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Sodium Valproate 431 mg Oral Capsules

Sodium Valproate 431 mg Oral Capsules are a solid dosage form consisting of two halves of either gelatin or vegetarian-based shells that encapsulate the medication. This design ensures the capsules are easy to swallow and provide a precise dose of Sodium Valproate, which is essential for maintaining consistent therapeutic levels. Sodium Valproate is commonly used in the treatment of seizure disorders, including epilepsy, and is also indicated for the prevention of migraine headaches and the management of bipolar disorder. These capsules offer a convenient and effective way to administer the medication for these disease states.

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Formula Information

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Sodium Valproate 431 mg Oral Capsules are a solid dosage form consisting of two halves of either gelatin or vegetarian-based shells that encapsulate the medication. This form of medication is designed to be swallowed easily and to ensure that patients receive an exact dose of the active ingredient. Sodium Valproate is a well-established medication used primarily in the treatment of seizure disorders, including epilepsy. It works by increasing the levels of gamma-aminobutyric acid (GABA) in the brain, which helps to stabilize electrical activity and reduce the incidence of seizures.

In addition to its anticonvulsant properties, Sodium Valproate is also utilized in the management of bipolar disorder, where it can help to control episodes of mania or hypomania. It is sometimes used as a mood stabilizer in this context. Furthermore, Sodium Valproate may be prescribed for the prevention of migraine headaches, as it has been found to reduce the frequency of migraine attacks in some patients.

When considering Sodium Valproate therapy, it is important for both patients and prescribers to be aware of potential side effects, which can include gastrointestinal disturbances, weight gain, hair loss, and tremors. More serious but less common side effects may include liver toxicity and pancreatitis, which necessitate regular monitoring of liver function tests and patient symptoms. Due to the risk of birth defects, Sodium Valproate is not recommended for use during pregnancy unless clearly necessary and when the benefits outweigh the risks.

It is crucial for patients to adhere to the prescribed dosage and to not discontinue the medication abruptly, as this may lead to a worsening of their condition or precipitate withdrawal symptoms. Regular follow-up with the healthcare provider is essential to monitor the efficacy and safety of the treatment. Adjustments to the dosage may be required based on the patient's response and any side effects experienced.

At Bayview Pharmacy, we are committed to providing high-quality compounded medications tailored to the specific needs of our patients. Our team of knowledgeable compounding pharmacists is available to answer any questions and provide guidance on the use of Sodium Valproate 431 mg Oral Capsules. If you have any questions or require further information, please do not hesitate to reach out to us.

Drug Interactions

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Sodium valproate is an anticonvulsant and mood-stabilizing drug used to treat epilepsy and bipolar disorder, as well as to prevent migraine headaches. When considering the use of sodium valproate 431 mg oral capsules, it is important to be aware of potential drug interactions that may affect the efficacy of the medication or increase the risk of adverse effects.

One significant interaction is with other central nervous system (CNS) depressants, such as alcohol, benzodiazepines, and opioids. Concurrent use of these substances with sodium valproate can lead to increased sedation and an elevated risk of CNS depression. Patients should be advised to avoid or limit alcohol consumption and to use other CNS depressants with caution.

Enzyme-inducing antiepileptic drugs (AEDs) like phenytoin, carbamazepine, and phenobarbital can decrease the plasma concentration of valproate, potentially reducing its effectiveness. Conversely, valproate can increase the plasma concentration of other AEDs by inhibiting their metabolism, which may necessitate dosage adjustments of the concomitant AEDs to avoid toxicity.

Valproate is a known inhibitor of the liver enzyme UDP-glucuronosyltransferase (UGT), and therefore can interact with drugs that are substrates of this enzyme, such as lamotrigine. This interaction can lead to increased levels of lamotrigine in the blood, heightening the risk of serious skin rashes. Close monitoring and possible dose adjustments of lamotrigine may be required when used in combination with valproate.

Additionally, valproate can displace other highly protein-bound drugs from plasma proteins, such as warfarin, leading to an increased free fraction of these drugs and a potential increase in their effects. Patients taking warfarin or similar anticoagulants should be monitored for changes in coagulation parameters and may require dose adjustments.

Valproate may also affect the metabolism of drugs metabolized by the cytochrome P450 system, including certain antidepressants, antipsychotics, and hormonal contraceptives. This can result in altered plasma levels of these medications, which may necessitate monitoring and dosage adjustments.

It is also important to note that valproate can have a dose-dependent effect on the liver, and using it in combination with other hepatotoxic drugs can increase the risk of liver damage. Patients should be monitored for signs of hepatic dysfunction, especially in the first six months of treatment or when used in combination with other hepatotoxic medications.

Lastly, valproate's teratogenic potential must be considered in women of childbearing age. It can interact with folate metabolism, and its use during pregnancy is associated with an increased risk of birth defects. Effective contraception and preconception counseling are recommended for women of childbearing potential who are prescribed valproate.

Due to the complexity and potential severity of drug interactions with sodium valproate, it is crucial for prescribers to review a patient's complete medication profile before initiating treatment with valproate. Patients should be encouraged to report all medications they are taking, including over-the-counter drugs and herbal supplements. For any questions or concerns regarding drug interactions with sodium valproate 431 mg oral capsules, please reach out to us at Bayview Pharmacy for professional advice and guidance.

How Does it Work

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Sodium Valproate is an anticonvulsant medication that is used to treat various seizure disorders, including epilepsy, by stabilizing electrical activity in the brain. The mechanism by which Sodium Valproate exerts its therapeutic effects is multifaceted. Primarily, it is believed to increase the concentration of gamma-aminobutyric acid (GABA) in the brain. GABA is an inhibitory neurotransmitter that, when present in higher levels, can help to calm neuronal activity, thereby reducing the frequency and intensity of seizures.

In addition to its effects on GABA, Sodium Valproate also modulates the activity of the neurotransmitter glutamate, which is an excitatory neurotransmitter. By inhibiting the enzymes that break down GABA and blocking sodium channels, Sodium Valproate prevents excessive neuronal firing that can lead to seizures. Furthermore, it has been suggested that Sodium Valproate may also influence the function of calcium channels and have a direct effect on neuronal firing and signal transmission.

The 431 mg oral capsule formulation of Sodium Valproate provides a solid dosage form that is designed for ease of administration and consistent delivery of the active drug. The two-piece gelatin or vegetarian shells that make up the capsule are easily swallowed and dissolve in the digestive system to release the medication. This form of delivery ensures that the medication is absorbed into the bloodstream in a controlled manner, providing a precise dosage to the patient. The encapsulation also protects the active ingredient from degradation and ensures its stability until ingestion.

By using this formulation, patients with seizure disorders can manage their symptoms effectively. It is important for both patients and prescribers to understand that while Sodium Valproate can significantly reduce the occurrence of seizures, it is not a cure for epilepsy or other neurological conditions. Consistent use as directed by a healthcare professional is crucial for maintaining its therapeutic effects.

For those interested in using Sodium Valproate 431 mg Oral Capsules, it is essential to discuss with a healthcare provider to ensure it is the appropriate medication for your specific condition and to understand the potential side effects and monitoring requirements. If you have any questions or need further information about this formulation, please reach out to us at Bayview Pharmacy. Our team of compounding pharmacists is here to provide the support and guidance you need to manage your health effectively.

Other Uses

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In addition to being an established treatment for epilepsy and bipolar disorder, Sodium Valproate Oral Capsules may also be used off-label for other neurological and psychiatric conditions. The controlled release of active ingredients, provided by the solid dosage form, is beneficial in conditions where maintaining constant drug levels is necessary. One such use includes the prevention of migraine headaches. Some clinicians may prescribe Sodium Valproate as a prophylactic to reduce the frequency, severity, and duration of migraine episodes, although it is not FDA-approved for this indication.

Furthermore, there is some evidence suggesting that Sodium Valproate may have utility in treating various other conditions such as neuropathic pain, certain types of anxiety disorders, and as an adjunctive therapy in schizophrenia, particularly when there are symptoms of aggression or agitation. In these cases, Sodium Valproate acts on the central nervous system to stabilize mood and reduce hyperexcitability, which is thought to be beneficial. It should be noted, however, that the use of Sodium Valproate for these conditions should be considered with caution, taking into account the potential side effects and individual patient characteristics.

It is crucial for patients and prescribers to note that not all secondary uses of Sodium Valproate are supported by robust clinical evidence, and in many cases, further research is needed to firmly establish its efficacy and safety profile for these other uses. Prescribers must weigh the potential risks and benefits and consider individual patient responses when prescribing Sodium Valproate off-label. Additionally, due to known teratogenic effects, Sodium Valproate should not be used in pregnant women for any indication unless it is clearly necessary and there are no safer alternatives.

Quality compounding ensures that our Sodium Valproate 431 mg Oral Capsules meet the required standards for safety, efficacy, and patient adherence. As compounding pharmacists at Bayview Pharmacy, we are dedicated to providing personalized medications to suit the unique needs of each patient. Our expertise allows us to offer guidance on the appropriate use of our formulations. If you have any questions regarding the potential other uses of Sodium Valproate 431 mg Oral Capsules or its specific formulation, please do not hesitate to reach out to us.

Frequently Asked Questions

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What is Sodium Valproate 431 mg Oral Capsule?

Sodium Valproate 431 mg Oral Capsule is a medication used to treat seizure disorders, bipolar disorder, and prevent migraine headaches. It contains the precise dose of the active ingredient sodium valproate in a solid-form capsule.

How should I take Sodium Valproate 431 mg Oral Capsules?

Sodium Valproate 431 mg Oral Capsules should be taken orally with a glass of water. Swallow the capsule whole, without crushing or chewing. Always follow the dosing instructions provided by your healthcare provider.

Can I open the capsule if I have trouble swallowing it whole?

No, you should not open the capsule. The capsule is designed to release the medication in a controlled manner. If you have trouble swallowing it, contact your healthcare provider for alternatives.

Are these capsules available in a vegetarian option?

Yes, the oral capsules are available with both gelatin and vegetarian shells. Be sure to specify your preference when obtaining the prescription from the pharmacy.

What are the potential side effects of taking this medication?

Common side effects may include nausea, vomiting, dizziness, drowsiness, hair loss, and tremors. If you experience any severe side effects or signs of an allergic reaction, seek immediate medical attention.

Can I take Sodium Valproate 431 mg Oral Capsules with other medications?

Sodium Valproate may interact with other medications. It's important to discuss all current medications with your healthcare provider to prevent any adverse interactions.

How should I store the Sodium Valproate 431 mg Oral Capsules?

Keep the capsules in their original packaging, away from direct light and moisture, at room temperature. Make sure to keep them out of reach of children and pets.

What if I miss a dose?

If you miss a dose, take it as soon as you remember. However, if it is almost time for your next dose, skip the missed dose and continue with your regular dosing schedule. Do not take a double dose to catch up.

Is there any food or drink I should avoid while taking this medication?

You should avoid alcohol as it can increase the side effects of drowsiness and dizziness. Additionally, discuss any dietary restrictions with your healthcare provider.

How long will I need to take Sodium Valproate 431 mg Oral Capsules?

The duration of treatment with Sodium Valproate 431 mg Oral Capsules varies depending on the condition being treated and your individual response to the medication. It is important to continue taking it for as long as it is prescribed by your healthcare provider, even if you feel well.

Is it safe to use Sodium Valproate 431 mg Oral Capsules during pregnancy?

Sodium Valproate has been associated with significant risks during pregnancy. It is important to discuss the potential risks and benefits of this medication with your healthcare provider if you are pregnant, planning to become pregnant, or are breastfeeding.

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Formulas and/or material listed are not to be interpreted as a promise, guarantee or claim of therapeutic efficacy or safety. The information contained herein is not intended to replace or substitute for conventional medical care, or encourage its abandonment. Every patient is unique, and formulas should be adjusted to meet their individual needs.
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