new YORK (Reuters) – A federal judge ordered to the
U.S. regulators to withdraw the authorization of use
of common antibiotics in feedingstuffs, the mention
concern that excessive use can put in
risk human health by creating “superbacterias” resistant to
medication.
The judge Theodore Katz ordered Thursday the Administration
food and United States drugs (FDA by its acronym
in English) to begin procedures to put an end to the
authorization unless the producers of medicines
can generate evidence that their use is safe.
If the laboratories can not prove that inofensividad,
the FDA must withdraw approval for non-medical uses of
these drugs, the judge ruled.
The Agency had begun with these procedures in 1997,
driven by concerns about the widespread use in the
food for the cattle of certain antibiotics, particularly
tetracycline and penicillin, more common. But that process never
was completed and the authorization remains in effect.
“in these years has been growing scientific evidence of the
“
risks to the health of the expanded of antibiotics use
in cattle, and there is no evidence that the FDA has changed its
position on that isn’t shown that these uses are
“
insurance”, wrote Katz.
The demand was made by environmental groups and
defence of public health.
The plaintiffs argued that use common antibiotics
in the cattle feed contributed to rapid growth
of bacteria resistant to drugs in animals as
human.
Antibiotic-resistant infections cost to the
Americans over 20 billion dollars annually,
the plaintiffs, who cited a 2009 study indicated
the Alliance for the prudent use of antibiotics and Hospital
the Cook County.
In his letter, Katz ordered the FDA move forward with the process
initiated in 1977 but only formally abandoned in December
passed. The FDA said that the procedures were
out-of-date and which purported to follow other strategies
regulatory to deal with problems of security
food.
“the FDA has not issued any statement since the launch
“
(the news) in 1977 that undermines the original findings of that
“
drugs have not proven to be safe”, wrote Katz.
The FDA could not be immediately contacted to carry out
comments in this regard.