Примери за използване на Caused by mycoplasma spp на Английски и техните преводи на Български
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Respiratory tract Infections caused by Mycoplasma spp.
Infections caused by Mycoplasma spp(Micoplasmosis, CRD) or Pasteurella multocida(Pasteurellosis).
Infections of the respiratory tract caused by Mycoplasma spp., Escherichia coli.
The efficacy data do not support the use of tylosin for the treatment of bovine mastitis caused by Mycoplasma spp.
Respiratory infections caused by Mycoplasma spp., E. coli and Haemophilus paragallinarum.
Delete, where applicable,the indication‘bovine mastitis caused by Mycoplasma spp.'.
For the treatment of respiratory infections caused by Mycoplasma spp., E. coli, Haemophilus paragallinarum, Bordetella avium, and ileitis caused by Clostridium perfringens and Cl. colinum.
Delete, where applicable,any references to‘bovine mastitis caused by Mycoplasma spp.
Infections of the respiratory tract caused by Mycoplasma spp., Escherichia coli, Haemophilus paragallinarum and Bordetella avium;- Enteritis caused by Clostridium perfringens and Clostridium colinum.
The CVMP was requested to review all available data andto provide its opinion on whether the indication related to'bovine mastitis caused by Mycoplasma spp.'.
Why were veterinary medicinal products containing tylosin that are administered parenterally andintended for the treatment of bovine mastitis caused by Mycoplasma spp.
The Agency's Committee for Medicinal Products for Veterinary Use(CVMP) concluded that, in the absence of pre-clinical orclinical data, treatment of bovine mastitis caused by Mycoplasma spp.
However, it is difficult, if not impossible, to assess the true level of lack of efficacy of tylosin in the treatment of‘bovine mastitis caused by Mycoplasma spp.'.
Overall summary of the scientific evaluation of veterinary medicinal products containing tylosin that are administered parenterally andintended for the treatment of bovine mastitis caused by Mycoplasma spp.
Finland noted that there are veterinary medicinal products containing tylosin thatare administered parenterally and intended for the treatment of bovine mastitis caused by Mycoplasma spp.
In the absence of pre-clinical orclinical data and in light of the current scientific knowledge the CVMP considered that the treatment of bovine mastitis caused by Mycoplasma spp.
The CVMP has recommended the variation of the marketing authorisations for veterinary medicinal products containing tylosin thatare administered parenterally and intended for the treatment of bovine mastitis caused by Mycoplasma spp.
In this procedure none of the concerned applicants/marketing authorisation holders provided data in support of the use of parenterally administered tylosin in the treatment of bovine mastitis caused by Mycoplasma spp.
No pre-clinical or clinical data in support of the indication were provided from theapplicants/marketing authorisation holders and no benefits of the use on tylosin in treatment of mastitis caused by Mycoplasma spp.
On 16 March 2017, the European Medicines Agency(the Agency) completed a review of the effectiveness of veterinary medicinal products containing tylosin that are administered parenterally andintended for the treatment of bovine mastitis caused by Mycoplasma spp.
On 22 June 2016, Finland initiated a referral procedure under Article 35 of Directive 2001/82/EC, for veterinary medicinal products containing tylosin that are administered parenterally andintended for the treatment of bovine mastitis caused by Mycoplasma spp.
The aim of the referral procedure was to consider the available data andcurrent scientific knowledge regarding the efficacy of parenterally administered tylosin formulations authorised for the treatment of bovine mastitis caused by Mycoplasma spp.
The Committee recommended variations to the terms of the marketing authorisations for the aforementioned veterinary medicinal products in order to remove the indications‘bovine mastitis caused by Mycoplasma spp.'.
The Committee for Medicinal Products for Veterinary Use(CVMP) was requested to consider the available data andthe current scientific knowledge, and to provide its opinion on whether the indication'bovine mastitis caused by Mycoplasma spp.'.
Based on the evaluation of the currently-available data, the CVMP concluded that, in the absence of specific pre-clinical orclinical data, and in light of the current scientific knowledge, the indication for treatment of bovine mastitis caused by Mycoplasma spp.
Some field data were presented to support use of the product in the treatment of pneumonia caused by Mycoplasma and P. haemolytica in calves, but there were no clinical or field data to support use of the product in the treatment of pleuropneumonia(H. somni) or bronchopneumonia involving H. somni, P. multocida, Streptococcus spp or A. pyogenes.
Treatment of infections of the respiratory tract caused by enrofloxacin susceptible strains of: Pasteurella multocida, Mycoplasma spp., Actinobacillus pleuropneumoniae.
Treatment of infections of the respiratory tract caused by enrofloxacin susceptible strains of Pasteurella multocida, Mannheimia haemolytica and Mycoplasma spp.
Treatment of infections of the respiratory tract caused by enrofloxacin susceptible strains of Actinobacillus pleuropneumoniae, Pasteurella multocida and Mycoplasma spp.
Bronchopneumonia and pleuropneumonia caused by Pasteurella spp., Streptococcus spp., Arcanobacterium pyogenes, Histophilus somni and Mycoplasma spp.