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940 Comments
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tcsgroupq
4:24 AM on February 25, 2022
(dectomax) is a veterinary drug approved by the food and drug administration (fda) for the treatment of parasites such as gastrointestinal roundworms, lungworms, eyeworms, grubs, sucking lice and mange mites in cattle.
it is used for the treatment and control of internal parasitosis (gastrointestinal and pulmonary nematodes), ticks and mange (and other ectoparasites). doramectin is a derivative of ivermectin. similarly to other drugs of this family, it is produced by fermentation by selected strains of streptomyces avermitilis. its spectrum includes: haemonchus, ostertagia, trichostrongylus, cooperia, and oesophagostomum species and dictyocaulus viviparus, dermatobia hominis, boophilus microplus, and psoroptes bovis, among many other internal and external parasites. it is available as an injection and as a 5-mg/ml topical solution.
doramectin is also marketed in many latin-american and some asia and africa countries as doramec l.a. (manufactured by agrovet market animal health) in a 1% doramectin long acting injectable solution for cattle, sheep, swine and others. its oleous carrier confers to doramec l.a. a slow and prolonged liberation, extending its action up to 42 days.
doramectin is also available for horses as an oral, flavored, bioadhesive gel under the name doraquest l.a. oral gel. it can be used to control and treat internal parasites as roundworms, lungworms and some external parasites.
it is used for the treatment and control of internal parasitosis (gastrointestinal and pulmonary nematodes), ticks and mange (and other ectoparasites). doramectin is a derivative of ivermectin. similarly to other drugs of this family, it is produced by fermentation by selected strains of streptomyces avermitilis. its spectrum includes: haemonchus, ostertagia, trichostrongylus, cooperia, and oesophagostomum species and dictyocaulus viviparus, dermatobia hominis, boophilus microplus, and psoroptes bovis, among many other internal and external parasites. it is available as an injection and as a 5-mg/ml topical solution.
doramectin is also marketed in many latin-american and some asia and africa countries as doramec l.a. (manufactured by agrovet market animal health) in a 1% doramectin long acting injectable solution for cattle, sheep, swine and others. its oleous carrier confers to doramec l.a. a slow and prolonged liberation, extending its action up to 42 days.
doramectin is also available for horses as an oral, flavored, bioadhesive gel under the name doraquest l.a. oral gel. it can be used to control and treat internal parasites as roundworms, lungworms and some external parasites.
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tcsindustryr
3:26 PM on February 28, 2022
cidofovir, brand name vistide, is an injectable antiviral medication primarily used as a treatment for cytomegalovirus (cmv) retinitis (an infection of the retina of the eye) in people with aids.
cidofovir was approved for medical use in 1996.
medical use
dna virus
its only indication that has received regulatory approval worldwide is cytomegalovirus retinitis. cidofovir has also shown efficacy in the treatment of aciclovir-resistant hsv infections. cidofovir has also been investigated as a treatment for progressive multifocal leukoencephalopathy with successful case reports of its use. despite this, the drug failed to demonstrate any efficacy in controlled studies. cidofovir might have anti-smallpox efficacy and might be used on a limited basis in the event of a bioterror incident involving smallpox cases. brincidofovir, a cidofovir derivative with much higher activity against smallpox that can be taken orally has been developed. it has inhibitory effects on varicella-zoster virus replication in vitro although no clinical trials have been done to date, likely due to the abundance of safer alternatives such as aciclovir. cidofovir shows anti-bk virus activity in a subgroup of transplant recipients. cidofovir is being investigated as a complementary intralesional therapy against papillomatosis caused by hpv.
it first received fda approval on 26 june 1996, tga approval on 30 april 1998 and ema approval on 23 april 1997.
it has been used topically to treat warts.
cidofovir was approved for medical use in 1996.
medical use
dna virus
its only indication that has received regulatory approval worldwide is cytomegalovirus retinitis. cidofovir has also shown efficacy in the treatment of aciclovir-resistant hsv infections. cidofovir has also been investigated as a treatment for progressive multifocal leukoencephalopathy with successful case reports of its use. despite this, the drug failed to demonstrate any efficacy in controlled studies. cidofovir might have anti-smallpox efficacy and might be used on a limited basis in the event of a bioterror incident involving smallpox cases. brincidofovir, a cidofovir derivative with much higher activity against smallpox that can be taken orally has been developed. it has inhibitory effects on varicella-zoster virus replication in vitro although no clinical trials have been done to date, likely due to the abundance of safer alternatives such as aciclovir. cidofovir shows anti-bk virus activity in a subgroup of transplant recipients. cidofovir is being investigated as a complementary intralesional therapy against papillomatosis caused by hpv.
it first received fda approval on 26 june 1996, tga approval on 30 april 1998 and ema approval on 23 april 1997.
it has been used topically to treat warts.
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tcsindustryn
6:08 AM on April 11, 2022
micafungin, sold under the brand name mycamine, is a polyene antifungal medication used to treat and prevent invasive fungal infections including candidemia, abscesses and esophageal candidiasis. it inhibits the production of beta-1,3-glucan, an essential component of fungal cell walls. micafungin is administered intravenously. it received final approval from the u.s. food and drug administration (fda) on march 16, 2005, and gained approval in the european union on april 25, 2008.
indications
micafungin is indicated for the treatment of candidemia, acute disseminated candidiasis, candida peritonitis, abscesses and esophageal candidiasis. since january 23, 2008, micafungin has been approved for the prophylaxis of candida infections in patients undergoing hematopoietic stem cell transplantation (hsct).
micafungin works by way of concentration-dependent inhibition of 1,3-beta-d-glucan synthase resulting in reduced formation of 1,3-beta-d-glucan, which is an essential polysaccharide comprising one-third of the majority of candida spp. cell walls. this decreased glucan production leads to osmotic instability and thus cellular lysis.
indications
micafungin is indicated for the treatment of candidemia, acute disseminated candidiasis, candida peritonitis, abscesses and esophageal candidiasis. since january 23, 2008, micafungin has been approved for the prophylaxis of candida infections in patients undergoing hematopoietic stem cell transplantation (hsct).
micafungin works by way of concentration-dependent inhibition of 1,3-beta-d-glucan synthase resulting in reduced formation of 1,3-beta-d-glucan, which is an essential polysaccharide comprising one-third of the majority of candida spp. cell walls. this decreased glucan production leads to osmotic instability and thus cellular lysis.
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