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1.
Article in German | MEDLINE | ID: mdl-22167083

ABSTRACT

In 2010, three new active pharmaceutical ingredients were released on the German market for horses and food-producing animals. These were gamithromycin (Zactran®), a new macrolide antibiotic, Monepantel (Zolvix®), a broad spectrum anthelmintic with a novel mechanism, and Pergolide (Prascend®), the first dopamine receptor agonist for animals. Two substances have been approved for additional species. The tetracycline antibiotic doxycycline is now also authorized for turkeys and the nonsteroidal anti-inflammatory drug firocoxib from the group of cyclo-oxygenase-2 (COX-2) inhibitors is now available for horses. Furthermore, four new preparations with an interesting new pharmaceutical form, one drug with a new formulation and two drugs, which are interesting because of other criteria, were added to the market for horses and food producing animals.


Subject(s)
Animals, Domestic , Anthelmintics/standards , Anti-Bacterial Agents/standards , Cyclooxygenase 2 Inhibitors/standards , Dopamine Agonists/standards , Veterinary Drugs/standards , 4-Butyrolactone/analogs & derivatives , 4-Butyrolactone/standards , Aminoacetonitrile/analogs & derivatives , Aminoacetonitrile/standards , Animals , Cattle , Chickens , Doxycycline/standards , Germany , Horses , Macrolides/standards , Pergolide/standards , Sheep , Sulfones/standards , Swine , Turkeys
2.
N Z Vet J ; 57(4): 193-202, 2009 Aug.
Article in English | MEDLINE | ID: mdl-19649012

ABSTRACT

AIM: To demonstrate the clinical and reproductive safety in ewes and their offspring of repetitive oral doses of monepantel, an amino-acetonitrile derivative (AAD), when administered at three times the proposed maximum recommended dose (MRD) over an entire reproductive cycle. METHODS: A randomised controlled blinded study design was used. One hundred and twelve primi- or multi-parous ewes and 28 rams were randomly allocated into control and treated groups (n=56 for groups of ewes, n=14 for groups of rams). Two control ewes and two treated ewes were randomly selected to form 28 subgroups. A control or treated ram was then randomly allocated to each subgroup, to form control ram/treated ewe, control ram/control ewe, treated ram/treated ewe, and treated ram/control ewe 'treatment/mating' units. Control animals were treated with saline, and treated animals given three times the MRD (11.25 mg/kg) of monepantel. Treatments were administered orally every 5 days during an entire reproductive cycle, including oestrus and mating, gestation, and post-lambing to weaning. Detailed recording at multiple time points were made of veterinary examinations; observations for adverse events; bodyweight measurements; faecal scores; and haematology, clinical chemistry and coagulation variables. Reproductive indices determined included percent pregnant, number of failed embryos, abortion percentage, number of lambs with teratogenic defects, length of gestation, percentage of stillbirths, number of ewes experiencing reproductive problems, lambing percentage, and pre-weaning mortality. Post-mortem examination, including measurement of organ weights, was performed on randomly selected ewes (n=40) and lambs (n=40) at the completion of the study. RESULTS: All ewes treated with monepantel and those in the control group thrived and behaved normally to the end of the study. No treatment-related, toxicologically relevant adverse events, clinical observations or gross post-mortem changes were observed. Furthermore, there were no significant differences in bodyweight or organ weights, and haematological, clinical chemistry or coagulation variables between ewes treated with monepantel and control ewes. No significant differences were observed in any of the reproductive indices measured. No significant clinical differences were noted between lambs born from treated ewes and those from controls. CONCLUSIONS AND CLINICAL RELEVANCE: Repeated oral administration of monepantel at three times the MRD every 5 days over an entire reproductive cycle was not associated with any treatment-related adverse effects on the reproductive performance of ewes nor on the viability of their offspring, and was systemically very well tolerated. This study demonstrated that this population of ewes could tolerate accidental overdoses of up to three times the MRD of monepantel or prolonged repetitive administration of overdoses. Thus, those so treated entering a breeding programme would have normal reproductive indices, mating behaviour, and health, and their lambs would suffer no ill effects.


Subject(s)
Aminoacetonitrile/analogs & derivatives , Anthelmintics/administration & dosage , Pregnancy, Animal/drug effects , Reproduction/drug effects , Sheep/physiology , Administration, Oral , Aminoacetonitrile/administration & dosage , Aminoacetonitrile/standards , Aminoacetonitrile/toxicity , Analysis of Variance , Animals , Animals, Newborn , Anthelmintics/standards , Anthelmintics/toxicity , Autopsy/veterinary , Female , Male , Pregnancy , Sheep/blood
3.
Vet Rec ; 165(2): 50-2, 2009 Jul 11.
Article in English | MEDLINE | ID: mdl-19596676

ABSTRACT

Eighteen, six- to seven-month-old lambs were infected experimentally with larvae of Haemonchus contortus, Teladorsagia circumcincta, Trichostrongylus axei, Trichostrongylus colubriformis, Cooperia curticei and Nematodirus spathiger, and allocated to three equal groups. The infections were timed to ensure that fourth-stage larvae were present when groups 1 and 2 were treated orally with monepantel. Group 1 was not fed for 24 hours before the treatment, group 2 was fed two hours before the treatment and group 3 was fed at the same time as group 2 but not treated with monepantel. All the sheep had access to water. Worm burdens were determined 15 days after the treatments. Fasting or feeding had no statistically significant effects on the efficacy of the monepantel solution against the nematodes, and the period of fasting had no adverse effects.


Subject(s)
Aminoacetonitrile/analogs & derivatives , Antinematodal Agents/standards , Fasting , Sheep Diseases/drug therapy , Trichostrongyloidea/drug effects , Trichostrongyloidiasis/veterinary , Aminoacetonitrile/administration & dosage , Aminoacetonitrile/standards , Animals , Antinematodal Agents/administration & dosage , Disease Models, Animal , Euthanasia, Animal , Larva/drug effects , Parasitic Sensitivity Tests/methods , Parasitic Sensitivity Tests/veterinary , Sheep , Sheep Diseases/parasitology , Trichostrongyloidea/isolation & purification , Trichostrongyloidiasis/drug therapy
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