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Depracort 750mg Tablet XR

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Prescription Required

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AGM Biotec

Salt Composition

Divalproex (750mg)

Overview Depracort 750mg Tablet XR

Epileptic seizures and migraine prophylaxis are key indications for the extended-release formulation of Cortidep 750mg tablets. This medication can also be employed, on occasion, as an adjunct in bipolar disorder management. Dosage and frequency are determined individually by your physician to optimize symptom control, potentially in conjunction with other therapies. Administer this medication at the same time daily, with or without food, for consistent efficacy; therapeutic effects typically manifest within a couple of weeks. Continuous use, as prescribed, is crucial to prevent seizure recurrence and condition exacerbation; abrupt cessation is strongly discouraged. Common, generally mild, adverse effects encompass headache, visual blurring, nausea, vomiting, vertigo, fatigue, instability, easy bruising, and hypothermia. While continued use is advised, report persistent or bothersome side effects to your doctor immediately; skin rashes necessitate prompt medical attention. Prolonged use may contribute to osteoporosis, increasing fracture risk, and, rarely, may induce suicidal ideation or behavior; report any depressive mood changes promptly. Prior to commencing treatment, disclose any history of cardiac, renal, or hepatic impairment, urinary difficulties, depression, or suicidal tendencies. Inform your doctor of all concomitant medications to avoid potential drug interactions. Consult your physician before altering medication usage during pregnancy. Alcohol consumption should be minimized to mitigate the risk of intensified side effects and increased seizure susceptibility. Regular blood monitoring is often necessary to optimize dosing, both pre- and post-treatment initiation.

Uses of Depracort 750mg Tablet XR

Managing epilepsy and seizures | Bipolar disorder therapy | Migraine prevention

Major Benefits of Depracort 750mg Tablet XR:

Follow your doctor's instructions precisely regarding dosage and treatment length for Depracort 750mg XR tablets. These tablets should be swallowed whole; avoid chewing, crushing, or breaking them. While Depracort 750mg XR tablets can be administered with or without food, consistency is key – take them at the same time each day.

Common Side effects of Depracort 750mg Tablet XR:

  • 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 Depracort 750mg Tablet XR:

Administer this medication precisely as directed by your physician, adhering to the prescribed dosage and timeframe. Ingest the tablet whole; avoid chewing, crushing, or fracturing it. Depracort 750mg Extended-Release Tablets can be consumed with or without food; however, consistent daily timing is recommended.

How Depracort 750mg Tablet XR works:

Extended-release Depracort 750mg tablets are used to treat epilepsy. They work by reducing hyperactivity within the brain's neuronal network, thus controlling seizures.

SAFETY ADVICE

AlcoholAlcoholUNSAFE

Concomitant use of Depracort 750mg extended-release tablets and alcohol may induce significant somnolence.

PregnancyPregnancyCONSULT YOUR DOCTOR

Extended-release Depracort 750mg tablets pose a confirmed risk to fetal development and should not be taken during pregnancy. In exceptional, life-threatening circumstances, a physician might prescribe it if the potential benefits outweigh the known hazards. Physician consultation is essential.

Breast feedingBreast feedingSAFE IF PRESCRIBED

Extended-release Depracort 750mg tablets are considered safe for use while breastfeeding. Research in humans indicates minimal drug transfer to breast milk, posing no known risk to the infant.

DrivingDrivingUNSAFE

Extended-release Depracort 750mg tablets can induce adverse reactions that might impair driving capabilities.

KidneyKidneySAFE IF PRESCRIBED

Extended-release Depracort 750mg tablets are considered safe for use in individuals with kidney impairment. No alteration in Depracort 750mg XR dosage is necessary.

LiverLiverUNSAFE

Extended-release Depracort 750mg tablets are contraindicated for individuals with hepatic impairment and should be omitted. Physician consultation is advised.

What if you forget to take Depracort 750mg Tablet XR :

Should you forget a Depracort 750mg XR Tablet dose, administer it promptly. Nevertheless, if your next scheduled dose is imminent, omit the missed dose and resume your usual dosing regimen. Avoid taking a double dose.

Facts to Know About Depracort 750mg Tablet XR

LabelValue
Chemical Type Derivatives of Aliphatic Carboxylic Acids
Developing Habits No.
Treatment Category Central Nervous System (CNS) Neurology
Actions Antiepileptic drugs that modulate sodium channels

FAQs on Depracort 750mg Tablet XR

Always consult your doctor before discontinuing Depracort 750mg Tablet XR. Withdrawal should be gradual, under medical supervision, to avoid potential symptoms like recurrence of original conditions, irritability, anxiety, dizziness, or tremors.
Depracort 750mg XR tablets can act as a mood stabilizer in some cases, particularly for individuals experiencing rapid mood swings. This effect is achieved by reducing excessive brain activity associated with these mood changes.
Yes, Depracort 750mg XR tablets can cause weight gain, possibly due to increased appetite. Maintain a healthy diet and exercise to minimize this risk. Consult your doctor if you have concerns about weight gain.
Depracort 750mg XR tablets can cause drowsiness. Refrain from driving or activities demanding concentration until you understand their effect on you.
Hair loss is a possible, though typically temporary and dose-dependent, side effect of Depracort 750mg Tablet XR. Consult your doctor if this side effect concerns you or continues.
Depracort 750mg Tablet XR can cause liver damage, particularly within the first six months of treatment. Symptoms may include nausea, vomiting, appetite loss, stomach pain, dark urine, facial swelling, and jaundice (yellowing of skin or eyes). Liver function tests are recommended before starting and regularly during the initial six months, especially for at-risk individuals and those with a history of liver disease.
Refrain from drinking alcohol during your Depracort 750mg Tablet XR treatment. Combining alcohol with this medication may increase drowsiness, dizziness, or lightheadedness.
Before starting Depracort 750mg Tablet XR treatment, your doctor may order blood tests. These may include a complete blood count (with platelet count), bleeding time, and coagulation tests to minimize the risk of bleeding or bruising. Liver function tests are also recommended before and periodically during the first six months of treatment, especially for high-risk individuals or those with a history of liver disease.
Severe abdominal pain, nausea, and vomiting could indicate pancreatitis. Seek immediate medical attention if you experience these symptoms. Your doctor may order a serum amylase test; a positive result necessitates immediate medication cessation.
Depracort 750mg XR tablet overdose can lead to headaches, blurred vision (from constricted pupils), reduced reflexes, confusion, and fatigue. Muscle weakness, seizures, loss of consciousness, altered behavior, and respiratory problems (rapid breathing, shortness of breath, chest pain) are also possible. Seek immediate medical help if an overdose occurs.
Depracort 750mg Tablet XR
84
MRP 97
13% off