What is 5% w/v DEXTROSE INJECTION USP
5% w/v Dextrose Injection USP (2000ml Plastic Bag) is a sterile, non-pyrogenic intravenous solution composed of 5 grams of dextrose (glucose) per 100ml of water for injection. This results in a total of 100 grams of dextrose in a 2000ml bag. It is an isotonic solution widely used in hospitals and clinics to provide hydration, caloric supplementation, and as a vehicle for intravenous medication administration.
- Generic Name: Dextrose (Glucose)
- Concentration: 5% w/v (5g/100ml)
- Volume: 2000ml per plastic IV bag
- Osmolality: Approx. 252 mOsm/L (isotonic)
- Primary Uses:
- Hydration in fluid-depleted patients
- Energy supply in malnourished or fasting individuals
- Treatment of mild hypoglycemia
- Supportive therapy in ketoacidosis
- Diluent for compatible IV medications
- Clinical Setting: Commonly used in emergency care, ICUs, operating rooms, and general wards
How to use 5% w/v DEXTROSE INJECTION USP
5% Dextrose Injection USP 2000ml is administered intravenously and should only be used under the supervision of qualified healthcare personnel. It is essential to maintain sterile technique throughout its use to avoid contamination and associated complications.
- Route: Intravenous infusion (IV)
- Instructions for Use:
- Inspect the bag for clarity and check for any particles, discoloration, or leaks
- Remove the overwrap and connect the IV line using a sterile administration set
- Prime the IV tubing and connect to the patient's IV access
- Adjust the flow rate as prescribed by the healthcare provider
- Important Guidelines:
- Do not use if the solution is cloudy or the bag is damaged
- Do not administer with incompatible drugs
- Avoid using in series connections due to risk of air embolism
- Monitoring: Regularly check the patient’s hydration status, blood glucose, and electrolyte levels during infusion
Mode of Action 5% w/v DEXTROSE INJECTION USP
5% Dextrose Injection USP acts through two key mechanisms: fluid replenishment and metabolic energy supply. The glucose component serves as a readily available fuel source for the body, while the water content supports hydration.
- Metabolic Action:
- Dextrose is metabolized by cells into glucose
- Glucose enters cells via insulin-dependent and insulin-independent transporters
- Through glycolysis and the citric acid cycle, glucose is converted into ATP for energy
- Hydration Effect:
- Initially remains extracellular due to isotonicity
- As glucose is metabolized, free water redistributes across body compartments
- Helps correct mild dehydration and maintain fluid balance
- Anti-Ketotic Role:
- Prevents excessive fat breakdown in fasting states
- Reduces ketone body production by providing an alternate energy source
- Additional Benefits:
- Acts as a carrier for compatible IV medications
- Improves tolerance to parenteral nutrition in some patients
5% w/v DEXTROSE INJECTION USP Interactions 5% w/v DEXTROSE INJECTION USP
5% Dextrose Injection USP may interact with certain medications, electrolytes, and medical conditions. Awareness of these interactions helps avoid adverse outcomes and enhances treatment efficacy.
- Medication-Based Interactions:
- Insulin: Co-administration increases the risk of hypoglycemia
- Diuretics: Risk of electrolyte depletion, especially potassium and sodium
- Cardiac glycosides (e.g., digoxin): Hypokalemia may enhance toxicity
- Corticosteroids: May lead to fluid retention and hyperglycemia
- Incompatible Drugs: Avoid mixing with medications not confirmed to be stable in dextrose solutions (e.g., phenytoin, amphotericin B)
- Condition-Based Interactions:
- Patients with diabetes mellitus may experience hyperglycemia
- In renal or heart failure, excess fluid may lead to volume overload
- Lab Monitoring Recommendations:
- Monitor blood glucose frequently
- Assess serum electrolytes regularly
- Track daily fluid input and output
Dosage of 5% w/v DEXTROSE INJECTION USP
The dosage of 5% Dextrose Injection USP (2000ml) varies depending on the patient’s clinical needs, body weight, fluid balance, and metabolic demands. It should always be prescribed and monitored by a healthcare provider.
- Adults:
- Typically, 1000 to 3000 ml/day based on fluid and caloric requirements
- Infusion rate: 50 to 150 ml/hour
- Pediatrics:
- Dosage is weight-based: 100–150 ml/kg/day
- Carefully monitor glucose infusion rate (GIR)
- Neonates:
- Start with 60–100 ml/kg/day
- Strict monitoring to avoid fluid overload or hypo-/hyperglycemia
- Maximum Dosage:
- Depends on patient’s renal function and cardiovascular status
- Should not exceed recommended GIR: typically no more than 4–5 mg/kg/min in adults
- Adjustment Guidelines:
- Adjust dose in renal, hepatic, or cardiac impairment
- Consider electrolyte supplementation when needed
Possible side effects of 5% w/v DEXTROSE INJECTION USP
Although 5% Dextrose Injection USP is generally well-tolerated, side effects can occur, especially in vulnerable populations or with prolonged use. Regular clinical monitoring helps mitigate these risks.
- Common Side Effects:
- Redness or pain at the infusion site
- Mild hyperglycemia, particularly in diabetic patients
- Thirst or mild fluid retention
- Serious Side Effects:
- Fluid overload: Leading to pulmonary edema or hypertension
- Electrolyte disturbances: Especially hyponatremia or hypokalemia
- Phlebitis: Inflammation of the vein used for infusion
- Anaphylactic reactions: Rare but possible
- Preventive Measures:
- Use correct infusion rate
- Monitor blood glucose and serum electrolytes
- Rotate IV site and assess for signs of inflammation or infection
5% w/v DEXTROSE INJECTION USP Contraindications 5% w/v DEXTROSE INJECTION USP
5% Dextrose Injection USP should not be administered in certain medical conditions where glucose or free water may worsen the patient’s status. Identifying these contraindications is essential for safe clinical use.
- Absolute Contraindications:
- Known hypersensitivity to dextrose
- Severe hyperglycemia not managed by insulin
- Fluid overload states (e.g., pulmonary edema)
- Relative Contraindications:
- Uncontrolled diabetes mellitus
- Severe renal impairment with oliguria/anuria
- Congestive heart failure
- Intracranial pressure elevation or cerebral edema
- Special Considerations:
- Use with caution in neonates and the elderly
- Monitor glucose and fluid balance frequently in at-risk patients
Storage of 5% w/v DEXTROSE INJECTION USP
Proper storage of 5% Dextrose Injection USP (2000ml) ensures safety and efficacy. The product must be kept under specified conditions and inspected prior to use.
- Temperature: Store between 20°C to 25°C (68°F to 77°F)
- Allowable Excursions: Between 15°C to 30°C are acceptable temporarily
- Protection: Keep in protective overwrap until use to prevent exposure to light and moisture
- Do Not Freeze: Freezing may cause container leakage or solution degradation
- Visual Inspection: Check for clarity, absence of precipitates, and bag integrity before use
- Post-Opening Use: Use immediately after opening; do not reuse or store
5% w/v DEXTROSE INJECTION USP features an exceptional active ingredient renowned for its potent effects, comprising Dextrose. This powerful formulation provides a superior solution for addressing diverse health concerns. With 50mg/ml concentration and an easily manageable Infusion/Solution for, it remains a preferred option for countless individuals seeking effective treatment.
Introduction
All you need to know about 5% w/v DEXTROSE INJECTION USP .
Welcome to Dwaey, specifically on 5% w/v DEXTROSE INJECTION USP page.
This medicine contains an important and useful components, as it consists of Dextrose.
5% w/v DEXTROSE INJECTION USP is available in the market in concentration 50mg/ml and in the form of Infusion/Solution for.
QATAR PHARMA is the producer of 5% w/v DEXTROSE INJECTION USP and it is imported from QATAR,
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Frequently Asked Questions
5% w/v DEXTROSE INJECTION USP should be stored according to the instructions provided by QATAR PHARMA.
In general, it is recommended to store 5% w/v DEXTROSE INJECTION USP in a cool, dry place, away from direct sunlight
and out of the reach of children.
The duration of treatment with 5% w/v DEXTROSE INJECTION USP may vary depending on the condition being treated
and the guidance of your healthcare provider. It is important to follow the prescribed treatment
plan and continue taking 5% w/v DEXTROSE INJECTION USP for the recommended duration, even if your symptoms improve.
If you have any concerns or questions about the duration of treatment, consult your healthcare provider.
It is important to check with your healthcare provider or read the medication label for specific
instructions regarding alcohol consumption while taking 5% w/v DEXTROSE INJECTION USP. Some medications, including
5% w/v DEXTROSE INJECTION USP, may have interactions with alcohol that can reduce effectiveness, increase side
effects, or pose other risks to your health. It is best to follow the guidance provided by your
healthcare professional.
If you miss a dose of 5% w/v DEXTROSE INJECTION USP, take it as soon as you remember. However, if it is close
to the time for your next scheduled dose, skip the missed dose and continue with your regular dosing
schedule. Do not take a double dose to make up for a missed one unless advised by your healthcare provider.
No, do not stop taking 5% w/v DEXTROSE INJECTION USP without consulting your healthcare provider, even if your
symptoms improve. It is important to complete the full course of treatment as prescribed. Stopping
the medication prematurely may lead to a relapse or incomplete resolution of the condition. If you
have concerns about the duration of treatment, consult your healthcare provider for guidance.
It is important to consult your healthcare provider before taking 5% w/v DEXTROSE INJECTION USP if you are
pregnant or breastfeeding. They will be able to assess the potential risks and benefits based on your
specific situation. Please note that the safety and suitability of 5% w/v DEXTROSE INJECTION USP during pregnancy
or breastfeeding may depend on the active substance [Active Substance], concentration 50mg/ml,
and the specific recommendations of QATAR PHARMA.
The effects of 5% w/v DEXTROSE INJECTION USP on your ability to drive or operate machinery can vary depending on
the active substance [Active Substance], concentration 50mg/ml, and individual factors.
Some medications may cause drowsiness, dizziness, or other side effects that can impair your judgment
or coordination. It is important to read the medication label or consult your healthcare provider to
understand any potential effects on your ability to perform tasks that require alertness.
The instructions for taking 5% w/v DEXTROSE INJECTION USP with or without food may vary depending on the medication
and the recommendations of QATAR PHARMA. Some medications may be more effective when taken with
food to enhance absorption or reduce stomach irritation, while others may need to be taken on an empty
stomach for optimal absorption. Read the medication label or consult your healthcare provider for specific instructions.
The use of 5% w/v DEXTROSE INJECTION USP in children or elderly individuals may depend on various factors, including
the specific medication, type Infusion/Solution for, and the recommendations of QATAR PHARMA. Some
medications may have specific dosing instructions or precautions for these age groups. Consult your
healthcare provider or read the medication label for information regarding the safe and appropriate use
of 5% w/v DEXTROSE INJECTION USP in children or elderly individuals.
Dwaey
All medical information published on the Dwaey website aims to increase medical awareness and health education among users. However, it is not a substitute for professional medical advice. Always consult with a specialist doctor. We strongly advise against using any information or medicine found on the site without referring to your healthcare provider.
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