{"product_id":"equiverm-duo-pasta-7-ml-x-1-sg-ivermectin-20-mg-praziquantel-100-mg-oral-paste-for-horse-cavalli","title":"EQUIVERM DUO PASTA 7 ML x 1 SG \/\/ Ivermectin 20 mg Praziquantel 100 mg \/\/ oral paste for horse \/ cavalli","description":"\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eEQUIVERM DUO\u003cbr\u003e\u003cbr\u003e\u003c\/span\u003e\u003c\/strong\u003eOral paste for horses.\u003cstrong\u003e\u003cspan\u003e\u003cbr\u003e\u003cbr\u003eComposition\u003cbr\u003e\u003c\/span\u003e\u003c\/strong\u003e1 ml of product contains:\u003cstrong\u003e\u003cspan\u003e\u003cbr\u003e\u003cbr\u003eActive substances:\u003cbr\u003e\u003c\/span\u003e\u003c\/strong\u003eIvermectin 20 mg\u003cbr\u003ePraziquantel 100 mg\u003cstrong\u003e\u003cspan\u003e\u003cbr\u003e\u003cbr\u003eExcipients:\u003cbr\u003e\u003c\/span\u003e\u003c\/strong\u003eButylated hydroxyanisole (E320) 0.2 mg\u003cstrong\u003e\u003cspan\u003e\u003cbr\u003e\u003cbr\u003eIndications\u003cbr\u003e\u003c\/span\u003e\u003c\/strong\u003eIt is indicated in the treatment of parasitic diseases caused by cestodes, nematodes or arthropods, sensitive to the antiparasitic action of Equiverm Duo oral paste, in horses:\u003cbr\u003eCestodes (adults):\u003cbr\u003eAnoplocephala perfoliata, Anoplocephala magna.\u003cbr\u003eLarge strongyles:\u003cbr\u003eStrongylus vulgaris (adult stages and arterial larval stages), Strongylus edentatus (adult stages and tissue larval stages), Strongylus equinus (adult stages), Triodontophorus spp. (adult stages), Triodontophorus brevicauda, ​​Triodontophorus serratus, Craterostomum acuticaudatum (adult stages)\u003cbr\u003eSmall strongilli or cyathostomes, adult stages and in developmental stages (fourth intraluminal larval stage), including benzimidazole-resistant strains:\u003cbr\u003eCoronocyclus spp., Coronocyclus coronatus, Coronocyclus labiatus, Coronocyclus labratus, Cyathostomum spp. (Cyathostomum catinatum, Cyathostomum pateratum), Cylicocyclus spp. (Cylicocyclus ashworthi, Cylicocyclus elongatus, Cylicocyclus insigne, Cylicocyclus leptostomum, Cylicocyclus nassatus), Cylicodontophorus spp. (Cylicodontophorus bicornatus), Cylicostephanus spp.\u003cbr\u003e(Cylicostephanus calicatus, Cylicostephanus goldi, Cylicostephanus longibursatus, Cylicostephanus minutus), Parapoteriostomum spp. (Parapoteriostomum mettami), Petrovinema spp. (Petrovinema poculatum), Poteriostomum spp.\u003cbr\u003eTrichostrongylus (adult stages): Trichostrongylus axei Pinworms (adult stages and fourth instar): Oxyuris equi Ascarids (adult stages, third and fourth larval stages): Parascaris equorum\u003cbr\u003eMicrofilariae: Onchocerca spp.\u003cbr\u003eIntestinal strongyles (adult stages): Strongyloides westeri\u003cbr\u003eGastric nematodes (adult stages): Habronema muscae\u003cbr\u003eGastrointestinal stages of gasterophile larvae: Gasterophilus spp.\u003cbr\u003eLung nematodes (adult stages and fourth instar): Dictyocaulus arnfieldi\u003cstrong\u003e\u003cspan\u003e\u003cbr\u003e\u003cbr\u003eContraindications\u003cbr\u003e\u003c\/span\u003e\u003c\/strong\u003eDo not use in horses with hypersensitivity to the active substances or to any of the excipients. The product is intended for use in horses only. The concentration of ivermectin in this product may cause adverse reactions in cats, dogs, especially Collies, Bobtails or related or cross breeds, and also in sea or freshwater turtles, if they ingest the product or come into contact with the applicator.\u003cstrong\u003e\u003cspan\u003e\u003cbr\u003e\u003cbr\u003eAdverse reactions\u003cbr\u003e\u003c\/span\u003e\u003c\/strong\u003eSome horses heavily infested with Onchocera microfilariae have shown post-treatment edema and pruritus, probably due to the destruction of a large number of microfilariae. These symptoms disappear within a few days and symptomatic treatment is necessary. In case of massive cestode infestations, signs of mild and transient colic, soft faeces may occur.\u003cbr\u003eIn rare cases, inflammation of the lips, mouth and tongue has been reported after administration, leading to various clinical symptoms such as edema, hypersalivation, erythema, tongue disorders and stomatitis. These reactions, which occur within one hour of administration and disappear within 24-48 hours, are transient. If more severe oral reactions occur, symptomatic treatment is recommended.\u003cbr\u003eIf you notice serious reactions or other effects not mentioned in this leaflet, please inform your veterinarian.\u003cstrong\u003e\u003cspan\u003e\u003cbr\u003e\u003cbr\u003eTarget species\u003cbr\u003e\u003c\/span\u003e\u003c\/strong\u003eHorses.\u003cstrong\u003e\u003cspan\u003e\u003cbr\u003e\u003cbr\u003eDosage for each species, route of administration and method of administration\u003cbr\u003eOral use.\u003cbr\u003e\u003c\/span\u003e\u003c\/strong\u003eThe recommended dose is 200 µg ivermectin and 1 mg praziquantel per kg body weight, which corresponds to a single dose of 1 ml of paste per 100 kg body weight. To ensure the correct dose is administered, the body weight of the animals should be determined as accurately as possible before treatment. The applicator is marked with divisions for administration in 100 increments of 100 kg body weight. The applicator should be adjusted to the calculated dose by fixing the ring to the appropriate position on the plunger.\u003cstrong\u003e\u003cspan\u003e\u003cbr\u003e\u003cbr\u003eRecommendations for correct administration\u003cbr\u003e\u003c\/span\u003e\u003c\/strong\u003eHold the applicator plunger, turn the dosage ring marked on the plunger so that the lower edge of the ring is aligned with the position for the desired weight. Make sure that the animal has no feed residue in its mouth. Remove the applicator cap, insert it into the horse’s mouth and administer the paste at the base of the tongue. After application, immediately raise the horse's head for a few seconds and ensure that the animal has swallowed the dose.\u003cstrong\u003e\u003cspan\u003e\u003cbr\u003e\u003cbr\u003eAntiparasitic program:\u003cbr\u003e\u003c\/span\u003e\u003c\/strong\u003eTo obtain an adequate level of protection against parasitic infestations, veterinary advice on the appropriate dosage and zoo-hygienic conditions is required.\u003cstrong\u003e\u003cspan\u003e\u003cbr\u003e\u003cbr\u003eWithdrawal period\u003cbr\u003e\u003c\/span\u003e\u003c\/strong\u003eMeat: 30 days.\u003cbr\u003eMilk: do not administer the product to mares producing milk for human consumption.\u003cstrong\u003e\u003cspan\u003e\u003cbr\u003e\u003cbr\u003eSpecial precautions for storage\u003cbr\u003e\u003c\/span\u003e\u003c\/strong\u003eKeep out of the reach and sight of children. Store below 25 °C. Keep the applicator tightly closed. Replace the cap after use. Do not use after the expiry date stated on the label. Shelf life after first opening the immediate packaging: 6 months.\u003cstrong\u003e\u003cspan\u003e\u003cbr\u003e\u003cbr\u003eSpecial warnings\u003cbr\u003e\u003c\/span\u003e\u003c\/strong\u003eSpecial warnings for each target species\u003cbr\u003eThe following practices should be avoided as they may increase the risk of resistance development and may ultimately result in ineffective treatment:\u003cbr\u003e− too frequent and repeated use of anthelmintics from the same class for a long period of time.\u003cbr\u003e−  Underdosing, which may be caused by underestimation of body weight or non-calibration of dosing devices.\u003cbr\u003eSuspected clinical cases of anthelmintic resistance should be further investigated by appropriate methods (ovocoproscopy, etc.);\u003cbr\u003eIf the test results clearly indicate the establishment of resistance to a particular anthelmintic, another anthelmintic from a different pharmacological class and with a different mode of action should be used.\u003cbr\u003eResistance to macrocyclic lactones (which include ivermectin) has been reported in Parascaris equorum in horses in the EU. Therefore, the use of the product should be based on local epidemiological information (region, farm) on the sensitivity of gastrointestinal nematodes and recommendations on the possibilities of limiting the emergence of anthelmintic resistance.\u003cstrong\u003e\u003cspan\u003e\u003cbr\u003e\u003cbr\u003eSpecial precautions for use in animals\u003cbr\u003e\u003c\/span\u003e\u003c\/strong\u003eThere are no studies to confirm the safety of using this product in foals less than 2 months old or in breeding stallions, so the use of the product in these categories of animals is not recommended.\u003cstrong\u003e\u003cspan\u003e\u003cbr\u003e\u003cbr\u003eSpecial precautions to be taken by the person administering the veterinary medicinal product to animals\u003cbr\u003e\u003c\/span\u003e\u003c\/strong\u003eDo not eat, drink or smoke while using the product.\u003cbr\u003eThis product may cause skin or eye irritation. Avoid contact with skin or eyes. In case of accidental contact with the product, wash the affected area immediately with plenty of water.\u003cbr\u003eIn case of accidental ingestion or eye irritation, seek medical advice immediately and show the package leaflet or the label to the doctor.\u003cbr\u003ePeople with known hypersensitivity to ivermectin, praziquantel or any of the excipients should administer the product with caution. Pregnant or lactating women should administer the product with caution.\u003cbr\u003ePersonal protective equipment consisting of protective gloves should be worn when handling the veterinary medicinal product.\u003cbr\u003e\u003cstrong\u003e\u003cspan\u003e\u003cbr\u003eUse during pregnancy or lactation\u003cbr\u003e\u003c\/span\u003e\u003c\/strong\u003eStudies conducted on laboratory animals have not revealed any teratogenic or embryotoxic effects of ivermectin\u003cbr\u003eor praziquantel administered at recommended doses during treatment.\u003cbr\u003eThe combination of ivermectin and praziquantel can be used after the first three months of gestation and during lactation. Due to the lack of clinical data on the early period of gestation, the product can be used during the first three months of gestation only after a benefit\/risk assessment by the veterinarian.\u003cstrong\u003e\u003cspan\u003e\u003cbr\u003e\u003cbr\u003eInteractions with other medicinal products and other forms of interaction\u003cbr\u003e\u003c\/span\u003e\u003c\/strong\u003eNo data are available.\u003cstrong\u003e\u003cspan\u003e\u003cbr\u003e\u003cbr\u003eOverdose (symptoms, emergency procedures, antidotes), if appropriate\u003cbr\u003e\u003c\/span\u003e\u003c\/strong\u003eNo adverse reactions were observed in 2-month-old foals and adult horses receiving doses up to 3 and 10 times the recommended dose, respectively.\u003cbr\u003eIn horses treated twice with ivermectin oral paste or once with doses 10 times the recommended dose of oral paste (e.g. 2 mg\/kg body weight), temporary reduced appetite, fever, ptyalism and visual disturbances were observed. All symptoms resolved within five days. No antidote has been identified, but symptomatic treatment may be beneficial.\u003cbr\u003e\u003cstrong\u003e\u003cspan\u003e\u003cbr\u003eIncompatibilities\u003cbr\u003e\u003c\/span\u003e\u003c\/strong\u003eNot applicable\u003cstrong\u003e\u003cspan\u003e\u003cbr\u003e\u003cbr\u003eSpecial precautions for the disposal of unused veterinary medicinal product or waste materials, if applicable\u003cbr\u003e\u003c\/span\u003e\u003c\/strong\u003eAny unused veterinary medicinal product or waste materials derived from the use of such veterinary medicinal products should be disposed of in accordance with local requirements.\u003cbr\u003eThe product should not be disposed of in watercourses as it is dangerous for fish and other aquatic organisms.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eEQUIVERM DUO\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cbr\u003e\u003cspan\u003ePasta orale per cavalli.\u003c\/span\u003e\u003cbr\u003e\u003cbr\u003e\u003cstrong\u003e\u003cspan\u003eComposizione\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003e1 ml di prodotto contiene:\u003c\/span\u003e\u003cbr\u003e\u003cbr\u003e\u003cstrong\u003e\u003cspan\u003ePrincipi attivi:\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eIvermectina 20 mg\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003ePraziquantel 100 mg\u003c\/span\u003e\u003cbr\u003e\u003cbr\u003e\u003cstrong\u003e\u003cspan\u003eEccipienti:\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eButilidrossianisolo (E320) 0,2 mg\u003c\/span\u003e\u003cbr\u003e\u003cbr\u003e\u003cstrong\u003e\u003cspan\u003eIndicazioni\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eÈ indicato nel trattamento delle malattie parassitarie causate da cestodi, nematodi o artropodi, sensibili all'azione antiparassitaria di Equiverm Duo pasta orale, nei cavalli:\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eCestodi (adulti):\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eAnoplocephala perfoliata, Anoplocephala magna.\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eGrandi strongili:\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eStrongylus vulgaris (stadi adulti e stadi larvali arteriosi), Strongylus edentatus (stadi adulti e stadi larvali tissutali), Strongylus equinus (stadi adulti), Triodontophorus spp. (stadi adulti), Triodontophorus brevicauda, ​​Triodontophorus serratus, Craterostomum acuticaudatum (stadi adulti)\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003ePiccoli strongilli o ciatostomi, stadi adulti e in fase di sviluppo (quarto stadio larvale intraluminale), compresi i ceppi resistenti al benzimidazolo:\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eCoronocyclus spp., Coronocyclus coronatus, Coronocyclus labiatus, Coronocyclus labratus, Cyathostomum spp. (Cyathostomum catinatum, Cyathostomum pateratum), Cylicocyclus spp. (Cylicocyclus ashworthi, Cylicocyclus elongatus, Cylicocyclus insigne, Cylicocyclus leptostomum, Cylicocyclus nassatus), Cylicodontophorus spp. (Cylicodontophorus bicornatus), Cylicostephanus spp.\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003e(Cylicostephanus calicatus, Cylicostephanus goldi, Cylicostephanus longibursatus, Cylicostephanus minutus), Parapoteriostomum spp. (Parapoteriostomum mettami), Petrovinema spp. (Petrovinema poculatum), Poteriostomum spp.\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eTrichostrongylia (stadi adulti): Trichostrongylus axei Ossiuri (stadi adulti e quarto stadio di sviluppo): Oxyuris equi Ascaris (stadi adulti, terzo e quarto stadio di sviluppo larvale): Parascaris equorum\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eMicrofilarie: Onchocerca spp.\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eStrongili intestinali (stadi adulti): Strongyloides westeri\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eNematodi gastrici (stadi adulti): Habronema muscae\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eStadi gastrointestinali delle larve di gastrofili: Gasterophilus spp.\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eNematodi polmonari (adulti e quarto stadio): Dictyocaulus arnfieldi\u003c\/span\u003e\u003cbr\u003e\u003cbr\u003e\u003cstrong\u003e\u003cspan\u003eControindicazioni\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eNon usare in cavalli con ipersensibilità ai principi attivi o ad uno qualsiasi degli eccipienti. Il prodotto è destinato esclusivamente all'uso sui cavalli. La concentrazione di ivermectina contenuta in questo prodotto può causare reazioni avverse in gatti, cani, in particolare Collie, Bobtail o razze affini o incrociate e anche nelle tartarughe marine o d'acqua dolce se ingeriscono il prodotto o entrano in contatto con l'applicatore.\u003c\/span\u003e\u003cbr\u003e\u003cbr\u003e\u003cstrong\u003e\u003cspan\u003eReazioni avverse\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eAlcuni cavalli gravemente infestati da Onchocera microfilarie hanno mostrato edema e prurito post-trattamento, probabilmente dovuti alla distruzione di un gran numero di microfilarie. Questi sintomi scompaiono entro pochi giorni ed è necessario un trattamento sintomatico. In caso di infestazioni massicce di cestodi possono comparire segni di coliche lievi e transitorie e feci molli.\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eIn rari casi, dopo la somministrazione sono stati segnalati infiammazioni delle labbra, della bocca e della lingua, con conseguenti vari sintomi clinici quali edema, ipersalivazione, eritema, disturbi della lingua e stomatite. Queste reazioni, che compaiono entro un'ora dalla somministrazione e scompaiono entro 24-48 ore, sono transitorie. Se si verificano reazioni orali più gravi, si raccomanda un trattamento sintomatico.\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eSe notate reazioni gravi o altri effetti non menzionati in questo foglio illustrativo, informate il vostro veterinario.\u003c\/span\u003e\u003cbr\u003e\u003cbr\u003e\u003cstrong\u003e\u003cspan\u003eSpecie di destinazione\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eCavalli.\u003c\/span\u003e\u003cbr\u003e\u003cbr\u003e\u003cstrong\u003e\u003cspan\u003eDosaggio per ciascuna specie, via di somministrazione e modalità di somministrazione\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eSomministrazione orale.\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eLa dose consigliata è di 200 µg di ivermectina e 1 mg di praziquantel per kg di peso corporeo, che corrisponde ad una singola dose di 1 ml di pasta per 100 kg di peso corporeo. Per garantire la somministrazione di una dose corretta, il peso corporeo degli animali deve essere determinato nel modo più accurato possibile prima del trattamento. L'applicatore ha divisioni contrassegnate per la somministrazione da 100 a 100 kg di peso corporeo. L'applicatore deve essere regolato alla dose calcolata fissando l'anello nell'apposita posizione sul pistone.\u003c\/span\u003e\u003cbr\u003e\u003cbr\u003e\u003cstrong\u003e\u003cspan\u003eRaccomandazioni per una corretta somministrazione\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eTenere lo stantuffo dell'applicatore, ruotare l'anello contrassegnato con il dosaggio sullo stantuffo in modo che il bordo inferiore dell'anello sia allineato con la posizione del peso desiderato. Assicurarsi che l'animale non abbia resti di cibo in bocca. Rimuovere il cappuccio dell'applicatore, inserirlo nella bocca del cavallo e somministrare la pasta alla base della lingua. Dopo l'applicazione sollevare immediatamente la testa del cavallo per qualche secondo e assicurarsi che l'animale abbia ingerito la dose.\u003c\/span\u003e\u003cbr\u003e\u003cbr\u003e\u003cstrong\u003e\u003cspan\u003eProgramma antiparassitario:\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003ePer ottenere un adeguato livello di protezione contro le infestazioni parassitarie è necessario fornire consulenza veterinaria sul giusto dosaggio e sulle condizioni zooigieniche.\u003c\/span\u003e\u003cbr\u003e\u003cbr\u003e\u003cstrong\u003e\u003cspan\u003eTempo di attesa\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eCarne: 30 giorni.\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eLatte: il prodotto non verrà somministrato a cavalle che producono latte destinato al consumo umano.\u003c\/span\u003e\u003cbr\u003e\u003cbr\u003e\u003cstrong\u003e\u003cspan\u003ePrecauzioni particolari per la conservazione\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eTenere fuori dalla portata e dalla vista dei bambini. Conservare a temperatura inferiore a 25 °C. Tenere l'applicatore ben chiuso. Riposizionare il tappo dopo l'uso. Non utilizzare dopo la data di scadenza riportata sull'etichetta. Periodo di validità dopo la prima apertura dell'imballaggio primario: 6 mesi.\u003c\/span\u003e\u003cbr\u003e\u003cbr\u003e\u003cstrong\u003e\u003cspan\u003eAvvertenze speciali\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eAvvertenze speciali per ciascuna specie di destinazione\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eVerranno evitate le seguenti pratiche che potrebbero aumentare il rischio di sviluppare resistenza e potrebbero, in definitiva, comportare l'inefficacia del trattamento:\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003e− uso troppo frequente e ripetuto di antielmintici della stessa classe, per un lungo periodo di tempo.\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003e- \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e Sottodosaggio,\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e che può essere causato da una sottostima del peso corporeo o dalla mancata calibrazione dei dispositivi di dosaggio.\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eI casi clinici sospetti di resistenza antielmintica devono essere ulteriormente approfonditi con metodiche appropriate (ovocoproscopia, ecc.);\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eSe i risultati del test indicano chiaramente l'instaurarsi di resistenza ad un determinato antielmintico, verrà utilizzato un altro antielmintico di una classe farmacologica diversa e con una diversa modalità d'azione.\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eLa resistenza ai lattoni macrociclici (che includono l'ivermectina) è stata segnalata in Parascaris equorum nei cavalli nell'UE. Pertanto, l'uso del prodotto si baserà sulle informazioni epidemiologiche locali (regione, azienda agricola) riguardanti la sensibilità dei nematodi gastrointestinali e sulle raccomandazioni sulle possibilità di limitare l'insorgenza di resistenza agli antielmintici.\u003c\/span\u003e\u003cbr\u003e\u003cbr\u003e\u003cstrong\u003e\u003cspan\u003ePrecauzioni speciali per l'impiego negli animali\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eNon ci sono studi che confermino la sicurezza dell'uso di questo prodotto nei puledri di età inferiore a 2 mesi o negli stalloni riproduttori, pertanto l'uso del prodotto in queste categorie di animali non è raccomandato.\u003c\/span\u003e\u003cbr\u003e\u003cbr\u003e\u003cstrong\u003e\u003cspan\u003ePrecauzioni speciali che devono essere adottate dalla persona che somministra il medicinale veterinario agli animali\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eNon consumare cibi o bevande e non fumare durante l'utilizzo del prodotto.\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eQuesto prodotto può causare irritazione alla pelle o agli occhi. Evitare il contatto con la pelle o gli occhi. In caso di contatto accidentale con il prodotto, lavare immediatamente la zona interessata con abbondante acqua.\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eIn caso di ingestione accidentale o irritazione agli occhi consultare immediatamente un medico e mostrargli il foglio illustrativo o l'etichetta del prodotto.\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eLe persone con nota ipersensibilità all'ivermectina, al praziquantel o ad uno qualsiasi degli eccipienti devono usare il prodotto con cautela. Le donne in gravidanza o in allattamento devono somministrare il prodotto con attenzione.\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eDurante la manipolazione del medicinale veterinario è necessario indossare dispositivi di protezione individuale costituiti da guanti protettivi.\u003c\/span\u003e\u003cbr\u003e\u003cbr\u003e\u003cstrong\u003e\u003cspan\u003eUso durante la gravidanza o l'allattamento\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eStudi condotti su animali da laboratorio non hanno rivelato effetti teratogeni o embriotossici dell'ivermectina o del praziquantel somministrati alle dosi raccomandate durante il trattamento\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003e.\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eL'associazione di ivermectina e praziquantel può essere utilizzata dopo i primi tre mesi di gravidanza e durante l'allattamento. A causa dell'assenza di dati clinici sulle fasi iniziali della gravidanza, il prodotto può essere utilizzato durante i primi tre mesi di gravidanza solo dopo la valutazione del rapporto beneficio\/rischio da parte del veterinario.\u003c\/span\u003e\u003cbr\u003e\u003cbr\u003e\u003cstrong\u003e\u003cspan\u003eInterazioni con altri medicinali veterinari ed altre forme d'interazione\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eNessun dato disponibile.\u003c\/span\u003e\u003cbr\u003e\u003cbr\u003e\u003cstrong\u003e\u003cspan\u003eSovradosaggio (sintomi, procedure d’emergenza, antidoti), a seconda dei casi\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eNon sono state osservate reazioni avverse nei puledri di 2 mesi e nei cavalli adulti che hanno ricevuto dosi rispettivamente fino a 3 e 10 volte la dose raccomandata.\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eI cavalli trattati due volte con ivermectina pasta orale o una volta con dosi pari a 10 volte la dose raccomandata di pasta orale (ad esempio 2 mg\/kg di peso corporeo) hanno manifestato una temporanea riduzione dell'appetito, febbre, ptialismo e disturbi visivi. Tutti i sintomi sono scomparsi entro cinque giorni. Non è stato identificato alcun antidoto, ma il trattamento sintomatico può essere utile.\u003c\/span\u003e\u003cbr\u003e\u003cbr\u003e\u003cstrong\u003e\u003cspan\u003eIncompatibilità\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eNon applicabile\u003c\/span\u003e\u003cbr\u003e\u003cbr\u003e\u003cstrong\u003e\u003cspan\u003ePrecauzioni speciali per lo smaltimento del prodotto non utilizzato o dei rifiuti, a seconda dei casi\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eQualsiasi medicinale veterinario non utilizzato o i rifiuti derivanti dal suo utilizzo devono essere smaltiti in conformità con i requisiti locali.\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eIl prodotto non deve essere gettato nei corsi d'acqua in quanto pericoloso per i pesci e gli altri organismi acquatici.\u003c\/span\u003e\u003c\/p\u003e","brand":"Bioveta","offers":[{"title":"Default Title","offer_id":49968676405595,"sku":"","price":36.99,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0476\/3261\/3543\/files\/Equiverm_Duo_Pasta.jpg?v=1738084874","url":"https:\/\/www.petshopluna.com\/products\/equiverm-duo-pasta-7-ml-x-1-sg-ivermectin-20-mg-praziquantel-100-mg-oral-paste-for-horse-cavalli","provider":"Pet Shop Maya","version":"1.0","type":"link"}