Valprol (40mg/ml) 200ml Syrup

Valprol (40mg/ml) 200ml Syrup

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  • Manufacturer Intas Pharmaceuticals Ltd.
  • Generic Name

    Divalproex Sodium 40mg

Healthwire Pharmacy Ratings & Reviews (1500+)

4.9/ 5
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Product Information

  • Description
  • Ingredients
  • Drug Class
  • Dosage Form
  • Uses
  • In case of Overdose
  • Missed Dose
  • How To Use
  • When Not to Use
  • Side Effects
  • Precautions & Warnings
  • Drug Interactions
  • Food Interactions
  • Storage/Disposal
  • Quick Tips, if any
  • Description

    Divalproex Sodium, the active ingredient in the 40mg syrup/suspension, exerts its therapeutic effects primarily through the enhancement of gamma-aminobutyric acid (GABA) activity in the brain. It inhibits the breakdown of GABA, a major inhibitory neurotransmitter, by blocking the enzyme GABA transaminase. This inhibition leads to increased GABA levels, which subsequently reduces neuronal excitability. Divalproex Sodium also interacts with sodium channels, decreasing their conductance and stabilizing neuronal membranes, thereby reducing the excessive firing of neurons. This mechanism is crucial in preventing and controlling seizures and managing certain mood disorders by restoring the balance between excitation and inhibition in the central nervous system.

  • Ingredients

    Divalproex Sodium 40mg

  • Drug Class

    Anticonvulsant / Antiepileptic

  • Dosage Form

    Suspension

  • Uses

    The following are the uses of Divalproex Sodium 40mg Syrup/Suspension:

    • Used for treating acute manic or mixed episodes associated with bipolar disorder.
    • Used to prevent migraine headaches and reduce their frequency.
    • Used as an anticonvulsant to control certain types of seizures.
    • Used for managing behavioral issues and stabilizing mood in certain mental health conditions.
    • Used for treating various types of epilepsy, including complex partial seizures and absence seizures.
    • Used to alleviate rapid cycling in bipolar disorder.
    • Used for managing manic episodes in combination with other medications.
  • In case of Overdose

    In the case of an overdose of Divalproex Sodium 40mg Syrup/Suspension, prompt medical attention is necessary. Symptoms may include extreme drowsiness, loss of coordination, blurred vision, and in severe cases, seizures or loss of consciousness. Immediate treatment should involve contacting a poison control center or seeking emergency medical help. It is important to provide healthcare professionals with details of the medication, the amount ingested, and the time of overdose to ensure appropriate medical intervention.

  • Missed Dose

    In the case of a missed dose of Divalproex Sodium 40mg Syrup/Suspension, it is recommended to take the missed dose as soon as you remember, but only if the next scheduled dose is not too close. If it's almost time for your next dose, skip the missed dose and continue with your regular dosing schedule. Do not double the dose to make up for a missed one, as this may increase the risk of side effects. It's important to maintain a consistent medication routine, but if you frequently miss doses, consult your healthcare provider for advice on how to improve adherence.

  • How To Use

    To administer Divalproex Sodium 40mg Syrup/Suspension, shake the bottle well, measure the prescribed dose using a measuring cup or oral syringe, and take it orally as directed by your healthcare provider, typically two to three times a day, with or without food, ensuring to follow the recommended dosage instructions.

  • When Not to Use

    Following are the conditions or situations when Divalproex Sodium 40mg Syrup/Suspension should not be used:

    • Should not be used in individuals with a known allergy to Divalproex Sodium or related substances.
    • Contraindicated in patients with a known history of liver disease or significant liver dysfunction.
    • Not recommended for individuals with urea cycle disorders or a family history of these disorders.
    • Should not be used in patients with known mitochondrial disorders, especially mitochondrial polymerase γ (POLG) mutations.
    • Contraindicated in patients with pancreatitis or a history of significant or recurrent pancreatitis.
    • Not suitable for individuals with a history of bone marrow suppression or significant blood disorders.
    • Should be avoided in patients with a history of suicidal thoughts or behaviors.
    • Not recommended for patients with a rare genetic problem of galactose intolerance, glucose-galactose malabsorption, or Lapp lactase deficiency.
  • Side Effects

    The side effects of Divalproex Sodium 40mg Syrup/Suspension may include:

    • Nausea and vomiting
    • Weight gain
    • Stomach pain or upset
    • Dizziness or drowsiness
    • Hair loss or thinning
    • Tremors or shaking
    • Vision changes
    • Weakness or fatigue
  • Precautions & Warnings

    Following are the precautions and warnings for Divalproex Sodium 40mg Syrup/Suspension:

    • Not recommended for individuals with known hypersensitivity or allergy to Divalproex Sodium or related compounds.
    • Patients with liver disease or liver function impairment should use with caution, as it may require dose adjustments.
    • Regular monitoring of liver function is essential during treatment, especially in pediatric patients.
    • May cause drowsiness or dizziness; patients should avoid driving or operating heavy machinery until they know how the medication affects them.
    • Should be used with caution in elderly patients, as they may be more susceptible to side effects.
    • Alcohol consumption should be avoided as it can increase the risk of adverse effects.
    • Patients with a history of urea cycle disorders or a family history of severe or fatal hepatotoxicity should not use Divalproex Sodium without consulting a healthcare professional.
  • Drug Interactions

    Following are the drug interactions for Divalproex Sodium 40mg Syrup/Suspension:

    • Divalproex Sodium can increase the plasma level of phenytoin, leading to potential toxicity.
    • It may reduce the effectiveness of carbamazepine, lamotrigine, and ethosuximide.
    • Combining with phenobarbital or primidone can result in decreased plasma levels of Divalproex.
    • It may enhance the effects of CNS depressants like benzodiazepines and barbiturates.
    • Aspirin and other salicylates may increase the binding of Divalproex to plasma proteins.
    • Divalproex can reduce the clearance of zolpidem, potentially leading to increased sedation.
    • Caution is advised when using with warfarin, as it may increase bleeding risk.
  • Food Interactions

    Following are the food interactions for Divalproex Sodium 40mg Syrup/Suspension:

    • Alcohol consumption should be avoided or limited while taking this medication, as it can increase the risk of liver damage and may intensify the sedative effects of Divalproex.
    • Grapefruit and grapefruit juice should be consumed with caution as they can interfere with the metabolism of Divalproex, potentially leading to increased blood levels of the drug and a higher risk of side effects.
    • Avoid high-fat meals as they may affect the absorption of Divalproex, possibly leading to fluctuations in blood levels and inconsistent therapeutic effects.
    • Some dairy products, particularly those high in calcium, may interact with Divalproex, as calcium can decrease the absorption of the medication. Consider separating calcium-rich foods from medication intake.
    • Be cautious with high-protein diets, as they can affect the metabolism of Divalproex and potentially alter its effectiveness.
    • Certain herbal supplements, such as valerian and St. John's Wort, may interact with Divalproex and increase the risk of side effects, particularly those related to the central nervous system.
    • Carbonated beverages and sugary drinks should be consumed in moderation, as they can potentially affect the absorption and metabolism of Divalproex, leading to inconsistent blood levels.
    • Always consult your healthcare provider for specific dietary recommendations and to discuss any potential food interactions that may be relevant to your individual health status.
  • Storage/Disposal

    Divalproex Sodium 40mg Syrup/Suspension should be stored with caution, ensuring a cool and dry environment, ideally at room temperature, shielded from direct sunlight and moisture. The medication's original container should be tightly sealed to maintain its integrity and prevent contamination. Avoid storage in bathrooms or near heat-emitting appliances, as temperature fluctuations can impact the medicine's effectiveness. Always verify the expiration date, and when disposing of unused or expired syrup, refrain from flushing or pouring it down the drain. Consult a pharmacist or healthcare professional for appropriate disposal methods, and keep the medication inaccessible to children to prevent accidental ingestion. Proper storage and disposal are crucial to maintain the integrity of the medication and ensure safety.

  • Quick Tips, if any

    Following are the quick tips for Divalproex Sodium 40mg Syrup/Suspension:

    • Consult a doctor for the right dosage and duration based on your medical condition.
    • Ensure you understand the prescribed dosage and clarify any doubts with your healthcare provider.
    • Administer the syrup with the provided measuring device for accurate dosing.
    • Store the syrup at room temperature, away from direct sunlight and moisture.
    • Do not freeze the medication and keep it in its original container.
    • Regularly monitor blood levels of Divalproex Sodium as directed by your doctor.
    • Inform your doctor about all medications you are taking to avoid potential interactions.
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