Description:
(GENTAMICIN
SULFATE WITH BETAMETHASONE VALERATE)
Veterinary
For Topical Use
in Dogs Only
ANADA #200-188,
Approved by FDA.
CAUTION:
Federal law restricts this drug to use by or on the order of a licensed
veterinarian.
DESCRIPTION:
Each mL contains: gentamicin sulfate equivalent to 0.57 mg gentamicin base,
betamethasone valerate equivalent to 0.284 mg betamethasone, 163 mg isopropyl
alcohol, propylene glycol, methylparaben and propylparaben as preservatives,
purified water q.s. Hydrochloric acid may be added to adjust pH.
CHEMISTRY:
Gentamicin is a mixture of aminoglycoside antibiotics derived from the
fermentation of Micromonospora purpurea. Gentamicin sulfate is a
mixture of sulfate salts of the antibiotics produced in this fermentation. The
salts are weakly acidic and freely soluble in water.
Gentamicin sulfate
contains not less than 500 micrograms of gentamicin base per milligram.
Betamethasone
valerate is a synthetic glucocorticoid.
PHARMACOLOGY:
Gentamicin, a broad-spectrum antibiotic, is a highly effective topical
treatment for bacterial infections of the skin. In vitro, gentamicin is
bactericidal against a wide variety of gram-positive and gram-negative
bacteria isolated from domestic animals.1,2 Specifically,
gentamicin is active against the following organisms isolated from canine
skin: Alcaligenes sp., Citrobacter sp., Klebsiella sp.,
Pseudomonas aeruginosa, indole-positive and negative Proteus sp,
Escherichia coli, Enterobacter sp., Staphylococcus sp.,
and Streptococcus sp.
Betamethasone
valerate emerged from intensive research as the most promising of some 50
newly synthesized corticosteroids in the experimental model described by
McKenzie3, et al. This human bioassay technique has been
found reliable for evaluating the vasoconstrictor properties of new topical
corticosteroids and is useful in predicting clinical efficacy.
Betamethasone
valerate in veterinary medicine has been shown to provide anti-inflammatory
and antipruritic activity in the topical management of corticosteroid
responsive infected superficial lesions in dogs.
WARNING:
Clinical and experimental data have demonstrated that corticosteroids
administered orally or parenterally to animals may induce the first stage of
parturition when administered during the last trimester of pregnancy and may
precipitate premature parturition followed by dystocia, fetal death, retained
placenta, and metritis.
Additionally,
corticosteroids administered to dogs, rabbits and rodents during pregnancy
have produced cleft palate. Other congenital anomalies including deformed
forelegs, phocomelia, and anasarca have been reported in offspring of dogs
which received corticosteroids during pregnancy.
INDICATIONS:
For the treatment of infected superficial lesions in dogs caused by bacteria
sensitive to gentamicin.
CONTRAINDICATIONS:
If hypersensitivity to any of the
components occurs, treatment with this product should be discontinued and
appropriate therapy instituted.
DOSAGE AND
ADMINISTRATION: Prior to
treatment, remove excessive hair and clean the lesion and adjacent area. Hold
bottle upright 3 to 6 inches from the lesion and depress the sprayer head
twice. Administer 2 to 4 times daily for 7 days.
Each depression of
the sprayer head delivers 0.7 mL of GentaVed Topical Spray.
TOXICITY:
Gentamicin sulfate with betamethasone valerate topical spray was well
tolerated in an abraded skin study in dogs. No treatment-related toxicological
changes in the skin were observed.
Systemic effects
directly related to treatment were confined to histological changes in the
adrenals, liver, and kidney and to organ-to-body weight ratios of adrenals.
All were dose related, were typical for or not unexpected with corticosteroid
therapy, and were considered reversible with cessation of treatment.
SIDE EFFECTS:
Side effects such as SAP and SGPT enzyme elevations, weight loss, anorexia,
polydipsia, and polyuria have occurred following parenteral or systemic use of
synthetic corticosteroids in dogs. Vomiting and diarrhea (occasionally bloody)
have been observed in dogs.
Cushings syndrome in
dogs has been reported in association with prolonged or repeated steroid
therapy.
PRECAUTIONS:
Antibiotic susceptibility of the pathogenic organism(s) should be determined
prior to the use of this preparation. Use of topical antibiotics may permit
overgrowth of non-susceptible bacteria, fungi, or yeasts. If this occurs,
treatment should be instituted with other appropriate agents as indicated.
Administration of
recommended dose beyond 7 days may result in delayed wound healing. Animals
treated longer than 7 days should be monitored closely.
Avoid ingestion.
Oral or parenteral use of corticosteroids, depending on dose, duration, and
specific steroid may result in inhibition of endogenous steroid production
following drug withdrawal.
In patients
presently receiving or recently withdrawn from systemic corticosteroid
treatments, therapy with a rapidly acting corticosteroid should be considered
in especially stressful situations.
If ingestion should
occur, patients should be closely observed for the usual signs of
adrenocorticoid overdosage which include sodium retention, potassium loss,
fluid retention, weight gains, polydipsia, and/or polyuria. Prolonged use or
overdosage may produce adverse immunosuppressive effects.
HOW SUPPLIED:
Plastic spray bottle containing 60 mL, 120 mL or 240 mL of GentaVed Topical
Spray.
Store upright
between 2°C and 30°C (36°F and 86°F).
Manufactured for
VEDCO, Inc. St.
Joseph, MO 64504
|
Net Contents: |
NDC |
|
60 mL. |
50989-461-19 |
|
120 mL. |
50989-461-74 |
|
240 mL. |
50989-461-75 |
|