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Telmisartan is an angiotensin II receptor blocker (ARB) that selectively blocks the activation of angiotensin II receptors, specifically the AT1 receptors. Its primary mechanism of action is to prevent the binding of angiotensin II, a potent vasoconstrictor hormone, to these receptors. Angiotensin II is involved in regulating blood pressure and fluid balance in the body. By blocking its effects, telmisartan promotes vasodilation, which leads to decreased peripheral resistance and reduced blood pressure. This mechanism helps to lower blood pressure by relaxing blood vessels, allowing for improved blood flow and reducing the workload on the heart.
Angiotensin II Receptor Blocker
Tablet
The following are the uses of Telmisartan 80mg Tablet:
Tailoring Treatment for Optimal Health, Prescribed Medication Dosage is:
In the case of an overdose of Telmisartan 80mg Tablets, it is important to seek medical advice promptly. Symptoms of an overdose may include low blood pressure, increased heart rate, and dizziness. The severity of the overdose effects can vary depending on the amount ingested and individual factors. Prompt medical intervention is necessary to manage the symptoms and ensure appropriate treatment, which may involve supportive care and monitoring of vital signs. It is crucial to act quickly to mitigate potential health risks.
In the case of a missed dose of Telmisartan 80mg Tablet, it is generally recommended to take the missed dose as soon as you remember. However, if it is almost time for your next scheduled dose, skip the missed dose and continue with your regular dosing schedule. It is important not to double the dose to make up for a missed one, as this may increase the risk of side effects. If you frequently miss doses, consider setting reminders or asking someone to remind you to take your medication to maintain the effectiveness of the treatment.
To take Telmisartan 80mg Tablet, swallow the tablet whole with a glass of water, preferably at the same time each day, as directed by your healthcare provider, without crushing or chewing the tablet.
Here is a list of situations or conditions when Telmisartan 80mg Tablet should not be taken:
The side effects of Telmisartan 80mg Tablet may include:
Following are the precautions and warnings:
Following are the drug interactions for Telmisartan 80mg Tablet:
Following are the food interactions to consider with Telmisartan 80mg Tablet:
Telmisartan 80mg Tablets should be stored in a cool and dry place, preferably at room temperature, ensuring protection from light and moisture. The original container should be tightly sealed to maintain its integrity and prevent contamination. It is crucial not to store the tablets in the bathroom or near heat-emitting appliances to preserve their effectiveness. Always adhere to the expiration date indicated on the packaging, and if the medication is no longer needed or has expired, proper disposal is essential. Avoid flushing the tablets down the toilet or sink; instead, consult a pharmacist or healthcare professional for guidance on safe disposal practices. Keep the medication securely stored away from children to prevent accidental consumption.
Following are the quick tips for Telmisartan 80mg Tablet:
Laboratory monitoring is an essential part of the management of patients taking Telmisartan 80mg. Specific tests and their frequency may vary depending on individual factors such as underlying medical conditions, other medications, and clinical circumstances. The six common lab tests detailed below are frequently required for comprehensive patient monitoring and to ensure patient safety. Firstly, Liver Function Tests (LFTs) are integral to monitoring liver health in patients taking Telmisartan. This is due to the drug's liver metabolism and potential to cause liver damage; ALT, AST, AKP, and bilirubin tests are all critical indicators of liver function and can highlight any signs of injury. Secondly, Kidney Function Tests (KFTs) are necessary to monitor kidney function in patients taking Telmisartan. This is particularly important because this drug can cause kidney impairment in cases of overdose or for patients with preexisting kidney problems. Blood urea nitrogen (BUN) and creatinine (Cr) levels provide crucial insight into overall kidney function. Thirdly, while not a laboratory test, it is vital to regularly monitor the patient's blood pressure, particularly for those with preexisting cardiovascular diseases or hypertension. As a blood pressure-lowering agent, Telmisartan may require dosage adjustments to maintain target blood pressure levels. Furthermore, a Complete Blood Count (CBC) is recommended to monitor any abnormalities in blood cell production, such as anemia. The prevalence of low red blood cell counts or anemia as a side effect of blood pressure medications including Telmisartan underscores the importance of this test. Potassium levels should also be monitored, especially if the patient is already taking potassium-sparing diuretics or other drugs that can affect potassium levels. Telmisartan can increase the risk of low potassium levels, known as hypokalemia. Finally, although less common, excessive sodium levels in the blood, known as hypernatremia, may affect some individuals taking Telmisartan.
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