Proper usage of drugs, chemicals and feed additives in food animals
Proper Usage of Drugs, Chemicals and Feed Additives in Show Market Animals Floron (Buddy) C. Faries, Jr., DVM, MS
Texas A&M AgriLife Extension Service
Definition of a Drug: Based on Usage
Any compound administered or applied with the intent: Approved Drug Types
Vaccines Antibiotics/Antibacterials Chemicals Hormones/Steroids
Food Animal Residue Avoidance Databank Within-Label Drug Usage
Approved drug for animal species on label Correct route on label Correct dosage on label Usage on label Withdrawal time on label
Drug Withdrawal Time
Drug elimination time for safe level in body
Drug below tolerant level in tissues
Time more than 24 hrs – not considered safe
Total drug elimination time longer than WT
Do not enter show until WT and ET expired
Drug in urine Urine must be drug negative
Drug above tolerant level in tissues
Drug Elimination Time
Time to be eliminated from body Do not enter show until expired
Time more than 24 hrs – considered safe
Prescription Drugs
Caution: Federal law restricts this drug to
use by or on the order of a licensed veterinarian
Unapproved Drug Types
Tranquilizers (ace, thorazine) Natural tranquilizers (vitamin B6, tryptophan, herbs) Local anesthetics (procaine, lidocaine) Diuretics (except Lasix®, Diuril® for udder edema) Natural dewormers (tobacco, garlic, DE) Caffeine diuretics (coffee, tea, chocolate, soda) Alcohol tranquilizers (beer, whiskey) Human drugs (topical, oral, parenteral)
Prohibited Drug Types
Diethylsilbestrol Chloramphenicol Nitroimidazoles Clenbuterol Dipyrone Fluoroquinolines Glycopeptides Nitrofurans (oral, topical, parenteral) Gentian Violet Sulfonamide (adult dairy cattle) Phenylbutazone (adult dairy cattle)
Extra-Label Drug Usage Approved animal drugs and human drugs
Federal law restricts extra-label drug use by or on the order
Dispensed: Veterinarian Label Prescribed: Veterinarian Prescription Not permitted in feed and water
Ractopamines (Paylean®, Optaflexx®, Topmax®)
The Houston Livestock Show™ will not be testing for the presence of
zilpaterol hydrochloride (Showmaxx®) in market steers.
Additionally, the Show will not be testing for the presence of
ractopamine hydrochloride in market steers (Optaflexx™), market
barrows (Paylean®), or market turkeys (Topmax™).
Exhibitors who choose to use these products are expected to follow all
label directions, including any published withdrawal times.
The Show will not tolerate the presence of zilpaterol hydrochloride or
ractopamine hydrochloride in species or classes within species for which they are not FDA approved.
The use of all other drugs, both unapproved and FDA approved, will be
governed by the Junior Show Rules published in the Exhibitor Handbook.
Medicated Feed Coccidiostats Goats Medicated Feed Antibacterials Antibiotics Dewormers Approved Drugs for Rabbits
No medicated feed antibacterials No antibiotics No dewormers
References
Use of Preventative and Therapeutic Drugs in Show
Proper Usage of Drugs and Chemicals in Food
Proper Use of Sulfonamides in Market Show Animals
LIQUAMYCIN LA-200® (OXYTETRACYCLINE INJECTION) Each ml contains 200mg of oxytetracycline base as oxytetracycline amphoteric For Use in Beef Cattle, Nonlactating Dairy Cattle and Swine
injection) is a sterile, ready-to-use solution
refrigeration; however, it is recommended
for the administration of the broad-spectrum
that it be stored at room temperature, 15°-
antibiotic oxytetracycline (Terramycin) by
30°C (59°-86°F). The antibiotic activity of
injection. Terramycin, discovered by Pfizer
scientists, is an antimicrobial agent that is
diminished in the presence of body fluids,
effective in the treatment of a wide range of
Discontinue treatment at least 28 days prior LIQUAMYCIN® LA-200 ® administered to to slaughter of cattle and swine. cattle or swine for the treatment of bacterial pneumonia at an intramuscular dosage of 9 milligrams of oxytetracycline per pound of body weight, has been demonstrated in clinical trials to be as effective as two or three repeated, daily treatments of Terramycin ® Injectable at 3 to 5 milligrams per pound of body weight. PRECAUTIONS
Exceeding the highest recommended dosage level of drug per pound of body weight per day, administering more than the recommended number of treatments, and/or exceeding 10 ml intramuscularly per injection site in adult beef cattle and nonlactating dairy cattle, and 5 ml intramuscularly per injection site in adult swine, may result in antibiotic residues beyond the withdrawal period. Reactions of an allergic or anaphylactic nature, sometimes fatal, have been known to occur in hypersensitive
animals following the injection of oxytetracycline. Such adverse reactions can be characterized by signs such as restlessness, erection of hair, muscle trembling; swelling of eyelids, ears, muzzle, anus and vulva ( or scrotum and sheath in males); labored breathing, defecation and urination, glassy-eyed appearance, eruption of skin plaques, frothing from the mouth, and prostration. Pregnant animals that recover may subsequently abort. At the first sign of any adverse reaction, discontinue use of this product and administer epinephrine at the recommended dosage levels. Call a veterinarian immediately.
Shock may be observed following intravenous administration, especially where highly concentrated materials
are involved. To minimize this occurrence, it is recommended that LIQUAMYCIN® LA-200 ® be administered slowly by this route.
Shortly after injection, treated animals may have transient hemoglobinuria resulting in darkened urine. As with all antibiotic preparations, use of this drug may result in overgrowth of non-susceptible organisms,
including fungi. A lack or response by the treated animal, or the development of new signs, may suggest that an overgrowth of non-susceptible organisms has occurred. If any of these conditions occur, consult your veterinarian.
Since bacteriostatic drugs may interfere with the bactericidal action of penicillin, it is advisable to avoid giving
LIQUAMYCIN® LA-200 ® in conjunction with penicillin.
STORAGE: Store at room temperature, 15°-30°C (59°-86°F). Keep from freezing. Lasix® (furosemide) A diuretic-saluretic for prompt relief of
Lasix ® (furosemide), a diuretic, is an anthranilic
acid derivative with the following structural
Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian. DESCRIPTION
Lasix ® (furosemide) is a chemically distinct
diuretic and saluretic pharmacodynamically characterized by the following:
1) A high degree of efficacy, low-inherent
3) A pharmacological action in the functional
area of the nephron, i.e., proximal and distal
tubules and the ascending limb of the loop
4) A dose-response relationship and a ratio of minimum to maximum effective dose
Generic name: Furosemide (except in United
Kingdom-frusemide). Chemical name: 4-chloro-N-furfuryl-5-sulfamoylanthranilic acid.
5) If may be administered orally or parenterally. It is readily absorbed from the
intestinal tract and well tolerated. The
intravenous route produces the most rapid diuretic response.
INDICATIONS Dogs Cats & Horses
(furosemide) is from the activity of the
range. Pharmacologically it promotes the
extracellular fluids. The rationale for the
a result of the drug's rapid absorption
producing the edema. Lasix® furosemide)
excretion minimize the possibility of its
associated with cardiac insufficiency and
crystalluria. Lasix® (furosemide) has no
inhibitory effect on carbonic anhydrase or
aldosterone activity in the distal tubule.
The drug possesses diuretic activity either
in presence of acidosis or alkalosis 1,2,3,4,5,6,7
DOSAGE ORAL Lasix ® (furosemide) is indicated for the DOG AND CAT treatment of physiological parturient
One-half to one 5O mg scored tablet per 25
edema of the mammary gland and associated
pounds body weight. One 12.5 mg tablet per 5
structures.
to 10 pounds body weight. Administer once or
twice daily permitting a 6- to 8-hour interval
CONTRAINDICATIONS - PRECAUTIONS
between treatments. In refractory or severe
Lasix ® (furosemide) is a highly effective
edematous cases the dosage may be doubled or
diuretic-saluretic which it given in excessive
increased by increments of 1 mg per pound body
electrolyte imbalance Therefore, the dosage and
paragraphs “Dosage and Administration“
patient's needs. The animal should be observed
PARENTERAL:
for early signs of electrolyte imbalance and
DOG AND CAT
corrective measures administered. Early signs
Administer intramuscularly or Intravenously 1/4
of eleclrolyte imbalance are increased thirst,
lethargy, drowsiness or restlessness fatigue,
Administer once or twice daily, permitting a 6- to
oliguria, gastro-intestinal disturbances and
8-hour interval between treatments. In refractory
tachycardia. Special attention should be given to
or severe edematous cases the dosage may be
potassium levels. Lasix ® (furosemide) may
doubled or increased by increments of 1 mg per
lower serum calcium levels and cause tetany in
rare cases of animals having an existing
HOW SUPPLIED
The individual dose is 250 to 500 mg (5 to
Parental: Lasix ® (furosemide) injection
intravenously once or twice daily at 6- to 8-
hour intervals until desired results are
stabilized with myristyl-gamma-picolinium
evaluate the degree of edema present and
adjust dosage schedule accordingly. Do
sodium sulfite 0.1% with sodium chloride
not use in horses intended for food.
0.2% in distilled water pH adjusted with
Tablets:
intramuscularly or intravenously is 500 mg
twice daily at 12-hour intervals. Treatment
4-chloro-N-furfuryl-5-sulfamoylanthranilic
not be used for food. Cattle must not be
4-chloro-N-furfuryl-5-sulfamoylanthranilic
slaughtered for food within 48 hours following last treatment. CAUTION. Federal law restricts this drug to use by or on the order of a licensed veterinarian DESCRIPTION
Acepromazine Maleate, a potent neuroleptic agent with a
low order of toxicity, is of particular value In the
tranquilization of dogs, cats, and horses. Its rapid action
and lack of hypnotic effect are added advantages.
According to Baker,' the scope of possible applications
for this compound in veterinary practice is only limited by
CHEMISTRY
Acepromazine (10.(3.(dimethylamino) propyl)
phenothiazin-2-yl-methyl ketonel Maleate has the
ACTIONS:
depressant effect on the central nervous
system and therefore causes sedation, muscular
PromAce Injectable can be used as an aid in
relaxation and a reduction in spontaneous
activity It acts rapidly, exerting a prompt and
transportation. Particularly useful when
used in conjunction with local anesthesia for
INDICATIONS:
firing, castration, neurectomy, removal of
DOGS AND CATS
skin tumors, ocular surgery and applying casts.
PromAce Injectable and Tablets can be used as
an aid in controlling intractable animals during
examination, treatment. grooming, x.ray, and
minor surgical procedures; to alleviate itching as a result of skin irritation; as an antie-metic to control vomiting associated with motion sickness. PromAce Injectable is particularly useful as a preanesthetic agent (1) to enhance and prolong the effects of barbiturates, thus reducing the requirements for general anesthesia; (2) as an adjunct to surgery under Local anesthesia.
Case report Clin Ter 2013; 164 (3):e207-209. doi: 10.7417/CT.2013.1570 A case of sensitization to Alitretinoin T. Grieco, V. Faina, L. Dies, M. Milana, L. Alei, E. Silvestri, S. Calvieri Department of Dermatology, “Sapienza” University of Rome, Italy Abstract Case report Alitretinoin is a unique retinoid authorised for the treatment of adults with severe chronic hand eczem
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