The introduction of additives to any solution, regardless of type of container, requires special attention to ensure that no incompatibilities result. While some incompatibilities are readily absorbed, one must be aware that subtle physical, chemical and pharmacological incompatibilities can occur. The medical literature, the package insert and other available sources of information should be reviewed for thorough understanding of possible incompatibilities.
GMS Electrolyte Solution Compound Sodium Lactate (Hartmann’s Solution) should be used with great care, if at all, in patients with congestive heart failure, severe renal insufficiency, and in clinical states in which there exists edema and sodium retention.
GMS Electrolyte Solution Compound Sodium Lactate (Hartmann’s Solution) should be used with great care, if at all, in patients with hyperkalemia, severe renal failure, and in conditions in which potassium retention is present.
GMS Electrolyte Solution Compound Sodium Lactate (Hartmann’s Solution) should be used with great care in patients with metabolic or respiratory alkalosis. The administration of lactate ions should be done with great care in those conditions in which there is an increased level or an impaired utilization of these ions, such as severe hepatic insufficiency.
GMS Electrolyte Solution Compound Sodium Lactate (Hartmann’s Solution) should not be administered simultaneously with blood through the same administration set because of likelihood of coagulation.
The intravenous administration of GMS Electrolyte Solution Compound Sodium Lactate (Hartmann’s Solution) can cause fluid and/or solute overloading resulting in dilution of serum electrolyte concentrations, over-hydration, congested states, or pulmonary edema. The risk of dilutional states is inversely proportional to the electrolyte concentrations of the injections. The risk of solute overloading causing congested states with peripheral and pulmonary edema is directly proportional to the electrolyte concentrations of the injections.
In patients with diminished renal function, administration of GMS Electrolyte Solution Compound Sodium Lactate (Hartmann’s Solution) may result in sodium or potassium retention.
Do not administer to horses by intraperitoneal injection. Do not administer to animals with inadequate renal function. Not for use in lactic acidosis.
GMS Electrolyte Solution Compound Sodium Lactate Hartmanns
Veterinary Lactated Ringer’s Injection, USP, should be used with great care, if at all, in patients with congestive heart failure, severe renal insufficiency, and in clinical states in which there exists edema with sodium retention.
Veterinary Lactated Ringer’s Injection, USP should be used with great care, if at all, in patients with hyperkalemia, severe renal failure, and in conditions in which potassium retention is present.
Veterinary Lactated Ringer’s Injection, USP should be used with great care in patients with metabolic or respiratory alkalosis. The administration of lactate ions should be done with great care in those conditions in which there is an increased level or an impaired utilization of these ions, such as severe hepatic insufficiency.
Veterinary Lactated Ringer’s Injection, USP should not be administered simultaneously with blood through the same administration set because of the likelihood of coagulation.
The container label for these injections bears the statement: Do not administer simultaneously with blood.
The intravenous administration of Veterinary Lactated Ringer’s Injection, USP can cause fluid and/or solute overloading resulting in dilution of serum electrolyte concentrations, over-hydration, congested states, or pulmonary edema.
The risk of dilutive states is inversely proportional to the electrolyte concentration of the injections.
The risk of solute overload causing congested states with peripheral and pulmonary edema is directly proportional to the electrolyte concentrations of the injections.
In patients with diminished renal function, administration of Veterinary Lactated Ringer’s Injection, USP may result in sodium retention proportional to the electrolyte concentrations of the injections.
Veterinary Lactated Ringer’s Injection, USP is not for use in the treatment of lactic acidosis
Keep out of the reach of children.
DailyMed 1eff6801-d00f-4430-a815-0a4720bb35d2
Do not administer to horses by intraperitoneal injection.
Veterinary Lactated Ringer's and 5% Dextrose Injection, USP should be used with great care, if at all, in patients with congestive heart failure, severe renal insufficiency, and in clinical states in which there exists edema with sodium retention.
Veterinary Lactated Ringer's and 5% Dextrose Injection, USP should be used with great care, if at all, in patients with hyperkalemia, severe renal failure, and in conditions in which potassium retention is present.
Veterinary Lactated Ringer's and 5% Dextrose Injection, USP should be used with great care in patients with metabolic or respiratory alkalosis. The administration of lactate ions should be done with great care in those conditions in which there is an increased level or an impaired utilization of these ions, such as severe hepatic insufficiency.
Veterinary Lactated Ringer's and 5% Dextrose Injection, USP should not be administered simultaneously with blood through the same administration set because of the likelihood of coagulation.
The intravenous administration of Veterinary Lactated Ringer's and 5% Dextrose Injection, USP can cause fluid and/or solute overloading resulting in dilution of serum electrolyte concentrations, overhydration, congested states, or pulmonary edema. The risk of dilutional states is inversely proportional to the electrolyte concentrations of the injections. The risk of solute overload causing congested states with peripheral and pulmonary edema is directly proportional to the electrolyte concentrations of the injection.
In patients with diminished renal function, administration of Veterinary Lactated Ringer's and 5% Dextrose Injection, USP may result in sodium or potassium retention.
Veterinary Lactated Ringer's and 5% Dextrose Injection, USP is not for use in the treatment of lactic acidosis.
Vetivex® Veterinary Lactated Ringer's and 5% Dextrose Injection, USP
COMPOUND SODIUM LACTATE (HARTMANN'S SOLUTION) Injection should be used with great care, if at all, in animals with congestive heart failure, severe renal insufficiency, and in clinical states in which there exists edema with sodium retention.
COMPOUND SODIUM LACTATE (HARTMANN'S SOLUTION) Injection should be used with great care, if at all, in animals with hyperkalemia, severe renal failure, and in conditions in which potassium retention is present.
COMPOUND SODIUM LACTATE (HARTMANN'S SOLUTION) Injection should be used with great care in animals with metabolic or respiratory alkalosis. The administration of lactate ions should be done with great care in those conditions in which there is an increased level or an impaired utilization of these ions, such as severe hepatic insufficiency.
COMPOUND SODIUM LACTATE (HARTMANN'S SOLUTION) Injection should not be administered simultaneously with blood through the same administration set because of the likelihood of coagulation.
The intravenous administration of COMPOUND SODIUM LACTATE (HARTMANN'S SOLUTION) Injection can cause fluid and/or solute overloading resulting in dilution of serum electrolyte concentrations, overhydration, congested states, or pulmonary edema. The risk of dilutional states is inversely proportional to the electrolyte concentrations of the injections. The risk of solute overload causing congested states with peripheral and pulmonary edema is directly proportional to the electrolyte concentrations of the injections.
In patients with diminished renal function, administration of COMPOUND SODIUM LACTATE (HARTMANN'S SOLUTION) Injection may result in sodium or potassium retention.
COMPOUND SODIUM LACTATE (HARTMANN'S SOLUTION) Injection is not for use in the treatment of lactic acidosis.
Electrolyte Solution COMPOUND SODIUM LACTATE (HARTMANN'S SOLUTION) 5 L
Lactated Ringer's and 5% Dextrose Injection, USP should be used with great care, if at all, in patients with congestive heart failure, severe renal insufficiency, and in clinical states in which there exists edema with sodium retention.
Lactated Ringer's and 5% Dextrose Injection, USP should be used with great care,if at all, in patients with hyperkalemia, severe renal failure, and in conditions in which potassium retention is present.
Lactated Ringer's and 5% Dextrose Injection, USP should be used with great care, in patients with metabolic or respiratory alkalosis. The administration of lactate ions should be done with great care in those conditions in which there is an increased level or an impaired utilization of these ions, such as severe hepatic insufficiency.
Lactated Ringer's and 5% Dextrose Injection, USP should not be administered simultaneously with blood through the same administration set because of the likelihood of coagulation
The intravenous administration of Lactated Ringer's and 5% Dextrose Injection, USP can cause fluid and/or solute overloading resulting in dilution of serum electrolyte concentrations, over hydration, congested states, or pulmonary edema. The risk of dilutive states is inversely proportional to the electrolyte concentration of the injections. The risk of solute overload causing congested states with peripheral and pulmonary edema is directly proportional to the electrolyte concentrations of the injections.
In patients with diminished renal function, administration of Lactated Ringer's and 5% Dextrose Injection, USP may result in sodium or potassium retention.
Lactated Ringer's and 5% Dextrose Injection, USP is not used for treatment of lactic acidosis.
Veterinary Lactated Ringer's and 5% Dextrose Injection, USP
Do not administer to horses by intraperitoneal injection.
Hartmann's Solution for Injection should be used with great care, if at all, in patients with congestive heart failure, severe renal insufficiency, and in clinical states in which there exists edema with sodium retention.
Hartmann's Solution for Injection should be used with great care, if at all, in patients with hyperkalemia, severe renal failure, and in conditions in which potassium retention is present.
Hartmann's Solution for Injection should be used with great care in patients with metabolic or respiratory alkalosis. The administration of lactate ions should be done with great care in those conditions in which there is an increased level or an impaired utilization of these ions, such as severe hepatic insufficiency.
Hartmann's Solution for Injection should not be administered simultaneously with blood through the same administration set because of the likelihood of coagulation.
The parenteral administration of Hartmann's Solution for Injection can cause fluid and/or solute overloading resulting in dilution of serum electrolyte concentrations, overhydration, congested states, or pulmonary edema. The risk of dilutional states is inversely proportional to the electrolyte concentrations of the injections. The risk of solute overload causing congested states with peripheral and pulmonary edema is directly proportional to the electrolyte concentrations of the injection.
In patients with diminished renal function, administration of Hartmann's Solution for Injection may result in sodium or potassium retention.
Hartmann's Solution for Injection is not for use in the treatment of lactic acidosis.
Vetivex® Hartmann's Solution for Injection
Do not administer to horses by intraperitoneal injection.
Lactated Ringer's Injection, USP should be used with great care, if at all, in patients with congestive heart failure, severe renal insufficiency, and in clinical states in which there exists edema with sodium retention.
Lactated Ringer's Injection, USP should be used with great care, if at all, in patients with hyperkalemia, severe renal failure, and in conditions in which potassium retention is present.
Lactated Ringer's Injection, USP should be used with great care, in patients with metabolic or respiratory alkalosis. The administration of lactate ions should be done with great care in those conditions in which there is an increased level or an impaired utilization of these ions, such as severe hepatic insufficiency.
Lactated Ringer's Injection, USP should not be administered simultaneously with blood through the same administration set because of the likelihood of coagulation
The intravenous administration of Lactated Ringer's Injection, USP can cause fluid and/or solute overloading resulting in dilution of serum electrolyte concentrations, over hydration, congested states, or pulmonary edema. The risk of dilutive states is inversely proportional to the electrolyte concentration of the injections. The risk of solute overload causing congested states with peripheral and pulmonary edema is directly proportional to the electrolyte concentrations of the injections.
In patients with diminished renal function, administration of lactated Ringer's Injection, USP may result in sodium or potassium retention.
Lactated Ringer's Injection, USP is not used for treatment of lactic acidosis.
Veterinary Lactated Ringer's Injection, USP
Clinical evaluation and periodic laboratory determinations are necessary to monitor changes in fluid balance, electrolyte concentrations, and acid base balance during prolonged parenteral therapy or whenever the condition of the animal warrants such evaluation.
COMPOUND SODIUM LACTATE (HARTMANN'S SOLUTION) Injection must be used with caution. Excess administration may result in metabolic alkalosis.
Caution must be exercised in the administration of COMPOUND SODIUM LACTATE (HARTMANN'S SOLUTION) Injection to patients receiving corticosteroids or corticotropin.
Do not administer unless solution is clear and seal is intact.
Reactions which may occur because of the solution or the technique of administration include febrile response, infection at the site of injection, venous thrombosis or phlebitis extending from the site of injection, extravasation, and hypervolemia.
If an adverse reaction does occur, discontinue the infusion, evaluate the animal, institute appropriate therapeutic countermeasures, and save the remainder of the fluid for examination if deemed necessary.
Electrolyte Solution COMPOUND SODIUM LACTATE (HARTMANN'S SOLUTION) 5 L
Avoid storage at cold temperatures which can cause product to become cloudy.
To clarify place product in warm water bath (100oF-120oF) for about 30 minutes.
KETO-PLEX FORTE
Do not administer to horses by intraperitoneal injection. Do not administer to animals with inadequate renal function. Not for use in lactic acidosis.
LACTATED RINGERS INJECTION
Shake well before use
Administer with care to avoid aspiration.
FOR ANIMAL USE ONLY
Milk Fever
TAKE TIME OBSERVE LABEL DIRECTIONS
KEEP OUT OF REACH OF CHILDREN
RX only.
Lactated Ringers
KEEP OUT OF
REACH OF CHILDREN
TAKE TIME OBSERVE LABEL DIRECTIONS
LACTATED RINGERS INJECTION
SHAKE WELL BEFORE USE
Administer with care to avoid aspiration.
Milk Fever
Do not administer to horses by intraperitoneal injection.
Lactated Ringers
TAKE TIME OBSERVE LABEL DIRECTIONS
ELECTROLYTE SOLUTION WITH DEXTROSE
KEEP OUT OF REACH OF CHILDREN
ELECTROLYTE SOLUTION WITH DEXTROSE