Dextrose 5%/nacl 0.3% Inj, 250ml

Manufacturer FRESENIUS KABI USA Active Ingredient Intravenous (IV) Fluids(in truh VEE nuhs FLOO ids) Pronunciation DEK-strohs five per-SENT / NAY-see-el point three per-SENT IN-jek-shun
It is used to give fluids to the body when more fluids and electrolytes are needed.It is used as a way to give other drugs as a shot.It may be given to you for other reasons. Talk with the doctor.
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Drug Class
Fluid, Electrolyte, and Nutrient Replenisher
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Pharmacologic Class
Crystalloid Solution; Carbohydrate
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Pregnancy Category
Category C
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FDA Approved
Jan 1970
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DEA Schedule
Not Controlled

Overview

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What is this medicine?

This medicine is a sterile solution given through a vein (IV) to provide your body with water, a small amount of salt (sodium chloride), and a little sugar (dextrose) for energy. It helps keep your body's fluids and electrolytes balanced, especially when you can't drink enough or need extra hydration and a few calories.
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How to Use This Medicine

Proper Use of This Medication

To use this medication correctly, follow your doctor's instructions and read all the information provided. This medication is administered as an infusion into a vein over a period of time. Your doctor may instruct you on how to self-administer this medication.

Before and after handling the medication, wash your hands thoroughly. Do not use the medication if the solution appears cloudy, is leaking, or contains particles. Additionally, do not use the solution if it has changed color.

To dispose of used needles and other sharp objects, use a needle/sharp disposal box. Never reuse needles or other items. When the disposal box is full, follow local regulations for proper disposal. If you have any questions or concerns, consult your doctor or pharmacist.

Storage and Disposal

Typically, this medication is administered in a hospital or doctor's office. If you need to store it at home, follow the storage instructions provided by your doctor.

Missed Dose

If you miss a dose, contact your doctor to determine the best course of action.
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Lifestyle & Tips

  • Report any unusual symptoms or discomfort during the infusion.
  • Maintain good oral hygiene if unable to eat or drink normally.
  • Follow any dietary or fluid restrictions recommended by your healthcare provider.

Dosing & Administration

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Adult Dosing

Standard Dose: Highly individualized based on patient's fluid, electrolyte, and caloric needs, clinical condition, and body weight. Typical infusion rates vary from 40-125 mL/hour.
Dose Range: 40 - 125 mg

Condition-Specific Dosing:

dehydration: Higher rates initially, then adjusted based on response.
maintenance: Lower rates for ongoing fluid and electrolyte balance.
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Pediatric Dosing

Neonatal: Highly individualized based on weight (e.g., 60-100 mL/kg/day), fluid status, and electrolyte needs. Close monitoring essential.
Infant: Highly individualized based on weight (e.g., 80-120 mL/kg/day), fluid status, and electrolyte needs. Close monitoring essential.
Child: Highly individualized based on weight (e.g., 60-100 mL/kg/day), fluid status, and electrolyte needs. Close monitoring essential.
Adolescent: Highly individualized based on weight (e.g., 40-80 mL/kg/day), fluid status, and electrolyte needs. Close monitoring essential.
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Dose Adjustments

Renal Impairment:

Mild: Use with caution; monitor fluid balance and electrolytes closely.
Moderate: Use with caution; monitor fluid balance and electrolytes closely. May require reduced infusion rates to prevent fluid overload.
Severe: Contraindicated in severe renal failure with oliguria/anuria unless fluid removal methods (e.g., dialysis) are in place. Close monitoring of fluid balance, electrolytes, and glucose is critical.
Dialysis: May be used to provide fluid and calories, but careful consideration of fluid volume and electrolyte content is necessary to avoid overload or imbalances between dialysis sessions.

Hepatic Impairment:

Mild: No specific adjustment required, but monitor fluid balance.
Moderate: No specific adjustment required, but monitor fluid balance closely due to increased risk of fluid retention and ascites.
Severe: No specific adjustment for the drug itself, but extreme caution is needed due to increased risk of fluid retention, ascites, and electrolyte disturbances. Monitor fluid balance and electrolytes meticulously.

Pharmacology

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Mechanism of Action

Dextrose provides a source of calories and free water. It is metabolized via glycolysis and the Krebs cycle, producing carbon dioxide and water. Sodium chloride provides essential electrolytes (sodium and chloride) which are crucial for maintaining fluid and electrolyte balance, osmotic pressure, and normal cellular function. The solution helps to expand extracellular fluid volume and provides a small amount of calories.
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Pharmacokinetics

Absorption:

Bioavailability: 100%
Tmax: Not applicable (immediate distribution)
FoodEffect: Not applicable

Distribution:

Vd: Dextrose distributes throughout total body water; Sodium and Chloride distribute primarily throughout the extracellular fluid.
ProteinBinding: None (Dextrose); Minimal (Sodium, Chloride)
CnssPenetration: Yes (water, glucose, and electrolytes cross the blood-brain barrier)

Elimination:

HalfLife: Not a typical pharmacokinetic parameter for these components; elimination is continuous based on metabolic demand and renal excretion.
Clearance: Dextrose is cleared metabolically; Sodium and Chloride are primarily cleared renally.
ExcretionRoute: Renal (water, sodium, chloride); Respiratory (carbon dioxide from dextrose metabolism)
Unchanged: Sodium and chloride are excreted largely unchanged; Dextrose is metabolized.
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Pharmacodynamics

OnsetOfAction: Immediate
PeakEffect: Immediate
DurationOfAction: Dependent on infusion rate, patient's metabolic rate, and renal function. Effects are sustained as long as infusion continues.

Safety & Warnings

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Side Effects

Urgent Side Effects: Seek Medical Help Right Away

Although rare, some people may experience severe and potentially life-threatening side effects while taking this medication. If you notice any of the following symptoms, contact your doctor immediately or seek emergency medical attention:

Signs of an allergic reaction, such as:
+ Rash
+ Hives
+ Itching
+ Red, swollen, blistered, or peeling skin with or without fever
+ Wheezing
+ Tightness in the chest or throat
+ Trouble breathing, swallowing, or talking
+ Unusual hoarseness
+ Swelling of the mouth, face, lips, tongue, or throat
Signs of fluid and electrolyte problems, such as:
+ Mood changes
+ Confusion
+ Muscle pain or weakness
+ Fast or abnormal heartbeat
+ Severe dizziness or passing out
+ Increased thirst
+ Seizures
+ Feeling very tired or weak
+ Decreased appetite
+ Unable to pass urine or change in the amount of urine produced
+ Dry mouth
+ Dry eyes
+ Severe upset stomach or vomiting
Signs of skin infection, such as:
+ Oozing
+ Heat
+ Swelling
+ Redness
+ Pain
Swelling, warmth, numbness, change of color, or pain in a leg or arm
Chest pain or pressure
Fever
Shortness of breath
Sudden weight gain
Swelling in the arms or legs

Other Possible Side Effects

Like all medications, this drug can cause side effects. Many people may not experience any side effects or may only have mild ones. If you notice any of the following side effects or any other unusual symptoms, contact your doctor for advice:

Irritation or swelling at the injection site
* Pain at the injection site

This is not a comprehensive list of all possible side effects. If you have questions or concerns about side effects, consult your doctor. You can also report side effects to the FDA at 1-800-332-1088 or online at https://www.fda.gov/medwatch.
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Seek Immediate Medical Attention If You Experience:

  • Swelling in your hands, feet, or ankles
  • Difficulty breathing or shortness of breath
  • Unusual thirst or dry mouth
  • Confusion or dizziness
  • Muscle weakness or cramps
  • Irregular or fast heartbeat
  • Excessive urination or very little urination
  • Pain, redness, or swelling at the IV site
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Before Using This Medicine

Before Taking This Medication: Important Information to Share with Your Doctor

It is essential to inform your doctor about any allergies you have, including:
- An allergy to this medication or any of its components
- An allergy to other medications, foods, or substances
When discussing your allergies, be sure to describe the symptoms you experienced.

This medication may interact with other medications or health conditions. To ensure safe use, it is crucial to:
- Inform your doctor and pharmacist about all the medications you are taking, including prescription and over-the-counter drugs, natural products, and vitamins
- Share information about any health problems you have
You must verify that it is safe to take this medication with all your other medications and health conditions. Never start, stop, or change the dose of any medication without first consulting your doctor.
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Precautions & Cautions

It is essential to inform all your healthcare providers, including doctors, nurses, pharmacists, and dentists, that you are taking this medication.

If your medication contains potassium, consult your doctor before using any salt substitutes or products that also contain potassium.

If your medication contains dextrose and you have diabetes (high blood sugar), discuss this with your doctor to ensure safe management of your condition.

Regular blood tests will be necessary as directed by your doctor. Be sure to follow their instructions and discuss any concerns or questions you may have.

When administering this medication to newborns, exercise caution, as they may have a higher risk of experiencing side effects.

If you are pregnant, planning to become pregnant, or are breastfeeding, inform your doctor. They will help you weigh the benefits and risks of this medication to both you and your baby, ensuring you make an informed decision about your care.
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Overdose Information

Overdose Symptoms:

  • Fluid overload (e.g., pulmonary edema, peripheral edema, hypertension)
  • Hypernatremia (e.g., thirst, lethargy, confusion, seizures, coma)
  • Hyperglycemia (e.g., polyuria, polydipsia, fatigue, blurred vision, osmotic diuresis)
  • Electrolyte imbalances (e.g., hyperchloremia, hypokalemia due to dilution)

What to Do:

If you suspect an overdose, immediately notify your healthcare provider. Management involves discontinuing the infusion, administering diuretics to remove excess fluid, and correcting any severe electrolyte or glucose imbalances. In severe cases, dialysis may be required. Call 911 or poison control (1-800-222-1222) for immediate medical advice.

Drug Interactions

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Contraindicated Interactions

  • Patients with known hypersensitivity to corn or corn products (for dextrose)
  • Patients with clinically significant hypernatremia or hyperchloremia
  • Patients with severe hyperglycemia or uncontrolled diabetes mellitus
  • Patients with anuria or severe oliguria (unless dialysis is initiated)
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Major Interactions

  • Corticosteroids (may increase sodium and fluid retention)
  • Drugs that cause sodium retention (e.g., NSAIDs, some antihypertensives)
  • Drugs that affect glucose metabolism (e.g., insulin, oral hypoglycemics - may require dose adjustment)
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Moderate Interactions

  • Diuretics (especially loop diuretics - may alter electrolyte balance, requiring careful monitoring)
  • Drugs that increase ADH secretion (e.g., carbamazepine, oxcarbazepine, SSRIs, tricyclic antidepressants - may increase risk of hyponatremia)

Monitoring

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Baseline Monitoring

Serum Electrolytes (Na, K, Cl)

Rationale: To establish baseline fluid and electrolyte status and identify pre-existing imbalances.

Timing: Prior to initiation of therapy

Blood Glucose

Rationale: To assess baseline glucose levels, especially in diabetic or critically ill patients.

Timing: Prior to initiation of therapy

Renal Function (BUN, Creatinine)

Rationale: To assess kidney's ability to excrete fluid and electrolytes.

Timing: Prior to initiation of therapy

Fluid Status (Weight, Vital Signs, I&O)

Rationale: To assess hydration status and identify signs of fluid overload or dehydration.

Timing: Prior to initiation of therapy

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Routine Monitoring

Serum Electrolytes (Na, K, Cl)

Frequency: Every 12-24 hours, or more frequently as clinically indicated (e.g., every 4-6 hours in critical care)

Target: Na: 135-145 mEq/L; K: 3.5-5.0 mEq/L; Cl: 98-106 mEq/L

Action Threshold: Values outside normal range, especially trending towards hypernatremia, hyponatremia, or hypokalemia.

Blood Glucose

Frequency: Every 4-6 hours, or as clinically indicated, especially in diabetic or stressed patients.

Target: 70-180 mg/dL (individualized)

Action Threshold: Persistent hyperglycemia (>180 mg/dL) or hypoglycemia (<70 mg/dL).

Fluid Balance (Intake & Output, Daily Weight)

Frequency: Every 8-24 hours, or more frequently in critically ill patients.

Target: Balanced I&O, stable weight (or desired change)

Action Threshold: Significant positive or negative fluid balance, rapid weight gain/loss, signs of fluid overload or dehydration.

Vital Signs (BP, HR, RR)

Frequency: Every 4-8 hours, or as clinically indicated.

Target: Within patient's normal limits

Action Threshold: Changes indicative of fluid overload (e.g., elevated BP, crackles) or dehydration (e.g., orthostatic hypotension, tachycardia).

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Symptom Monitoring

  • Signs of fluid overload (e.g., peripheral edema, pulmonary crackles, dyspnea, elevated jugular venous pressure)
  • Signs of dehydration (e.g., dry mucous membranes, decreased skin turgor, decreased urine output, thirst)
  • Symptoms of electrolyte imbalance (e.g., muscle weakness, cramps, confusion, lethargy, seizures, cardiac arrhythmias)
  • Symptoms of hyperglycemia (e.g., polyuria, polydipsia, fatigue, blurred vision)
  • Symptoms of hypoglycemia (e.g., sweating, tremors, dizziness, confusion, hunger)

Special Patient Groups

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Pregnancy

Generally considered safe and often used for hydration and electrolyte balance during pregnancy. Close monitoring of fluid and electrolyte status is recommended.

Trimester-Specific Risks:

First Trimester: No specific risks identified.
Second Trimester: No specific risks identified.
Third Trimester: No specific risks identified. Can be used for hydration during labor and delivery.
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Lactation

Compatible with breastfeeding. The components (water, glucose, sodium, chloride) are natural constituents of breast milk and are not expected to cause adverse effects in the infant.

Infant Risk: Low risk.
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Pediatric Use

Dosing must be carefully calculated based on weight, age, and clinical condition to avoid fluid overload, electrolyte imbalances (especially hyponatremia), and hyperglycemia. Close monitoring of fluid balance, electrolytes, and glucose is critical.

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Geriatric Use

Increased susceptibility to fluid overload, electrolyte imbalances (e.g., hyponatremia, hypernatremia), and renal impairment. Requires careful monitoring of fluid balance, electrolytes, and renal function. Lower infusion rates may be necessary.

Clinical Information

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Clinical Pearls

  • This solution is hypotonic relative to plasma after dextrose metabolism, providing free water. It is useful for maintenance fluid therapy and to replace insensible fluid losses.
  • Always monitor serum electrolytes (especially sodium) and blood glucose levels closely, particularly in patients at risk for hyponatremia (e.g., SIADH, post-operative patients) or hyperglycemia (e.g., diabetics, stressed patients).
  • Not suitable for rapid volume expansion alone due to its hypotonicity after dextrose metabolism.
  • Not a significant source of calories for prolonged nutritional support; other solutions or methods are needed for full nutritional requirements.
  • Administer slowly to avoid rapid fluid shifts and potential complications like cerebral edema (in susceptible patients) or osmotic diuresis.
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Alternative Therapies

  • Oral Rehydration Solutions (for mild to moderate dehydration)
  • Other intravenous crystalloid solutions (e.g., Plasma-Lyte, Normosol-R)
  • Colloid solutions (e.g., albumin, for specific volume expansion needs)
  • Parenteral nutrition (for comprehensive nutritional support)
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Cost & Coverage

Generic Available: Yes
Insurance Coverage: Tier 1 (Preferred Generic)
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General Drug Facts

If your symptoms or health problems persist or worsen, it is essential to contact your doctor promptly. To ensure safe use, never share your medication with others or take someone else's medication. Store all medications in a secure location, out of reach of children and pets, to prevent accidental ingestion. Dispose of unused or expired medications properly; do not flush them down the toilet or pour them down the drain unless instructed to do so by a healthcare professional. If you are unsure about the correct disposal method, consult your pharmacist, who can also inform you about potential drug take-back programs in your area. Additionally, some medications may come with a separate patient information leaflet, which your pharmacist can provide. If you have any questions or concerns about your medication, discuss them with your doctor, nurse, pharmacist, or other healthcare provider. In the event of a suspected overdose, immediately contact your local poison control center or seek emergency medical attention. Be prepared to provide information about the medication taken, the amount, and the time it occurred.