Broadline spot-on solution for cats between 2.5 and 7.5 kg 3 pipettes
For cats with, or at risk from mixed infestations by cestodes, nematodes and ectoparasites
BROADLINE spot-on solution for cats 2.5-7.5 kg
2. QUALITATIVE AND QUANTITATIVE COMPOSITION
Each unit dose applicator delivers:
BROADLINE spot-on solution for Cats 2.5–7.5 kg :
Volume of unit dose: 0.9 ml
FIPRONIL : 74.7 mg
(S)-METHOPRENE : 90 mg
EPRINOMECTINE : 3.6 mg
PRAZIQUANTEL : 74.7 mg
Butylhydroxytoluene (E321) 1 mg/ml.
For the full list of excipients, see section 6.1.
3. PHARMACEUTICAL FORM
Clear colourless to yellow solution.
4. CLINICAL PARTICULARS
4.1 Target species
4.2 Indications for use, specifying the target species
For cats with, or at risk from mixed infestations by cestodes, nematodes and ectoparasites. The veterinary medicinal product is exclusively indicated when all three groups are targeted at the same time.
Treatment and prevention of infestations by fleas (Ctenocephalides felis). Elimination of fleas within 24 hours. One treatment prevents further infestations for at least one month.
Prevention of environmental flea contamination by inhibiting the development of flea immature stages (eggs, larvae and pupae) for over a month.
The product can be used as part of a treatment strategy for the control of flea allergy dermatitis (FAD).
Treatment and prevention of infestations by ticks (Ixodes ricinus). Elimination of ticks within 48 hours. One treatment prevents further infestations for up to 3 weeks.
Treatment of notoedric mange (Notoedres cati).
Treatment of infestations with tapeworms (Dipylidium caninum, Taenia taeniaeformis, Echinococcus multilocularis).
Treatment of infestations with gastrointestinal nematodes (L3, L4 larvae and adults of Toxocara cati, L4 larvae and adults of Ancylostoma tubaeforme, and adult forms of Toxascaris leonina and Ancylostoma brazilienze).
Treatment of infestations with feline lungworm (L3 larvae, L4 larvae and adults of Aelurostrongylus abstrusus).
Treatment of infestations with vesical worms (Capillaria plica).
Prevention of heartworm disease (Dirofilaria immitis larvae) for one month.
Do not use in sick or convalescent animals.
Do not use in rabbits.
Do not use in cases of hypersensitivity to the active substances or to any of the excipients.
4.4 Special warnings for each target species
When applying the veterinary medicinal product, special attention should be paid in long hair breeds in order to ensure that it is applied directly to the skin and not on the hair, as this could lead to a lower bioavailability of the active substances and thus, to a reduced efficacy.
It is important to apply the veterinary medicinal product to a skin area where the cat cannot lick it off. Avoid animals licking each other following treatment.
No data on the effect of bathing/shampooing on the efficacy of the veterinary medicinal product in cats is available. However, brief contact of the animal with water on one or two occasions within the month following application is unlikely to significantly reduce its efficacy. As a precaution, it is not recommended to bathe animals within 2 days after topical treatment.
After treatment with BROADLINE, ticks will generally be killed within 48 hours after infestation without having a blood meal. However, since the attachment of single ticks after treatment cannot be excluded transmission of infectious diseases cannot be completely ruled out.
Tapeworm infestation may reoccur unless control of intermediate hosts such as fleas, mice etc. is undertaken.
In certain individual cats Notoedres cati infestation may be severe or complicated by bacterial infections. In these severe cases concomitant treatment may be necessary.
Parasite resistance to any particular class of antiparasitic drug may develop following frequent use of a compound of that class. 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.
Cats in areas endemic 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 more, living in areas endemic for heartworm, should be tested for existing adult heartworm infestation before being treated with the product for heartworm prevention.
4.5 Special precautions for use
Special precautions for use in animals
Spot-on application only. Do not inject, do not administer orally or via any other route. Avoid contact with the cat's eyes.
The safety of the veterinary medicinal product has not been tested at intervals of less than 2 weeks or in kittens weighing less than 0.6 kg and/or under 7 weeks of age.
The veterinary medicinal product is not intended for use in dogs. Some dog breeds may present increased susceptibility to macrocyclic lactones, potentially leading to signs of neurotoxicity. Oral uptake by Collies, Old English Sheepdogs and related breeds or crossbreeds should thus be avoided.
Echinococcosis represents a hazard for humans, and is a notifiable disease to the World Organisation for Animal Health (OIE).
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 after use.
Unused applicators must be stored in the intact blister package.
Avoid contact of the applicator content with the fingers. If this occurs, wash off with soap and water. In case of accidental eye exposure, flush the eyes thoroughly with water as the product can cause slight mucous membrane and eye irritation. If eye irritation persists or if side effects are noted, seek medical advice and show the package leaflet or the label to the physician.
Handling of treated animals should be limited until the application site is dry, and children should not be allowed to play with treated animals during this period. It is therefore recommended that recently treated animals do not sleep with owners, especially children.
People with a known hypersensitivity to any of the active ingredients or excipients should avoid contact with the veterinary medicinal product.
4.6 Adverse reactions (frequency and seriousness)
A temporary clumping or spiking of the hair may be seen at the application site after treatment. Mild and transient skin reactions at the application site (itching, hair loss) may occur.
If the cat licks the application site after treatment, temporary excessive salivation can be observed. Oral ingestion of the veterinary medicinal product may also result in vomiting and/or in transient neurological signs such as ataxia, disorientation, apathy and pupil dilation.
All these signs resolve spontaneously within 24 hours. Correct application will minimise the occurrence of such events (see section 4.9).
4.7 Use during pregnancy, lactation or lay
The safety of the veterinary medicinal product has not been established during pregnancy and lactation. Laboratory studies with the individual ingredients in rats and rabbits have not produced teratogenic, foetotoxic or maternotoxic effects. Use only according to the benefit-risk assessment by the prescribing veterinarian.
4.8 Interaction with other medicinal products and other forms of interaction
4.9 Amounts to be administered and administration route
The use of the veterinary medicinal product should exclusively be based on the confirmed mixed infestations or significant risk of such mixed infestation 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 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 infestations/risk of infestation.
Treatment should not be extrapolated from one animal to the other without veterinary opinion.
The recommended minimum doses are 10 mg/kg bodyweight for fipronil, 12 mg/kg for (S)methoprene, 0.5 mg/kg for eprinomectin and 10 mg/kg for praziquantel.
Select the appropriate applicator size for the weight of the cat.
BROADLINE spot-on solution for Cats < 2,5 kg :
Volume of unit dose: 0.3 ml
FIPRONIL : 24.9 mg
(S)-METHOPRENE : 30 mg
EPRINOMECTINE : 1.2 mg
PRAZIQUANTEL : 24.9 mg
BROADLINE spot-on solution for Cats 2.5–7.5 kg :
Volume of unit dose: 0.9 ml
FIPRONIL : 74.7 mg
(S)-METHOPRENE : 90 mg
EPRINOMECTINE : 3.6 mg
PRAZIQUANTEL : 74.7 mg
For Cats > 7.5 kg:
appropriate combination of applicators
Method of administration:
Use a pair of scissors to cut the blister along the dotted line, then pull the lid away.
Remove the applicator from the package and hold it upright. Pull back the plunger slightly, twist and pull off the cap. 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.
Prevention of heartworm disease (Dirofilaria immitis larvae) should start within 1 month after the first expected exposure to mosquitoes.
For treatment against Aelurostrongylus abstrusus, a second administration one month after the initial treatment may be recommended.
4.10 Overdose (symptoms, emergency procedures, antidotes), if necessary
Safety has been demonstrated with up to 5 times the maximum exposure dose (i.e. up to 15 times the recommended dose) in healthy kittens aged 7 weeks and older treated up to 6 times at four-week intervals. It has also been confirmed in healthy adult cats treated 3 times at two-week intervals with up to 5 times the recommended doses. Mild and transient neurological signs such as ataxia, disorientation, apathy and pupil dilation may be observed, with spontaneous recovery the day after. Transient salivation and/or vomiting could also be observed, both in kittens and adult cats, in isolated cases.
Cats infected with adult heartworms tolerated up to 3 times the maximum exposure dose (i.e. up to 9 times the recommended dose), every 4 weeks for 3 treatments, without any adverse effects.
4.11 Withdrawal period
5. PHARMACOLOGICAL PROPERTIES
Pharmacotherapeutic group: antiparasitic products, insecticides, avermectins, eprinomectin in combinations.
ATCvet code: QP54AA54.
The veterinary medicinal product is a spot-on solution for topical use containing the insecticidal and acaricidal active ingredients fipronil (adulticide) and (S)-methoprene (ovicidal and larvicidal), combined with the endectocide eprinomectin and the cestocide praziquantel to complete the broad spectrum with activity against gastrointestinal nematodes, lungworms and tapeworms, and vesical worms.
5.1 Pharmacodynamic properties
Fipronil is an insecticide and acaricide belonging to the phenylpyrazole family. Fipronil and its metabolite fipronil sulfone act at ligand-gated chloride channels, in particular those gated by the neurotransmitter gamma-aminobutyric acid (GABA) as well as desensitising (D) and non- desensitising (N) channels gated by glutamate (Glu, unique invertebrate ligand-gated chloride channels), thereby blocking pre- and post-synaptic transfer of chloride ions across cell membranes. This results in uncontrolled activity of the central nervous system and death of insects or acarians.
(S)-Methoprene is an insect growth regulator (IGR) of the class of compounds known as juvenile hormone analogues that inhibit the development of immature stages of insects. This compound mimics the action of juvenile hormone and causes impaired development and death of the developing stages of fleas. The on-animal ovicidal activity of (S)-methoprene results from either direct penetration of the eggshell of newly laid eggs or from absorption through the cuticle of the adult fleas. (S)-Methoprene is also effective in preventing flea larvae and pupae from developing, which prevents contamination of the environment of the treated animals with the immature stages of fleas.
Eprinomectin is a member of the macrocyclic lactone class of endectocides. Compounds of the class bind selectively and with high affinity to glutamate-gated chloride ion channels which occur in invertebrate nerve or muscle cells. This leads to an increase in the permeability of the cell membrane to chloride ions with hyperpolarisation of the nerve or muscle cell, resulting in paralysis and death of the parasite. The spectrum of efficacy of eprinomectin has been shown to cover gastrointestinal and extraintestinal nematodes.
Praziquantel is a synthetic isoquinoline-pyrazine derivative with activity against tapeworms. Praziquantel is rapidly adsorbed via the surface of the parasites and affects membrane permeability in cestodes, influencing divalent cation fluxes, particularly calcium ion homeostasis, which is thought to contribute to the rapid muscle contraction and vacuolisation. This results in severe damage to the parasite integument, contraction and paralysis, disruption of metabolism and finally leads to the death and expulsion of the parasite. Disintegrated and partially digested fragments may occasionally be seen in the faeces.
5.2 Pharmacokinetic particulars
The ectoparasitic activity of fipronil and (S)-methoprene is mediated by direct contact with the ectoparasites rather than by systemic exposure. After a single topical application of the veterinary medicinal product, the actives were detected at various regions of the cat’s body, including the caudal region, within the first days of application, indicating distribution/movement from the site of application (between the head and shoulder blades) across the body of the animal. Fipronil sulfone, as a photodegradation product of fipronil, is also found on the hair. The concentrations in the hair coat of fipronil, fipronil sulfone and (S)-methoprene decrease with time but remain detectable for at least 42 days after dosing. The topical application, with additional potential oral exposure from grooming, also results in partial systemic exposure that decreases over time.
The peak plasma concentrations of the absorbed fraction of fipronil and (S)-methoprene are reached in 8 to 9 hours. Unlike other species, fipronil sulfone is not formed in cat. Fipronil is mainly excreted in the faeces as unchanged drug. (S)-methoprene, once absorbed, is very quickly metabolized and excreted.
Eprinomectin and praziquantel act systemically, with plasma concentrations reaching a maximum within 48 hours and 6 hours after treatment, respectively, reaching mean maximum concentrations (Cmax) of 20.1 ng/ml for eprinomectin and 157 ng/ml for praziquantel.
Once absorbed, eprinomectin is highly bound to plasma proteins (> 99%), has low clearance from blood, and distributes well into tissues. Its metabolism is limited, and it is mainly excreted unchanged in the faeces. The average half-life for this compound is 4.75 days. Praziquantel has a moderate tissue distribution, and about 64–84% of praziquantel is bound to plasma proteins. Praziquantel undergoes hepatic metabolism followed by renal excretion. The average half-life for praziquantel is 3.08 days.
In vitro metabolism assays and in vivo studies have demonstrated that there are no pharmacodynamic or pharmacokinetic interactions between fipronil, (S)-methoprene, eprinomectin and praziquantel.
6. PHARMACEUTICAL PARTICULARS
6.1 List of excipients
Disodium edetate (E385)
Propyl gallate (E310)
6.3 Shelf life
Shelf life of the veterinary medicinal product as packaged for sale: 2 years.
6.4 Special precautions for storage
Store in the original package in order to protect from light.