Valproic
Acid Clinical Drug Profile
🔹 Indications
🔹
Pharmacokinetics
🔹 Chemistry
🔹 MOA
🔹 Dosage
🔹 Side Effects
🔹 Drug
Interactions
🔹
Contraindications
🔹 Monitoring
🔹 Conclusion
Valproic acid is a medication that is commonly used to treat a range
of neurological and psychiatric conditions. Here is a clinical drug profile for
valproic acid:
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Indications:
Valproic acid is indicated for the treatment of epilepsy, bipolar
disorder, and migraine headaches.
- Treatment of epilepsy (partial seizures, generalized seizures)
- Treatment of bipolar disorder (manic or mixed episodes, maintenance therapy)
- Prophylaxis of migraine headaches (reducing frequency and severity of attacks)
- Off-label use in the treatment of schizophrenia, borderline personality disorder, and alcohol withdrawal.
Pharmacokinetics:
Valproic acid is well-absorbed after oral administration and is metabolized in the liver. It has a half-life of approximately 8-18 hours and is excreted in the urine.
Chemistry:
Valproic acid is a short-chain fatty acid with the chemical name 2-propylpentanoic acid. It is available as both an immediate-release tablet and a delayed-release capsule.
MOA:
The exact mechanism of action of valproic acid is not fully
understood, but it is thought to work by increasing the levels of
gamma-aminobutyric acid (GABA), an inhibitory neurotransmitter in the brain.
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Dosage:
The recommended dosage of valproic acid varies depending on the
indication and the patient's age and weight. The usual starting dose for
epilepsy is 10-15 mg/kg/day, while the starting dose for bipolar disorder is
750 mg/day.
Side
Effects:
The most common side effects of valproic acid include nausea,
vomiting, diarrhea, drowsiness, and tremors. It can also cause liver toxicity,
pancreatitis, and birth defects if used during pregnancy.
Here are the side effects of valproic acid in bullet points:
- Nausea, vomiting, stomach pain, indigestion
- Drowsiness, dizziness, tremors
- Hair loss or thinning
- Weight gain
- Changes in menstrual periods
- Blurred or double vision
- Liver damage or failure (rare but serious)
- Pancreatitis (inflammation of the pancreas)
- Increased risk of birth defects if used during pregnancy
- Increased risk of suicidal thoughts or behavior in patients with depression or bipolar disorder.
Drug
Interactions:
Valproic acid can interact with a number of other medications,
including carbamazepine, phenytoin, and warfarin. It can also increase the
levels of other medications metabolized by the liver, such as lamotrigine and
zidovudine.
Here are the drug interactions of valproic acid in bullet points:
- Carbamazepine, phenytoin, phenobarbital, and other antiepileptic drugs can increase the metabolism of valproic acid, reducing its effectiveness
- Aspirin and other nonsteroidal anti-inflammatory drugs (NSAIDs) can increase the risk of bleeding in patients taking valproic acid
- Warfarin and other blood thinners can increase the risk of bleeding in patients taking valproic acid
- Lamotrigine, zidovudine, and other medications metabolized by the liver can have increased levels when taken with valproic acid, increasing the risk of toxicity
- Alcohol and other CNS depressants can increase the sedative effects of valproic acid
- Erythromycin and other antibiotics can increase the levels of valproic acid in the blood, increasing the risk of toxicity.
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Contraindications:
Valproic acid is contraindicated in patients with liver disease or a history of pancreatitis. It should also be avoided during pregnancy and breastfeeding.
Monitoring:
Patients taking valproic acid should have regular monitoring of liver function tests, blood counts, and electrolyte levels. They should also be monitored for signs of pancreatitis, such as abdominal pain and nausea.
Conclusion:
Valproic acid is a useful medication for the treatment of epilepsy, bipolar disorder, and migraine headaches. However, it can cause significant side effects and interactions with other medications, so it should be used with caution and under the guidance of a healthcare provider.
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