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Clinical particulars
Target species
Indications for use for each target species
For cats with, or at risk from mixed infections by cestodes, nematodes and ectoparasites. The veterinary medicinal product is exclusively indicated when all three groups are targeted at the same time.
- Treatment of infestations by fleas (Ctenocephalides felis). One treatment provides immediate and persistent flea killing activity for one month.
- The product can be used as part of a treatment strategy for the control of flea allergy dermatitis (FAD).
- Treatment of infestations by ticks. One treatment provides immediate and persistent tick killing activity against Ixodes scapularis for one month and against Ixodes ricinus for five weeks.
- Persistent tick killing activity from 7 days to five weeks after treatment against Rhipicephalus sanguineus.
- Persistent tick killing activity from 7 days to four weeks after treatment against Ixodes hexagonus.
- Treatment of infestations by ear mites (Otodectes cynotis).
- Treatment of Notoedric mange (caused by Notoedres cati).
Gastro-intestinal cestodes
- Treatment of infections with tapeworms (Dipylidium caninum, Taenia taeniaeformis, Echinococcus multilocularis, Joyeuxiella pasqualei and Joyeuxiella fuhrmanni).
Gastro-intestinal nematodes
- Treatment of infections with gastrointestinal nematodes (L3, L4 larvae and adults of Toxocara cati, L4 larvae and adults of Ancylostoma tubaeforme and Ancylostoma ceylanicum, and adult forms of Toxascaris leonina and Ancylostoma braziliense).
Cardio-pulmonary nematodes
- Prevention of heartworm disease (Dirofilaria immitis) for one month.
- Treatment of infections with feline lungworms (L4 larvae and adults of Troglostongulus brevior, L3, L4 larvae and adults of Aelurostrongylus abstrusus).
- Prevention of aelurostrongylosis (by reduction of the level of infection with L3, L4 larvae of Aelurostrongylus abstrusus).
Vesical nematodes
- Treatment of infections with vesical worms (Capillaria plica).
Do not use in cases of hypersensitivity to the active substances or to any of the excipients.
Special warnings for each target species
When applying the veterinary medicinal product, special attention should be paid to long hair breeds in order to ensure that the product is applied directly to the skin and not on the hair, as this could lead to a lower bioavailability of the active substance.
Ticks and fleas need to start feeding on the cat to become exposed to the esafoxolaner; therefore, the risk of transmission of arthropod borne diseases cannot be excluded.
Cats in endemic areas for heartworm, or those which have travelled to endemic areas, may be infected with adult heartworms. Although the veterinary medicinal product may be safely administered to cats infected with adult heartworms, no therapeutic effect against adult Dirofilaria immitis has been established. It is, therefore, recommended that all cats 6 months of age or older, living in endemic areas for heartworm, should be tested for existing adult heartworm infection before being treated with the product for heartworm disease prevention.
Tapeworm infection may reoccur unless control of intermediate hosts such as fleas, mice etc. is undertaken. Some cats with patent Joyeuxiella spp. or Dipylidium caninum infection may nevertheless harbour a high proportion of juvenile worms, which may be less susceptible to the product; therefore, a post-treatment follow-up is recommended in case of such infections.
Parasite resistance to any particular class of antiparasitics included in the fixed combination product may develop following repeated use of antiparasitics of those classes over an extended period of time. Therefore, epidemiological information about current susceptibility of the target species should be taken into account in order to limit the possibility of a future selection for resistance.
Unnecessary use of antiparasitics or use deviating from the instructions given in the SPC may increase the resistance selection pressure and lead to reduced efficacy. The decision to use the product should be based on confirmation of the parasitic species and burden, or of the risk of infestation based on its epidemiological features, for each individual animal.
In the absence of risk of co-infection, a narrow spectrum product should be used.
The possibility that other animals in the same household can be a source of re-infection with fleas or worms should be considered, and these should be treated as necessary with an appropriate product.
Avoid shampooing the animal within the 2 days following application because the effectiveness of the product in this case has not been tested.
To reduce re-infestation from emergence of new fleas, it is recommended that all cats in a household are treated. Other animal species living in the same household should also be treated with a suitable product.
All stages of fleas can infest the cat's basket, bedding and regular resting areas such as carpets and soft furnishings. In case of massive flea infestation and at the beginning of the control measures, these areas should be treated with a suitable environmental product and then vacuumed regularly.
Special precautions for use
Special precautions for safe use in target species:
Spot-on application only. Do not inject, do not administer orally or via any other route. Avoid contact with the cat's eyes. If accidental ocular contact occurs, flush the eyes immediately with clean water. If eye irritation persists, seek veterinary advice.
It is important to apply the veterinary medicinal product to a skin area where the cat cannot lick it off: on the midline of the neck, between the base of the skull and the shoulder blades. Ensure that animals do not lick each other until the treated area is no longer noticeable. Oral ingestion of the veterinary medicinal product has been observed to lead to hypersalivation.
The safety of the veterinary medicinal product has not been tested in kittens under 8 weeks of age. The product is for use in cats weighing at least 0.8 kg and from 8 weeks of age.
The veterinary medicinal product should exclusively be used in confirmed mixed infections or where cats are at significant risk of such mixed infection with ectoparasites and nematodes (including for heartworm disease prevention) and where concurrent treatment against cestodes is indicated. In the absence of risk of co-infestation, the use of a narrow spectrum parasiticide should be considered as a first line therapy.
The rationale for prescription and frequency of use should be tailored to the individual needs of the cat, based on clinical assessment, the animal's lifestyle and on the local epidemiological situation (including zoonotic risks, where relevant) in order to address exclusively situations of mixed infections/risk of infection.
The veterinary medicinal product should not be used in other cats without prior veterinary consultation.
Repeated treatments should be restricted to limited individual situations (see 'Amounts to be administered and administration route' for treatment guidance) with a minimum treatment interval of 4 weeks. The safety was not evaluated beyond 6 months (see also 'Special warnings for each target species', 'Overdose' and 'Pharmacokinetic particulars'), therefore no more than 6 consecutive treatments are recommended to be given within a 12-month period.
Echinococcosis represents a hazard for humans and is a notifiable disease to the World Organisation for Animal Health (WOAH). In case of echinococcosis, specific guidelines on the treatment and follow up and on the safeguard of persons have to be followed. Experts or institutes of parasitology should be consulted.
Special precautions to be taken by the person administering the veterinary medicinal product to animals
Do not smoke, drink or eat during application. Wash hands immediately after use. Used applicators should be disposed of immediately and not left within the sight or reach of children.
Avoid contact of the applicator content with the fingers. If this occurs, wash off with soap and water. This veterinary medicinal product can cause eye irritation, which might be in exceptional cases severe. In case of accidental eye exposure, flush the eyes immediately and thoroughly with water. Remove contact lenses, if present, after the first 5 minutes, and then continue rinsing. Seek medical advice and show the package leaflet or the label to the physician.
Ensure that the treated area is no longer noticeable before resuming contact with the site of application. Children should not be allowed to play with treated animals until the application site is no longer noticeable and it is recommended that recently treated animals do not sleep with owners, especially children. It is recommended to treat animals in the evening to reduce contact with people after treatment.
People with known hypersensitivity to esafoxolaner, eprinomectin or praziquantel or to any other of the excipients should avoid contact with the veterinary medicinal product. Since foetotoxic and teratogenic effects are described in laboratory animals after significant daily exposure to glycerol formal, pregnant women should wear gloves during the administration to avoid direct contact with the product.
Special precautions for the protection of the environment:
Not applicable.
Adverse events
(1 to 10 animals / 1 000 animals treated):
Hypersalivation1, diarrhoea1, emesis1
Application site alopecia1,2, application site pruritus1,2
Lethargy1, anorexia1
1 Mostly mild reactions, of short duration and self-limiting
2 Transient
Reporting adverse events is important. It allows continuous safety monitoring of a veterinary medicinal product. Reports should be sent, preferably via a veterinarian, to either the marketing authorisation holder or its local representative or the national competent authority via the national reporting system. See the package leaflet for respective contact details.
Use during pregnancy, lactation or lay
Pregnancy and lactation:
Can be used in pregnant and lactating queens.
Can be used in breeding queens
The safety of the veterinary medicinal product has not been established in breeding male cats. Laboratory studies in rats and rabbits have not produced any evidence of adverse effects of the active substances on the reproductive capacity in males. In breeding males, use only according to the benefit-risk assessment by the prescribing veterinarian.
Interaction with other medicinal products and other forms of interaction
None known.
Amounts to be administered and administration route
Spot-on use.
The recommended minimum doses are 1.44 mg esafoxolaner, 0.48 mg eprinomectin and 10 mg praziquantel per kg bodyweight. Select the appropriate applicator size for the weight of the cat.To ensure a correct dosage, body weight should be determined as accurately as possible. Underdosing could result in ineffective use and may favour resistance development.
Cat weight
Volume of unit dose (ml)
Esafoxolaner (mg)
Eprinomectin (mg)
Praziquantel (mg)
0.8 - <2.5 kg
2.5 - <7.5 kg
≥7.5 kg
appropriate combination of applicators
Method of administration:
1. Use scissors to cut the blister along the dotted line
2. Then pull the lid away.
3. Remove the applicator from the package and hold it upright. Pull back the plunger slightly.
4. Twist and pull off the cap.
5. Part the hair on the midline of the neck, between the base of the skull and the shoulder blades until the skin is visible. Place the tip of the applicator on the skin and apply the entire content directly onto the skin in one spot. The product should be applied to dry skin on an area where the cat cannot lick it off. In long hair breeds, special attention should be paid to apply the product onto the skin, and not on the hair to ensure optimal efficacy.
6. Wash your hands after use.
Treatment schedule:
For the treatment of infestations with fleas and/or ticks and/or mites, and the concurrent treatment of gastrointestinal and/or pulmonary, and/or vesical nematodes, and cestodes, a single dose of the product should be applied. The need for and frequency of re-treatment(s) should be in accordance with the advice of the prescribing veterinarian and should take into account the local epidemiological situation and the animal’s lifestyle (e.g. outdoors access). See also 'Special precautions for use'.
Areas which are not-endemic areas for heartworm or feline lungworm:
Cats not exposed to a permanent risk of heartworm or feline lungworm infection should be treated according to a schedule prescribed by the veterinarian and adapted to each individual situation of re-infection/-infestation with parasites. Otherwise, a narrow spectrum product should be used to ensure sustainable treatment against relevant parasites.
Heartworm endemic areas:
Cats living in heartworm endemic areas and recognised as hunters might be treated at monthly intervals to ensure both appropriate heartworm disease prevention and treatment of potential re-infection with cestodes. Otherwise, a narrow spectrum product should be used for further treatment. Prevention of heartworm disease by killing Dirofilaria immitis larvae should start within 1 month after the first expected exposure to mosquitoes and should be continued until at least 1 month after the last exposure to mosquitoes.
Feline lungworm endemic area:
Cats at risk (hunting behaviour) living in endemic areas might be treated at monthly intervals to decrease the risk of establishment of adult lungworms responsible for clinical aelurostrongylosis and to treat potential re-infection with cestodes. Otherwise, a narrow spectrum product should be used for further treatment.
Lungworm treatment: No or little effect on the L1 larvae release of A. abstrusus in the faeces can be expected within approximately 2 weeks after treatment due to the transit period of L1 larvae from the lungs through the digestive tract. Any faecal larval count to control effectiveness of treatment (and the decision if a second treatment with a narrow spectrum product is necessary) should, therefore, only be made two weeks after treatment at the earliest.
Ear mites:
For ear mites, seek further veterinary examination 4 weeks after treatment to determine whether an additional treatment with a narrow spectrum product is necessary.
Symptoms of overdose (and where applicable, emergency procedures and antidotes)
Safety has been evaluated with up to 5 times the maximum recommended dose in healthy kittens aged 8 weeks and older treated up to 6 times at 4-week intervals. At 3 times the maximum recommended dose, no undesirable effects were observed. At 5 times the maximum recommended dose, a single severe adverse neurological reaction (ataxia, disorientation, apathy, tremors, hypothermia and pupil dilation) was observed after the third treatment and was reversible following washing of the application site, emergency measures and symptomatic treatment. In some animals, at 5 times the maximum recommended dose, dark red subcutaneous areas at the skin treatment sites were observed.