VetStarch ™6% HYDROXYETHYL STARCH 130/0.4 IN 0.9% SODIUM CHLORIDE INJECTION For Animal Use Only CAUTION: Federal Law (USA) restricts this drug to use by or on the order of a licensed veterinarian.

VETSTARCH- hydroxyethyl starch 130/0.4 injection, solution 
Abbott Laboratories

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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CLINICAL PHARMACOLOGY

Mechanism of Action

VetStarch contains hydroxyethyl starch in a colloidal solution which expands plasma volume when administered intravenously. This effect depends on the mean molecular weight (130,000 daltons; range 110,000 – 150,000 daltons), the molar substitution by hydroxyethyl groups (0.4; range 0.38 – 0.45) on glucose units of the starch, the pattern of hydroxyethyl substitution (C2/C6 ratio) of approximately 9:1, and the concentration (6%), as well as the dosage and infusion rate.

Hydroxyethyl starch is a derivative of thin boiling waxy corn starch, which mainly consists of a glucose polymer (amylopectin) predominately composed of a-1-4-connected glucose units with several a-1-6-branches. Substitution of hydroxyethyl groups on the glucose units of the polymer reduces the normal degradation of amylopectin by a-amylase in the body. The low molar substitution (0.4) is the main pharmacological determinant for the beneficial effects of VetStarch on pharmacokinetics, intravascular volume and hemodilution.6 To describe the molecular weight and molar substitution characteristics of the hydroxyethyl starch in VetStarch, the compound is designated as hydroxyethyl starch 130/0.4.

INDICATIONS AND USAGE

VetStarch™ (6% hydroxyethyl starch 130/0.4 in 0.9% sodium chloride injection) is indicated for the treatment and prophylaxis of hypovolemia. It is not a substitute for red blood cells or coagulation factors in plasma.

CONTRAINDICATIONS

The use of VetStarch™ is contraindicated in the following conditions:

• Known hypersensitivity to hydroxyethyl starch [see General Warnings and Precautions]

• Fluid overload (hyperhydration) and especially in cases of pulmonary edema and congestive heart failure

• Renal failure with oliguria or anuria not related to hypovolemia

• Patients receiving dialysis treatment

• Severe hypernatremia or severe hyperchloremia

• Intracranial bleeding

WARNINGS AND PRECAUTIONS

General Warnings and Precautions

Anaphylactoid reactions (bradycardia, tachycardia, bronchospasm, non-cardiac pulmonary edema) have been reported with solutions containing hydroxyethyl starch.3 If a hypersensitivity reaction occurs, administration of the drug should be discontinued immediately and the appropriate treatment and supportive measures should be undertaken until symptoms have resolved. [see Adverse Reactions]

Fluid status and rate of infusion should be assessed regularly during treatment, especially in patients with cardiacinsufficiency or severe kidney dysfunction.

In cases of severe dehydration, a crystalloid solution should be given first. Generally, sufficient fluid should be administered in order to avoid dehydration.

Caution should be observed before administering VetStarch to patients with severe liver disease or severe bleeding disorders. With the administration of certain hydroxyethyl starch solutions, disturbances of blood coagulation can occur depending on the dosage.4,5

Monitoring: Laboratory Tests

Clinical evaluation and periodic laboratory determinations are necessary to monitor fluid balance, electrolyte concentrations, kidney function, acid-base balance, and coagulation parameters during prolonged parenteral therapy, or whenever the patient’s condition warrants such evaluation.

Interference with Laboratory Tests

In humans, elevated serum amylase levels may be observed temporarily following administration of the product and can interfere with the diagnosis of pancreatitis.

At high dosages the dilutional effects may result in decreased levels of coagulation factors and other plasma proteins and a decrease in hematocrit.4,5

DRUG INTERACTIONS

No interactions with other drugs or nutritional products are known. The safety and compatibility of other additives have not been established.4,5 [see Directions for Use of VetStarch]

ADVERSE REACTIONS

Overall Adverse Reaction Profile

Products containing hydroxyethyl starch may lead to anaphylactoid reactions (hypersensitivity, mild influenza-like symptoms, bradycardia, tachycardia, bronchospasm, non-cardiac pulmonary edema). In the event of an intolerance reaction, the infusion should be discontinued immediately and the appropriate emergency medical treatment initiated. [see General Warnings and Precautions]

Skin and subcutaneous tissue disorders in humans; prolonged administration of high dosages of hydroxyethyl starch may cause pruritus (itching) which is an undesirable effect observed with all hydroxyethyl starches.

Investigations; at high doses, the dilutional effects may result in decreased levels of coagulation factors and other plasma proteins, and a decrease in hematocrit. [see Interference with Laboratory Tests]

DESCRIPTION

VetStarch™ (6% hydroxyethyl starch 130/0.4 in 0.9% sodium chloride injection) is a clear to slightly opalescent, colorless to slightly yellow, sterile, non-pyrogenic, isotonic solution for intravenous administration using sterile equipment.

Each 100 mL of the solution contains:

Hydroxyethyl Starch 130/0.4 6 g
Sodium Chloride USP in Water for Injection USP 900 mg
pH adjusted with Sodium Hydroxide USP or Hydrochloric Acid USP

Electrolytes (mEq/L): Sodium 154, Chloride 154, pH 4 to 5.5. Calculated osmolarity 308 mOsmol/L. The hydroxyethyl starch contained in VetStarch is a synthetic colloid for use in plasma volume replacement. The chemical name of hydroxyethyl starch is poly(O-2-hydroxyethyl) starch. The structural formula of hydroxyethyl starch is:

chemicalstructure

VetStarch is packaged in 250 mL and 500 mL flexible plastic containers made from coextruded polyolefin and is free of PVC,plasticizers, adhesives or latex (Non-DEHP, Latex-free). The container offers an air-closed system and can be used with nonvented IV sets which prevent external air contamination. The container is collapsible and can be used in emergency cases for pressure infusion.

OVERDOSAGE

As with all plasma volume substitutes, overdosage can lead to overloading of the circulatory system (e.g., pulmonary edema). In this case, the infusion should be stopped immediately and, if necessary, a diuretic should be administered. [see General Warnings and Precautions]

DOSAGE AND ADMINISTRATION

VetStarch is administered by intravenous infusion only. The daily dose and rate of infusion depend on the patient’s blood loss, on the maintenance or restoration of hemodynamics and on the hemodilution (dilution effect). VetStarch can be administered repetitively over several days. [see Warnings and Precautions] The initial 10 to 20 mL should be infused slowly, keeping the patient under close observation due to possible anaphylactoid reactions. [see General Warnings and Precautions]

Adult Dose

As a general recommendation, the class of synthetic colloids are prescribed at doses up to 20 mL per kg of body weight per day in small animal patients.1 In a 30 kg patient, this is a dose of 600 mL of VetStarch (equivalent to 1.2 g hydroxyethyl starch and 3.1 mEq sodium per kg of body weight). The use of 6% hydroxyethyl starch 130/0.4 has been dosed at 50 mL per kg of body weight per day in human studies.2

Directions for Use of VetStarch

directionsforuse

1. Do not remove the IV container from its overwrap until immediately before use.

2. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.

3. Do not administer unless the solution is clear, free from particles and the IV container is undamaged.

4. VetStarch should be used immediately after insertion of the administration set.

5. Do not vent.

6. If administered by pressure infusion, air should be withdrawn or expelled from the bag through the medication/administration port prior to infusion.

7. Discontinue the infusion if an adverse reaction occurs.

8. It is recommended that administration sets be changed at least once every 24 hours.

9. For single use only. Discard unused portion.

INCOMPATIBILITIES

The safety and compatibility of additives have not been established.

DOSAGE FORMS AND STRENGTHS

250 mL and 500 mL flexible plastic intravenous solution containers are available. Each 100 mL contains 6 g hydroxyethyl starch 130/0.4 in isotonic sodium chloride injection.

NONCLINICAL TOXICOLOGY

Carcinogenesis, Mutagenesis, Impairment of Fertility

Long-term studies in animals, to evaluate the carcinogenic potential of VetStarch, have not been performed. No mutagenic effects were observed with hydroxyethyl starch 130/0.4 10% solution in the following tests on mutagenic activity: Salmonella typhimurium reverse mutation assay (in vitro), mammalian cells in the in vitro gene mutation assay, assessment of the clastogenic activity in cultured human peripheral lymphocytes (in vitro), bone marrow cytogenetic test in Sprague-Dawley rats.

Fertility studies on directly exposed animals have not been performed.

Animal Toxicology and Pharmacology

Toxicology

Three-month repeat infusion toxicology studies were conducted in rats and dogs in which three groups of animals were administered daily intravenous infusion over three hours. Dosing volumes of either 60 or 90 mL/kg body weight of hydroxyethyl starch 130/0.4 (10% solution), or 90 mL/kg 0.9% sodium chloride injection, were studied. Observed toxicity following repeat infusion of hydroxyethyl starch is consistent with the oncotic properties of the solution resulting in hypervolemia in the animals.

There were no apparent gender-related effects on toxicity following repeat administration of hydroxyethyl starch 130/0.4 in rats or dogs.

In reproduction studies in rats and rabbits, hydroxyethyl starch 130/0.4 (10% solution) had no teratogenic properties. Embryolethal effects were observed in rabbits at 5 g/kg body weight/day. In rats, bolus injection of this dose during pregnancy and lactation reduced body weight of offspring and induced developmental delays. Signs of fluid overload were seen in the dams. Hydroxyethyl starch 130/0.4 (10% solution) was observed to have no effect in studies assessing skin sensitization, antigenicity, and blood compatibility.

PHARMACOLOGY

The pharmacodynamic effect of VetStarchTM was examined in a hemorrhagic shock model in conscious rats, and a hemodilution model in dogs. In both studies, the control group received pentastarch (6% hydroxyethyl starch 200/0.5).

VetStarch was as effective as pentastarch in maintaining cardiopulmonary function during isovolemic hemodilution in beagle dogs. In the three-hour follow-up period, no additional administration of colloid was necessary.

There were no differences in long-term survival of rats after a single administration of VetStarch and pentastarch solutions following induced hemorrhagic shock (67% and 50% blood loss). In the 67% induced bleeding group receiving VetStarch (N=6), the survival rate was 83% which is within the normal range for this type of experiment. In the corresponding pentastarch group, survival was 100%. Infusion of Ringer’s lactate resulted in a 50% survival rate after a 50% blood loss and a 0% survival after a 67% blood loss. After multiple intravenous infusions of 0.7 g per kg body weight per day of 10% hydroxyethyl starch 130/0.4, or 10% hydroxyethyl starch 200/0.5 solution, during 18 consecutive days, the plasma hydroxyethyl starch concentration in rats treated with hydroxyethyl starch 130/0.4 was lower compared to rats treated with hydroxyethyl starch 200/0.5. Hydroxyethyl starch 130/0.4 was eliminated faster than hydroxyethyl starch 200/0.5. In both groups, clear signs of hydroxyethyl starch tissue storage were detected in lymph nodes and spleen. Numerous empty vacuoles in macrophages were observed. Only minimal cellular vacuolization was found in the liver and kidney. Histochemical differences between the groups were not observed.

A study with 10% radiolabeled 14C-hydroxyethyl starch 130/0.4 and 10% 14C-hydroxyethyl starch 200/0.5 solutions was carried out.7 In animals treated with hydroxyethyl starch 130/0.4, radioactivity decreased from 4.3% of the total administered dose (2.6 g hydroxyethyl starch 130/0.4 per animal) on day 3 to 0.65% on day 52. In animals treated with hydroxyethyl starch 200/0.5, the 14C activity decreased from 7.7% of the total administered dose (2.7 g hydroxyethyl starch 200/0.5 per animal) on day 3 to 2.45% on day 52. These results confirm the faster elimination and lower persistence of hydroxyethyl starch 130/0.4 in tissue.

USE IN SPECIFIC POPULATIONS

Pregnancy

The type of hydroxyethyl starch present in VetStarch had no teratogenic properties in rats or rabbits. At 5 g/kg of body weight per day, administered as a bolus injection, fetal retardations and embryolethal effects were observed in rats and rabbits, respectively. In rats, a bolus injection of this dose during pregnancy and lactation reduced body weight of offspring and induced developmental delays. All adverse effects were seen exclusively at maternal toxic doses due to fluid overload. [see Toxicology]

Fertility studies on directly exposed animals have not been conducted.

Labor and Delivery

Information on the use of VetStarch during labor or delivery is unknown.

Renal Impairment

VetStarch is mainly excreted by the kidneys, and the risk of adverse reactions to this drug may be greater in patients with impaired renal function. Volume status, infusion rate, and urine output should be closely monitored.

REFERENCES

1. Silverstein D, Hopper K. Small Animal Critical Care Medicine. (2009).

2. Neff T., Doelberg M., Jungheinrich C., Sauerland A., Spahn D., Stocker R., “Repetitive Large-Dose Infusion of the Novel Hydroxyethyl Starch 130/0.4 in Patients with Severe Head Injury.” Anesth Analg 96 (2003): 1453-9

3. DiBartola, S. Fluid, Electrolyte, & Acid-Base Disorders in Small Animal Practice. (2011).

4. Smiley, et al. “The Use of Hetastarch as Adjunct Therapy in 36 dogs with Hypoalbuminemia: a Phase Two Clinical Trial.”J Vet Intern Med, 8 (1994): 195-200.

5. Smart, et al. “The Effect of Hetastarch (670/0.75) In Vivo on Platelet Closure Time in the Dog.” J Vet Emerg Crit Care, 19(5) (2009): 444-449.

6. Jungheinrich, C., Neff, T. “Pharmacokinetics of hydroxyethyl starch.” Clin Pharmacokinetik 44 (7) (2005): 681-699.

7. Leuschner, J., Opitz, J., Winkler, A., Scharpf, R., Bepperling, F. “Tissue storage of 14C-labeled hydroxyethyl starch (HES) 130/0.4 and HES 200/0.5 after repeated intravenous administration to rats.” Drugs R D, 4 (6) (2003): 331-8.

HOW SUPPLIED

VetStarch™ (6% hydroxyethyl starch 130/0.4 in 0.9% sodium chloride injection) for intravenous infusion is supplied in the following primary container and carton sizes:

Polyolefin bag with overwrap: 250 mL and 500 mL

Carton of 20 x 500 mL

Carton of 30 x 250 mL

Store at 15° to 25°C (59° to 77°F), Do not freeze

For Customer Service call (888) 299-7416

Manufactured for:

Abbott Laboratories

1401 N. Sheridan Road,

North Chicago, IL 60064 USA

Product of Norway

PRINCIPAL DISPLAY PANEL

250mlbag
500mlbag
VETSTARCH 
hydroxyethyl starch (130/0.4 substitution) injection, solution
Product Information
Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:0074-4950
Route of AdministrationINTRAVENOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROXYETHYL STARCH 130/0.4 (HYDROXYETHYL STARCH 130/0.4) HYDROXYETHYL STARCH 130/0.46000 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE900 mg  in 100 mL
SODIUM HYDROXIDE 
HYDROCHLORIC ACID 
Packaging
#Item CodePackage Description
1NDC:0074-4950-03250 mL in 1 BAG
2NDC:0074-4950-05500 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other10/12/201204/16/2013
Labeler - Abbott Laboratories (078458370)
Registrant - Abbott Laboratories (001307602)
Establishment
NameAddressID/FEIBusiness Operations
Fresenius Kabi Austria GmbH303448575api manufacture

Revised: 04/2013
 
Abbott Laboratories