TEVETEN 600MG TAB

TEVETEN 600MG TAB

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  • Manufacturer Abbott Laboratories
  • Generic Name

    Eprosartan 600MG

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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

    Eprosartan 600MG Tablet primarily works by blocking angiotensin II receptors, specifically the AT1 subtype. Angiotensin II is a potent vasoconstrictor hormone that plays a crucial role in regulating blood pressure. When Eprosartan binds to the AT1 receptors, it prevents angiotensin II from exerting its effects. This inhibition leads to vasodilation, which reduces peripheral resistance and lowers blood pressure. By blocking the actions of angiotensin II, Eprosartan helps to relax and widen blood vessels, improving blood flow and decreasing the workload on the heart. This mechanism of action contributes to the overall antihypertensive effect of Eprosartan, making it effective in the management of hypertension.

  • Ingredients

    Eprosartan 600MG

  • Drug Class

    Angiotensin II receptor antagonist.

  • Dosage Form

    Tablet

  • Uses

    The following are the uses of Eprosartan 600MG Tablet:

    • Used for treating high blood pressure (hypertension).
    • Used to lower blood pressure and reduce strain on the heart.
    • Used in cases where hypertension is not controlled by other medications.
    • Used to prevent and manage heart failure, improving heart function.
    • Used to reduce the risk of cardiovascular events like strokes.
    • Used to improve blood flow and relieve symptoms of hypertension.
    • Used as part of a comprehensive treatment plan for cardiovascular health.
  • In case of Overdose

    In the case of an overdose of Eprosartan 600MG Tablets, the patient may experience symptoms such as low blood pressure, dizziness, and increased potassium levels in the blood. The severity of the symptoms depends on the amount ingested. Prompt medical intervention is necessary, including monitoring vital signs, inducing vomiting or performing gastric lavage, and providing supportive care to manage symptoms and prevent further complications. It is crucial to seek medical help immediately if an overdose is suspected.

  • Missed Dose

    In the case of a missed dose of Eprosartan 600MG Tablet, it is important to take the medication 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 double the dose to make up for a missed one, as this may increase the risk of side effects. If you miss multiple doses, contact your healthcare provider for advice on how to get back on track with your medication regimen. It is generally recommended to take the missed dose as soon as possible to maintain the drug's effectiveness.

  • How To Use

    To take Eprosartan 600MG Tablet, swallow the tablet whole with a glass of water, preferably at the same time each day, following the dosage instructions provided by your healthcare professional, typically once daily.

  • When Not to Use

    Following are the conditions/situations when Eprosartan 600MG Tablet should not be taken:

    • Should not be used in patients with known allergy or hypersensitivity to Eprosartan or other angiotensin II receptor blockers.
    • Contraindicated in pregnant women, especially during the second and third trimesters, as it can cause fetal harm.
    • Not recommended for breastfeeding mothers, as it may pass into breast milk and harm the nursing infant.
    • Should be avoided in patients with severe renal impairment or patients with a history of liver disease or impaired liver function.
    • Not suitable for individuals with bilateral renal artery stenosis or unilateral renal artery stenosis in patients with a single functioning kidney.
    • Should not be used in patients with severe hyperkalemia (high potassium levels in the blood).
    • Contraindicated in individuals with a history of angioedema (swelling of the face, lips, tongue, or throat) related to previous treatment with angiotensin-converting enzyme (ACE) inhibitors or angiotensin II receptor blockers.
    • Not recommended for patients with a history of heart or blood vessel problems, such as severe aortic stenosis or renal artery stenosis.
    • Should be discontinued if significant hyperkalemia, jaundice, or a marked elevation of liver enzymes occurs during treatment.
  • Side Effects

    The side effects of Eprosartan 600MG Tablet may include:

    • Dizziness
    • Fatigue or weakness
    • Diarrhea
    • Nausea and vomiting
    • Dry cough
    • Headache
    • Increased sensitivity to sunlight
    • Skin rash
  • Precautions & Warnings

    Following are the precautions and warnings for Eprosartan 600MG Tablet:

    • Not recommended for individuals with known allergies to eprosartan or any other angiotensin II receptor blockers.
    • Patients with a history of liver or kidney disease should exercise caution, as dosage adjustments may be necessary.
    • Dehydrated patients should be adequately hydrated before starting this medication.
    • May cause dizziness or lightheadedness, so caution is advised when performing tasks requiring alertness.
    • Not recommended for use during pregnancy or breastfeeding without medical advice.
    • Elderly patients may be more susceptible to side effects, especially dizziness and changes in blood pressure.
    • Regular monitoring of kidney function and blood pressure is recommended while taking this medication.
  • Drug Interactions

    Following are the drug interactions for Eprosartan 600MG Tablet:

    • Eprosartan may increase lithium levels in the blood, potentially leading to lithium toxicity. Close monitoring of lithium levels is recommended.
    • Combining Eprosartan with diuretics may increase the risk of hypotension (low blood pressure). Blood pressure monitoring is necessary.
    • Concomitant use with potassium-sparing diuretics can lead to hyperkalemia (high potassium levels). Regular potassium level checks are advised.
    • NSAIDs may reduce the antihypertensive effect of Eprosartan. Blood pressure should be monitored closely.
    • Concurrent use with ACE inhibitors can potentially lead to renal impairment and hyperkalemia. Close monitoring of kidney function and potassium levels is essential.
    • This combination should be used with caution, especially in patients with impaired renal function.
    • Eprosartan may have additive effects with other antihypertensive medications, increasing the risk of hypotension.
    • Eprosartan may increase cyclosporine levels, requiring close monitoring to avoid cyclosporine toxicity.
  • Food Interactions

    Following are the food interactions to be aware of when taking Eprosartan 600MG Tablet:

    • Grapefruit and grapefruit juice consumption should be limited as they can elevate blood levels of Eprosartan, potentially leading to increased side effects, particularly affecting the kidneys.
    • Alcohol intake should be minimized as it may exacerbate the dizziness associated with Eprosartan, and could also negatively impact blood pressure regulation.
    • High-sodium foods should be consumed sparingly as they can counteract the blood pressure-lowering effects of Eprosartan, making the medication less effective.
    • Foods rich in potassium, such as bananas and oranges, should be eaten in moderation to prevent excessive potassium levels in the blood, a condition known as hyperkalemia.
    • Licorice, particularly in large amounts, may decrease the effectiveness of Eprosartan by reducing its absorption, leading to inadequate blood pressure control.
    • Avoid excessive caffeine intake, as it can interact with Eprosartan, causing increased heart rate and potential blood pressure fluctuations.
    • Inform your healthcare provider about any herbal supplements or vitamins you are taking, as some may interfere with Eprosartan's effectiveness, requiring dosage adjustments.
  • Storage/Disposal

    Eprosartan 600MG Tablets should be stored in a secure and dry location, preferably in a medicine cabinet or a designated storage area, away from direct sunlight, moisture, and heat sources like ovens or radiators. Keep the tablets in their original container, tightly sealed, to maintain their integrity and prevent exposure to environmental factors. Regularly check the expiration date on the packaging and do not use the medication if it is past its expiry. When disposing of unused or expired tablets, avoid flushing them down the toilet or sink. Instead, consult your pharmacist or local waste management guidelines for safe disposal practices to protect the environment. Ensure that the medication is kept out of children's reach to prevent accidental consumption.

  • Quick Tips, if any

    Following are the quick tips for Eprosartan 600MG Tablet:

    • Consult your doctor before starting this medication and provide your complete medical history.
    • Inform your doctor if you are pregnant, planning pregnancy, or breastfeeding.
    • Avoid alcohol consumption as it may increase side effects.
    • Do not operate heavy machinery or drive until you know how this medicine affects you.
    • Store the tablets in a cool, dry place, away from direct sunlight and moisture.
    • Do not share this medication with others, even if their symptoms are similar.
    • Regularly monitor your blood pressure and kidney function while on this medication.

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