Dextrose 5%/nacl 0.45% Inj, 1000ml

Manufacturer BAXTER Active Ingredient Intravenous (IV) Fluids(in truh VEE nuhs FLOO ids) Pronunciation DEK-strose five per-SENT / NAY-klor-ide point four five 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 caloric replacement
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Pharmacologic Class
Crystalloid solution; Carbohydrate
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Pregnancy Category
Category C
FDA Approved
Jan 1970
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DEA Schedule
Not Controlled

Overview

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What is this medicine?

This medication is a sterile liquid given through a vein (intravenously). It contains a sugar (dextrose) for energy and salt (sodium chloride) to help balance your body's fluids and electrolytes. It's used to provide hydration, some calories, and replace lost salt and water when you can't take fluids by mouth or need extra support.
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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 solution if it 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 discomfort or pain at the IV site immediately.
  • Inform your healthcare provider if you experience swelling, difficulty breathing, or changes in urination.

Dosing & Administration

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Adult Dosing

Standard Dose: Individualized based on patient's fluid, electrolyte, and caloric needs. Typically 1000-3000 mL/24 hours, infused at a rate determined by clinical condition.

Condition-Specific Dosing:

dehydration: Rate adjusted to correct fluid deficit, typically 100-250 mL/hour.
maintenance: Rate adjusted to meet daily fluid and caloric requirements, typically 40-125 mL/hour.
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Pediatric Dosing

Neonatal: Individualized based on weight, age, and clinical condition. Typically 60-100 mL/kg/day, adjusted for fluid and electrolyte balance.
Infant: Individualized based on weight, age, and clinical condition. Typically 100-150 mL/kg/day, adjusted for fluid and electrolyte balance.
Child: Individualized based on weight, age, and clinical condition. Typically 1500 mL/m² BSA/day or 40-60 mL/kg/day, adjusted for fluid and electrolyte balance.
Adolescent: Individualized based on weight, age, and clinical condition. Similar to adult dosing, adjusted for fluid and electrolyte balance.
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Dose Adjustments

Renal Impairment:

Mild: Use with caution; monitor fluid and electrolyte balance closely.
Moderate: Use with caution; monitor fluid and electrolyte balance closely; may require reduced rates or volumes to prevent fluid overload.
Severe: Use with extreme caution; significant reduction in rate and volume often required; close monitoring of fluid balance, electrolytes, and renal function is critical.
Dialysis: Contraindicated or used with extreme caution and significant volume restriction, as fluid removal is managed by dialysis. Consult nephrology.

Hepatic Impairment:

Mild: No specific dose adjustment, but monitor for fluid retention.
Moderate: No specific dose adjustment, but monitor for fluid retention and electrolyte imbalances (e.g., hyponatremia).
Severe: No specific dose adjustment, but monitor closely for fluid retention, ascites, and electrolyte imbalances. May require fluid restriction.

Pharmacology

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Mechanism of Action

Dextrose 5% provides a source of calories (170 kcal/L) and free water, which is metabolized to carbon dioxide and water, helping to prevent ketosis and reduce protein catabolism. Sodium Chloride 0.45% (half-normal saline) provides sodium and chloride ions, essential electrolytes for maintaining fluid and electrolyte balance, and contributes to the tonicity of the solution, helping to expand the extracellular fluid compartment.
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Pharmacokinetics

Absorption:

Bioavailability: 100% (intravenous administration)
Tmax: Immediate (as infusion begins)
FoodEffect: Not applicable (IV administration)

Distribution:

Vd: Distributes throughout the total body water. Dextrose is rapidly distributed to tissues and cells. Sodium and chloride distribute primarily in the extracellular fluid.
ProteinBinding: Not applicable (electrolytes and simple sugar)
CnssPenetration: Yes (water, glucose, and electrolytes cross the blood-brain barrier)

Elimination:

HalfLife: Not applicable (continuously infused and utilized/excreted)
Clearance: Dextrose is cleared by cellular metabolism. Sodium and chloride are primarily cleared by renal excretion.
ExcretionRoute: Renal (water, sodium, chloride); Respiratory (CO2 from dextrose metabolism)
Unchanged: Not applicable (components are utilized or excreted)
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Pharmacodynamics

OnsetOfAction: Immediate (upon initiation of infusion)
PeakEffect: Continuous (effect maintained as long as infusion continues and components are utilized)
DurationOfAction: Dependent on infusion rate and patient's metabolic needs; effects cease shortly after discontinuation of infusion.

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 or seek immediate 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, including:
+ Mood changes
+ Confusion
+ Muscle pain or weakness
+ Fast or abnormal heartbeat
+ Severe dizziness or fainting
+ Increased thirst
+ Seizures
+ Feeling extremely tired or weak
+ Decreased appetite
+ Difficulty urinating or changes in urine output
+ Dry mouth
+ Dry eyes
+ Severe stomach upset or vomiting
Signs of skin infection, such as:
+ Oozing
+ Heat
+ Swelling
+ Redness
+ Pain
Swelling, warmth, numbness, color changes, 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. While many people may not experience any side effects or only minor ones, it's essential to discuss any concerns with your doctor. If you experience 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

Reporting Side Effects

This list is not exhaustive, and you may experience other side effects. If you have questions or concerns, don't hesitate to contact 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 (edema)
  • Shortness of breath or difficulty breathing
  • Rapid weight gain
  • Increased thirst or urination
  • Confusion or dizziness
  • Muscle weakness or cramps
  • 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 the following:

Any allergies you have, including allergies to this medication, its components, or other substances, such as foods or drugs. Be sure to describe the symptoms you experienced as a result of the allergy.
All medications you are currently taking, including prescription and over-the-counter (OTC) drugs, natural products, and vitamins. This information will help your doctor identify potential interactions between this medication and other substances.
* Any existing health problems, as this medication may interact with certain conditions.

To ensure your safety, it is crucial to verify that it is safe to take this medication with all your current medications and health conditions. Always consult your doctor before starting, stopping, or changing the dose of any medication.
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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 a salt substitute or any product that also contains potassium.

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

Regular blood tests will be necessary, as directed by your doctor, to monitor your condition. Be sure to follow your doctor's instructions and discuss any concerns with them.

When administering this medication to newborns, exercise caution, as the risk of side effects may be increased in this age group.

If you are pregnant, planning to become pregnant, or are breastfeeding, inform your doctor. It is crucial to discuss the potential benefits and risks of this medication to both you and your baby to make an informed decision.
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Overdose Information

Overdose Symptoms:

  • Fluid overload (e.g., pulmonary edema, peripheral edema, hypertension)
  • Electrolyte imbalances (e.g., hypernatremia, hypokalemia, hyperchloremia)
  • Hyperglycemia (high blood sugar)
  • Acidosis (due to excessive chloride or rapid infusion)

What to Do:

Immediate discontinuation of infusion, administration of diuretics (if fluid overload), correction of electrolyte imbalances, and insulin for hyperglycemia. Call 1-800-222-1222 (Poison Control) for specific guidance, though overdose is typically managed by the treating medical team.

Drug Interactions

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Major Interactions

  • Corticosteroids (may cause sodium and fluid retention)
  • Drugs causing sodium retention (e.g., NSAIDs, some antihypertensives)
  • Insulin (may require adjustment due to dextrose content)
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Moderate Interactions

  • Diuretics (may alter fluid and electrolyte balance, requiring careful monitoring)
  • Drugs affecting glucose metabolism (e.g., oral hypoglycemics)

Monitoring

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Baseline Monitoring

Serum Electrolytes (Na, K, Cl)

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

Timing: Prior to initiation of therapy

Blood Glucose

Rationale: To establish baseline glucose level, especially in diabetic patients or those at risk of hyperglycemia.

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, Edema)

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

Timing: Prior to initiation of therapy

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Routine Monitoring

Fluid Intake and Output (I&O)

Frequency: Every 4-8 hours or as clinically indicated

Target: Balanced I&O or as per fluid management goals

Action Threshold: Significant positive or negative fluid balance; signs of fluid overload or dehydration

Serum Electrolytes (Na, K, Cl)

Frequency: Daily or more frequently if clinically indicated (e.g., every 6-12 hours in critical patients)

Target: Sodium: 135-145 mEq/L; Potassium: 3.5-5.0 mEq/L; Chloride: 98-106 mEq/L

Action Threshold: Values outside normal range, especially hyponatremia or hypernatremia

Blood Glucose

Frequency: Every 4-6 hours initially, then daily once stable, or as per protocol for diabetic patients

Target: 70-180 mg/dL (individualized)

Action Threshold: Hypoglycemia (<70 mg/dL) or Hyperglycemia (>180 mg/dL)

Vital Signs (BP, HR, RR)

Frequency: Every 4-8 hours or as clinically indicated

Target: Within patient's normal limits

Action Threshold: Significant changes indicating fluid imbalance (e.g., hypotension, tachycardia, tachypnea)

Body Weight

Frequency: Daily

Target: Stable or as per fluid management goals

Action Threshold: Rapid weight gain (>1-2 kg/day) or loss

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Symptom Monitoring

  • Signs of fluid overload (e.g., peripheral edema, pulmonary crackles, dyspnea, jugular venous distension)
  • Signs of dehydration (e.g., dry mucous membranes, decreased skin turgor, decreased urine output, orthostatic hypotension)
  • Signs of electrolyte imbalance (e.g., muscle weakness, cramps, confusion, seizures, cardiac arrhythmias)
  • Signs of hyperglycemia (e.g., polyuria, polydipsia, fatigue, blurred vision)
  • Signs of phlebitis or extravasation at infusion site (pain, redness, swelling)

Special Patient Groups

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Pregnancy

Generally considered safe for use during pregnancy when clinically indicated for fluid and electrolyte replacement. Careful monitoring of fluid balance and electrolytes is important.

Trimester-Specific Risks:

First Trimester: No known specific risks, but use only if clearly needed.
Second Trimester: No known specific risks.
Third Trimester: No known specific risks, but monitor for fluid overload, especially in pre-eclamptic patients.
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Lactation

Considered safe for use during lactation. 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

Use with extreme caution in neonates and infants due to immature renal function and increased risk of fluid and electrolyte imbalances (e.g., hyponatremia, hyperglycemia). Close monitoring of fluid intake/output, electrolytes, and blood glucose is essential. Dosing is weight-based and highly individualized.

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Geriatric Use

Use with caution in elderly patients due to increased risk of fluid overload, electrolyte imbalances, and impaired renal or cardiac function. Start with lower infusion rates and monitor fluid status, electrolytes, and renal function closely.

Clinical Information

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Clinical Pearls

  • Always assess patient's fluid status, electrolyte levels, and renal function before initiating and throughout therapy.
  • Infusion rate must be carefully controlled to avoid fluid overload, especially in patients with cardiac, renal, or hepatic impairment.
  • Monitor blood glucose levels regularly, particularly in diabetic patients or those receiving prolonged infusions, to prevent hyperglycemia.
  • This solution is hypotonic relative to plasma (after dextrose metabolism) and can cause hyponatremia if administered rapidly or in large volumes, especially in pediatric patients or those with conditions predisposing to hyponatremia (e.g., SIADH).
  • Not suitable for rapid volume expansion alone; for significant hypovolemia, isotonic solutions (e.g., 0.9% NaCl) are generally preferred.
  • Check for particulate matter and discoloration before administration. Do not use if solution is not clear or seal is broken.
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Alternative Therapies

  • Oral rehydration solutions (for mild dehydration)
  • Other intravenous crystalloids or colloids depending on specific fluid and electrolyte needs
  • Parenteral nutrition (for comprehensive nutritional support)
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Cost & Coverage

Average Cost: $5 - $20 per 1000 mL bag
Generic Available: Yes
Insurance Coverage: Typically covered by most medical insurance plans as it is a standard hospital supply and medication.
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General Drug Facts

If your symptoms or health problems persist or worsen, it is essential to contact your doctor for further guidance. To ensure safe use, never share your medication with others, and do not take medication prescribed for someone else. 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. Unless instructed to do so by a healthcare professional, do not flush medications down the toilet or pour them down the drain. If you are unsure about the proper disposal method, consult your pharmacist for guidance. Many communities have drug take-back programs, which your pharmacist can help you locate. Some medications may come with an additional patient information leaflet; check with your pharmacist to see if this applies to your prescription. 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 was taken to ensure prompt and effective treatment.