Farhan
Ali
DVM 6th Semester
Faculty of veterinary
Sciences Multan
: BZU
Human Safety of Veterinary Drug Residues
“Residues of Veterinary Drugs
include the parent compounds or their metabolites in any edible portion of the
animal product and include the residues of associated impurities of the
Veterinary drug concerned“.
Food animals convert one source
of Nutrional energy (grass , hay , grain ) into another (meat ,milk
,eggs ) .Food animal production practice requires management of animal health
and this can require the use of drug .Human health and this can require the use
of drug .Human health effects of food animal drugs can arise from drug
residues.
Food producing species
|
Energy product
|
Consumes per capita(pound)
|
cattle
|
Meat
|
110
|
cows
|
Fish
|
16.1
|
chickens
|
Poultry
|
73.6
|
Goat
|
Egg
|
32.7
|
Camel
|
Dairy product
|
600.5
|
To determine
residual effect of Veterinary drugs (Antibiotics , Antiparasitic ,bactericides,
fungicides etc ). Drug sponsor conducts a standard battery of toxicological
test .This battery includes studies that examine the effect of the product on
systemic toxicity, mutagenicity , reproductive ,and developmental toxicity . The
toxicological studies are designed to identify a dose that cause a toxic effect
and a dose that cause no observed Effect . This no observed effect level is
divided by a safety factor to calculate an Acceptable Daily Intake (ADI) of
drug residues. The ADI represent the amount of drug residues that can be safety
consumed daily for as long as a lifetime .Once ADI is establish the drug sponsor
conduct drug metabolism and depletion studies .when the drug residues in target
tissue depletes below tolerance all edible tissue are considered safe for Human
consumption .These are special food safety concern for the residues of
veterinary drug .It is known that the therapeutics doses of these agents cause
adverse effect on Human intestinal micro flora . Drug Residues Testing by FAST
(fast antimicrobial screen test ), Lab test (HPLC), Target tissue tested Milk ,
kidney often tested at slaughter.
The Food and Drug administration is empowered with the
regulatory responsibility of ensuring that use of Veterinary drug in food animal does not result in adverse
heath consequences in Human. Before any animal drug may be Legally marketed and
drug sponsor must have a New Animal Drug
Application (NADA) approved by the FDA .
“Drug misuse is not a disease, it is a
decision, like the decision to step out in front of a moving car. You would
call that not a disease but an error of judgment.”
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