increased calving rates, weight gain, hide condition and milk production.
Cat worm infections, the infection of cats (Felidae) with parasitic worms, occur frequently. Most worm species occur worldwide in both domestic and other cats, but there are regional, species and lifestyle differences in the frequency of infestation. According to the classification of the corresponding parasites in the zoological system, infections can be divided into those caused by nematode and flatworms - in the case of the latter, mainly cestoda and trematoda - while other strains are of no veterinary significance. While threadworms usually do not require an intermediate host for their reproduction, the development cycle of flatworms always proceeds via alternate hosts.