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Dproate ER 500 Tablet

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Prescription Required

Marketer

Celoris Pharmaceuticals Pvt Ltd

Salt Composition

Divalproex (500mg)

Overview Dproate ER 500 Tablet

Valproic acid extended-release 500mg tablets are prescribed for epilepsy management, effectively preventing and controlling seizures. This medication also finds application in migraine prophylaxis and, in some cases, bipolar disorder treatment. Dosage and frequency are determined individually by your physician to optimize symptom control, and may involve solo administration or combination therapy with other medications. While food intake doesn't affect absorption, consistent daily timing is crucial for efficacy. Therapeutic effects typically manifest within a couple of weeks. Consistent use, as directed, is vital; discontinuation or missed doses risk seizure recurrence and disease exacerbation; abrupt cessation is contraindicated. Common side effects, often mild, include headache, visual blurring, nausea, vomiting, dizziness, fatigue, instability, easy bruising, and hypothermia. Persistent or bothersome effects warrant medical consultation, while immediate medical attention is needed for skin rashes or redness. Prolonged use carries a risk of osteoporosis and increased fracture susceptibility. Rarely, suicidal ideation or behavior may occur; report any mood deterioration to your doctor promptly. Prior consultation is essential if you have a history of cardiac issues, renal or hepatic impairment, urinary difficulties, depression, or suicidal tendencies. Potential drug interactions necessitate informing your physician of all concurrent medications. Pregnant individuals should consult their doctor before initiating or discontinuing this medication. Alcohol consumption should be avoided due to its potential to worsen side effects and increase seizure risk. Regular blood tests, both pre- and post-treatment initiation, monitor therapeutic drug levels.

Uses of Dproate ER 500 Tablet

Managing epileptic seizures and bipolar disorder; migraine prevention.

Major Benefits of Dproate ER 500 Tablet:

Administer this medication precisely as prescribed by your physician, adhering to both the dosage and treatment duration. Ingest the tablet whole; avoid chewing, crushing, or fracturing it. Dproate ER 500 Tablets can be consumed with or without food, however, consistent daily timing is recommended.

Common Side effects of Dproate ER 500 Tablet:

  • Decreased body temperature
  • Dizziness
  • Sleepiness
  • Tremors
  • Paresthesia (tingling or pricking sensation)
  • Anemia (low number of red blood cells)
  • Decreased sodium level in blood
  • Liver injury
  • Gastrointestinal disturbance
  • Hypersensitivity
  • Deafness
  • Urinary incontinence
  • Increase in body weight
  • Pain during periods

How to use Dproate ER 500 Tablet:

Administer this medication precisely as your physician directs, adhering to the prescribed dosage and treatment schedule. Ingest the tablet whole; avoid chewing, crushing, or fracturing it. Dproate ER 500 Tablets can be consumed with or without food, although consistent timing is recommended.

How Dproate ER 500 Tablet works:

Deproate extended-release 500 mg tablets are used to manage epilepsy. This medication works by reducing overactive and irregular neuronal firing in the brain, thereby controlling seizures.

SAFETY ADVICE

AlcoholAlcoholUNSAFE

Concurrent use of Dproate ER 500 mg tablets and alcohol may lead to increased sleepiness.

PregnancyPregnancyCONSULT YOUR DOCTOR

Extended-release diproate 500 mg tablets pose a known risk to fetal development and should be avoided during pregnancy. In exceptional, life-threatening circumstances, a physician might prescribe it if the potential benefits outweigh the clear dangers to the unborn child. Physician consultation is essential.

Breast feedingBreast feedingSAFE IF PRESCRIBED

Extended-release divalproex sodium 500 mg tablets are considered safe for use while breastfeeding. Research in humans indicates minimal drug transfer to breast milk, posing no apparent risk to the infant.

DrivingDrivingUNSAFE

Driving ability may be impaired by side effects associated with Dproate ER 500 mg tablets.

KidneyKidneySAFE IF PRESCRIBED

Dproate ER 500 mg tablets are considered safe for use in individuals with impaired renal function. No alteration of the Dproate ER 500 mg tablet dosage is necessary.

LiverLiverUNSAFE

Extended-release divalproex sodium 500 mg tablets pose a likely risk for individuals with hepatic impairment and should be omitted. Physician consultation is advised.

What if you forget to take Dproate ER 500 Tablet :

Should you forget to take your Dproate ER 500 Tablet, administer it immediately. If, however, your next scheduled dose is imminent, omit the missed dose and resume your usual dosing regimen. Never take a double dose.

Facts to Know About Dproate ER 500 Tablet

LabelValue
Chemical Category Derivatives of Aliphatic Carboxylic Acids
Developing Habits No.
Treatment Category Neuroscience Central Nervous System
Action Class Antiepileptic drugs that modulate sodium channels

FAQs on Dproate ER 500 Tablet

Always consult your doctor before discontinuing Dproate ER 500 Tablet. Withdrawal should be gradual, under medical supervision, to avoid potential side effects such as symptom recurrence, irritability, anxiety, dizziness, and tremors.
Dproate ER 500 Tablets can act as a mood stabilizer in some cases, particularly for individuals experiencing rapid mood swings. The medication achieves this effect by reducing excessive brain activity associated with these mood changes.
Weight gain is a possible side effect of Dproate ER 500 Tablet, potentially stemming from increased appetite. Manage your diet and exercise to minimize this risk. Consult your doctor if weight gain is a concern.
Dproate ER 500 Tablets can cause drowsiness. Refrain from driving or activities requiring alertness until you understand their effect on you.
Hair loss is a possible side effect of Dproate ER 500 Tablets, typically temporary and related to dosage. Consult your doctor if this side effect concerns you or continues.
Liver damage is a potential side effect of Dproate ER 500 Tablet, particularly within the first six months of treatment. Symptoms such as nausea, vomiting, appetite loss, stomach pain, dark urine, facial swelling, and jaundice (yellowing of skin or eyes) may indicate liver problems. Baseline liver function tests are recommended before starting Dproate ER 500 Tablet, with regular testing during the initial six months, especially for at-risk individuals or those with pre-existing liver conditions.
Refrain from drinking alcohol during your Dproate ER 500 Tablet treatment. Combining alcohol with this medication may increase drowsiness, dizziness, or lightheadedness.
Before starting Dproate ER 500 Tablet treatment, your doctor may order blood tests. These may include a complete blood count (with platelets), bleeding time, and coagulation studies to minimize the risk of bleeding or bruising. Liver function tests are also recommended before and, for high-risk individuals or those with a history of liver disease, during the first six months of treatment.
Severe abdominal pain, nausea, and vomiting may indicate pancreatitis. Seek immediate medical attention if you experience these symptoms. Your doctor may order a serum amylase test; if positive for pancreatitis, medication should be stopped immediately.
Dproate ER 500 Tablet overdose can lead to headaches, blurred vision (from constricted pupils), reduced reflexes, confusion, and drowsiness. Muscle weakness, seizures, loss of consciousness, altered behavior, and respiratory problems like rapid breathing, shortness of breath, or chest pain may also occur. Seek immediate medical help if an overdose is suspected.
Dproate ER 500 Tablet
108
MRP 132
18% off