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actavis pharma, inc. - ivermectin (unii: 8883yp2r6d) (ivermectin - unii:8883yp2r6d) - ivermectin cream, 1% is indicated for the treatment of inflammatory lesions of rosacea. none. risk summary the available data on the use of ivermectin, including ivermectin cream, in pregnant women are insufficient to establish a drug- associated risk of major birth defects, miscarriage, or adverse maternal or fetal outcomes. in animal reproduction studies, ivermectin induced adverse developmental outcomes when orally administered to pregnant rats and rabbits during the period of organogenesis at doses 1909 or 354 times the maximum recommended human dose (mrhd), respectively. these orally administered doses were maternally toxic to pregnant rats and rabbits. in a pre-and postnatal developmental study in rats, neonatal toxicity and adverse effects on behavioral development were observed when ivermectin was orally administered to pregnant females during gestation and lactation (see data ). the background risk of major birth defects and miscarriage for the indicated population is unknown. all pregnancies have a

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covetrus north america - ivermectin (unii: 8883yp2r6d) (ivermectin - unii:8883yp2r6d) - indications : consult your veterinarian for assistance in the diagnosis, treatment, and control of parasitism. ivermectin paste provides effective treatment and control of the following parasites in horses.  large strongyles (adults) – strongylus vulgaris (also early forms in blood vessels), s . edentatus (also tissue stages), s . equinus , triodontophorus spp. including t . brevicauda and t . serratus and craterostomum acuticaudatum ; small strongyles (adults, including those resistant to some benzimidazole class compounds) – coronocyclus spp. including c . coronatus , c . labiatus and c . labratus , cyathostomum spp. including c . catinatum and c . pateratum , cylicocyclus spp. including c . insigne , c . leptostomum , c . nassatus and c . brevicapsulatus , cylicodontophorus spp., cylicostephanus spp. including c . calicatus , c . goldi , c . longibursatus and c . minutus , and petrovinema poculatum ; small strongyles – fourth-stage larvae; p

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viona pharmaceuticals inc - ivermectin (unii: 8883yp2r6d) (ivermectin - unii:8883yp2r6d) - ivermectin cream is indicated for the treatment of inflammatory lesions of rosacea. none. there are no adequate and well-controlled studies in pregnant women. ivermectin cream should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. note: the animal multiples of human exposure calculations were based on auc comparisons. the maximum topical human dose (mthd) of ivermectin cream is 1 g applied once daily. risk summary the available data on the use of ivermectin, including ivermectin cream, in pregnant women are insufficient to establish a drug- associated risk of major birth defects, miscarriage, or adverse maternal or fetal outcomes. in animal reproduction studies, ivermectin induced adverse developmental outcomes when orally administered to pregnant rats and rabbits during the period of organogenesis at doses 1909 or 354 times the maximum recommended human dose (mrhd), respectively. these orally administered doses were maternally toxic to pregnant rats and rabbi

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merck sharp & dohme llc - ivermectin (unii: 8883yp2r6d) (ivermectin - unii:8883yp2r6d) - ivermectin 3 mg - stromectol is indicated for the treatment of the following infections: strongyloidiasis of the intestinal tract . stromectol is indicated for the treatment of intestinal (i.e., nondisseminated) strongyloidiasis due to the nematode parasite strongyloides stercoralis . this indication is based on clinical studies of both comparative and open-label designs, in which 64-100% of infected patients were cured following a single 200-mcg/kg dose of ivermectin. (see clinical pharmacology, clinical studies.) onchocerciasis . stromectol is indicated for the treatment of onchocerciasis due to the nematode parasite onchocerca volvulus . this indication is based on randomized, double-blind, placebo-controlled and comparative studies conducted in 1427 patients in onchocerciasis-endemic areas of west africa. the comparative studies used diethylcarbamazine citrate (dec-c). note: stromectol has no activity against adult onchocerca volvulus parasites. the adult parasites reside in subcutaneous nodules which are infrequently palpable. surgical excision of these nodules (nodulectomy) may be considered in the management of patients with onchocerciasis, since this procedure will eliminate the microfilariae-producing adult parasites. stromectol is contraindicated in patients who are hypersensitive to any component of this product.

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padagis us llc - ivermectin (unii: 8883yp2r6d) (ivermectin - unii:8883yp2r6d) - ivermectin cream is indicated for the treatment of inflammatory lesions of rosacea. none. risk summary the available data on the use of ivermectin, including lvermectin cream, in pregnant women are insufficient to establish a drug- associated risk of major birth defects, miscarriage, or adverse maternal or fetal outcomes. in animal reproduction studies, ivermectin induced adverse developmental outcomes when orally administered to pregnant rats and rabbits during the period of organogenesis at doses 1909 or 354 times the maximum recommended human dose (mrhd), respectively. these orally administered doses were maternally toxic to pregnant rats and rabbits. in a pre-and postnatal developmental study in rats, neonatal toxicity and adverse effects on behavioral development were observed when lvermectin was orally administered to pregnant females during gestation and lactation (see data ). the background risk of major birth defects and miscarriage for the indicated population is unknown. all pregnancies have a

United States - English - NLM (National Library of Medicine)

bryant ranch prepack - ivermectin (unii: 8883yp2r6d) (ivermectin - unii:8883yp2r6d) - ivermectin is indicated for the treatment of the following infections: ivermectin is indicated for the treatment of intestinal (i.e., nondisseminated) strongyloidiasis due to the nematode parasite strongyloides stercoralis . this indication is based on clinical studies of both comparative and open-label designs, in which 64-100% of infected patients were cured following a single 200-mcg/kg dose of ivermectin (see clinical pharmacology, clinical studies). ivermectin is indicated for the treatment of onchocerciasis due to the nematode parasite onchocerca volvulus . this indication is based on randomized, double-blind, placebo-controlled and comparative studies conducted in 1427 patients in onchocerciasis-endemic areas of west africa. the comparative studies used diethylcarbamazine citrate (dec-c). note: ivermectin has no activity against adult onchocerca volvulus parasites. the adult parasites reside in subcutaneous nodules which are infrequently palpable. surgical excision of these nodules (nodulectomy) may b

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durvet, inc. - ivermectin (unii: 8883yp2r6d) (ivermectin - unii:8883yp2r6d) - cattle: ivermectin injection is indicated for the effective treatment and control of the following harmful species of gastrointestinal roundworms, lungworms, grubs, sucking lice, and mange mites in cattle: gastrointestinal roundworms (adults and fourth-stage larvae): ostertagia ostertagi (including inhibited o. ostertagi) o. lyrata haemonchus placei trichostrongylus axei t. colubriformis cooperia oncophora c. punctata c. pectinata oesophagostomum radiatum bunostomum phlebotomum nematodirus helvetianus (adults only) n. spathiger (adults only) lungworms (adults and fourth-stage larvae): dictyocauius viviparus cattle grubs (parasitic stages): hypoderma bovis h. lineatum sucking lice: linognathus vituli haematopinus eurysternus solenopotes capillatus mites (scabies): psoroptes ovis (syn. p communis var. bovis ) sarcoptes scabiei var. bovis ivermectin injection has been proved to effectively control infections and to protect cattle from reinfection with dictyocaulus viviparus and oesophagostomum radiat

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virbac ah, inc - ivermectin (unii: 8883yp2r6d) (ivermectin - unii:8883yp2r6d), pyrantel pamoate (unii: 81bk194z5m) (pyrantel - unii:4qih0n49e7) - indications: for use in dogs to prevent canine heartworm disease by eliminating the tissue stage of heartworm larvae (dirofilaria immitis) for a month (30 days) after infection and for the treatment and control of roundworms (toxocara canis, toxascaris leonina) and hookworms (ancylostoma caninum, uncinaria stenocephala, ancylostoma braziliense).

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aspen veterinary resources, ltd. - ivermectin (unii: 8883yp2r6d) (ivermectin - unii:8883yp2r6d) - ivermectin 5 mg in 1 ml - ivermax pour-on (ivermectin topical solution) applied at the recommended dose level of 500 mcg/kg is indicated for the effective control of these parasites. gastrointestinal roundworms mites sarcoptes scabiei var. bovis lice linognathus vituli haematopinus eurysternus damalinia bovis solenopotes capillatus horn flies haematobia irritans

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boehringer ingelheim animal health usa inc. - ivermectin (unii: 8883yp2r6d) (ivermectin - unii:8883yp2r6d), pyrantel pamoate (unii: 81bk194z5m) (pyrantel - unii:4qih0n49e7) - for use in dogs to prevent canine heartworm disease by eliminating the tissue stage of heartworm larvae (dirofilaria immitis ) for a month (30 days) after infection and for the treatment and control of roundworms (toxocara canis , toxascaris leonina ) and hookworms (ancylostoma caninum , uncinaria stenocephala , ancylostoma braziliense ).