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B Braun Ecoflac Plus Ns 0.9% 500ml Injection
B Braun Ecoflac Plus Ns 0.9% 500ml Injection: Image 1
B Braun Ecoflac Plus Ns 0.9% 500ml Injection: Image 2
B Braun Ecoflac Plus Ns 0.9% 500ml Injection: Image 3

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Brand B.Braun

B Braun Ecoflac Plus Ns 0.9% 500ml Injection contains Sodium Chloride 0.9%, used for short-term fluid replacement and to restore salt and electrolyte levels in the body.

 

Benefits

Ecoflac Plus Ns 0.9% Infusion helps restore fluid balance and aids in improving the patient's overall health. It protects against dehydration and electrolyte imbalance following trauma or injury.

 

Uses and Indications

  • Short-term fluid replacement after trauma or injury.
  • Treatment of hypovolemia resulting from dehydration or injury.
  • Restoring salt and electrolyte levels in the body.
  • Extracellular fluid replacement.
  • Management of metabolic alkalosis in the presence of fluid loss and mild sodium depletion.
  • Priming solution in hemodialysis procedures.
  • Source of water and electrolytes for hydration.
  • Initiating and terminating blood transfusions without hemolyzing red blood cells.
  • Pharmaceutic aid and diluent for compatible drug additives.

The B Braun Ecoflac Plus Ns 0.9% 500ml Injection contains:

  • Sodium Chloride USP 0.9 g per 100 mL (equivalent to 4.5 g per 500 mL) (active ingredient).
  • Water for Injection USP qs.
  • pH adjusted with Hydrochloric Acid NF.
  • Electrolytes (per liter): Sodium 154 mEq, Chloride 154 mEq.
  • Calculated Osmolarity: 308 mOsmol/liter.
  • Sterile, nonpyrogenic, and isotonic.
Active Ingredient(s)Sodium Chloride 0.9%
Therapeutic ClassFluid Replacement, Electrolyte Replenisher
Route of AdministrationIntravenous
Storage ConditionsStore at room temperature (25°C), avoid excessive heat
Regulatory ApprovalU.S. Food and Drug Administration (FDA) approved for 0.9% Sodium Chloride Injection, USP in Ecoflac™ Plus 500 mL container
Diluent CompatibilityCompatible with various drug additives (consult pharmacist)
Licensed IndicationsExtracellular fluid replacement, treatment of metabolic alkalosis in presence of fluid loss and mild sodium depletion, source of water and electrolytes for hydration, priming solution in hemodialysis procedures, diluent for compatible drug additives

Dosage and Administration

  1. This solution is for intravenous use only and must be administered under the supervision of a healthcare professional.
  2. Dosage is determined by a physician, based on the patient's age, weight, clinical condition, and laboratory results.
  3. Visually inspect the solution for particulate matter or discoloration before use. Do not administer if the solution is not clear or if the container and seals are damaged.
  4. Use aseptic technique during administration.
  5. Do not connect flexible plastic containers in series to avoid the risk of air embolism.
  6. If adding other medications, consult a pharmacist for compatibility. Mix thoroughly and do not store solutions containing additives.

 

Storage and Disposal

  • Store at room temperature (25°C).
  • Avoid excessive heat and protect from freezing.
  • Keep all medications out of reach of children.
  • Discard any unused portion after use.
  • Dispose of waste and residues in accordance with local authority requirements.

Precautions and Safety

  • Do not use this injection if you have a known allergy to Sodium Chloride or any other ingredient in the formulation.
  • Administer with caution in patients with renal or cardiovascular insufficiency, congestive heart failure, hypervolemia, urinary tract obstruction, or those receiving corticosteroids.
  • Fluid balance, electrolyte concentrations, and acid-base balance should be monitored during prolonged parenteral therapy.
  • Excessive administration can lead to fluid and/or solute overload, hypernatremia, and electrolyte disturbances. Avoid in patients at risk for such conditions.
  • If you are pregnant or breastfeeding, inform your doctor before receiving this medicine, as dose adjustment may be required.

 

Side Effects and Risks

  • Common side effects may include injection site reactions such as redness, pain, swelling, irritation, or streaking. Other reported effects include hypotension, fever, tremor, chills, urticaria, rash, and pruritus.
  • Less common side effects can include nausea, vomiting, diarrhea, cramps, increased thirst, dry mouth or eyes, decreased urination, increased sweating, increased heart rate, difficulty breathing, swelling of hands, ankles, or feet, dizziness, lightheadedness, drowsiness, restlessness, irritability, headaches, confusion, muscle weakness, twitching, rigidity, or convulsions.
  • Serious allergic reactions are rare but can occur, presenting as rash, itching or swelling (especially of the face, tongue, or throat), severe dizziness, or trouble breathing. Seek immediate medical attention if these occur.
  • Report any bothersome or persistent side effects to your doctor or pharmacist.

 

Disclaimer

Use this medicine only under the prescription and guidance of a qualified doctor or pharmacist.

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