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Product Information
Mycophenolate Mofetil, when administered, is rapidly metabolized in the liver and gut wall to mycophenolic acid (MPA), which is the active form of the drug. MPA acts as a non-competitive, selective, and reversible inhibitor of inosine-5'-monophosphate dehydrogenase (IMPDH). By blocking the activity of IMPDH, Mycophenolate Mofetil inhibits the de novo synthesis of guanosine nucleotides, which are essential for the proliferation of lymphocytes, especially T and B cells. This mechanism selectively suppresses the immune response by reducing the production of antibodies and inhibiting the activation and proliferation of T cells, thereby preventing the rejection of transplanted organs or tissues.
Immunosuppressant
Tablet
The following are the uses of Mycophenolate Mofetil 500mg Tablet:
Tailoring Treatment for Optimal Health, Prescribed Medication Dosage is:
In the case of an overdose of Mycophenolate Mofetil 500mg Tablets, individuals may experience severe gastrointestinal symptoms such as nausea, vomiting, and diarrhea. The severity of these symptoms can vary based on the amount ingested. Additionally, there is a risk of hematological complications, including leukopenia and thrombocytopenia. It is vital to seek medical assistance promptly, as doctors may employ specific treatments to manage the overdose, including gastric lavage and supportive care.
In the case of a missed dose of Mycophenolate Mofetil 500mg Tablet, it is generally recommended to take the missed dose as soon as you remember, provided it is not too close to the time of your next scheduled dose. If it is almost time for your next dose, skip the missed dose and continue with your regular dosing schedule. However, do not double the dose to make up for a missed one, as this may increase the risk of side effects. It is important to maintain a consistent medication routine, and if you frequently miss doses, consult your healthcare provider for advice on how to improve adherence to your treatment plan.
To take Mycophenolate Mofetil 500mg Tablets, swallow the tablet whole with a full glass of water, usually twice a day or as directed by your doctor, and ensure you take it consistently at evenly spaced intervals for optimal effectiveness.
Here are the situations when Mycophenolate Mofetil 500mg Tablet should not be used:
The side effects of Mycophenolate Mofetil 500mg Tablet may include:
Following are the precautions and warnings for Mycophenolate Mofetil 500mg Tablet:
Following are the drug interactions for Mycophenolate Mofetil 500mg Tablet:
Following are the food interactions for Mycophenolate Mofetil 500mg Tablet:
Mycophenolate Mofetil 500mg Tablets should be stored in a secure and dry location, away from direct sunlight and moisture. It is crucial to keep the medication in its original container, tightly sealed, to maintain its integrity and prevent contamination. Avoid storing the tablets in the bathroom or near heat-emitting appliances, as temperature fluctuations can impact their effectiveness. Pay attention to the expiration date on the packaging, and discard any unused or expired tablets appropriately. Do not dispose of them in sinks or toilets; instead, consult your pharmacist or healthcare professional for guidance on safe disposal practices. Always keep medications out of children's reach to prevent accidental consumption.
Following are the quick tips for Mycophenolate Mofetil 500mg Tablet:
Mycophenolate Mofetil is an immunosuppressant drug that is commonly used to prevent organ rejection in transplants. To ensure the safety and effectiveness of the drug, several essential laboratory tests are required. First, regular complete blood count (CBC) monitoring detects abnormalities in blood components, such as white blood cells, red blood cells, and platelets. Low white blood cell counts indicate immunosuppression, while low red blood cell counts may indicate anemia. Second, since Mycophenolate Mofetil can cause kidney damage, regular tests assess kidney function, including blood levels of creatinine and blood urea nitrogen (BUN) to determine creatinine clearance or estimated glomerular filtration rate (eGFR). Third, to ensure the drug does not cause undue stress to the liver, tests such as alanine aminotransferase (ALT), aspartate aminotransferase (AST), and bilirubin may be monitored. Additionally, specific levels of Mycophenolate Mofetil in the blood may be measured to ensure therapeutic concentration, particularly in the early stages of therapy or if there is a reason to suspect a compliance issue. Given the drug's potential to cause elevated potassium levels in the blood, periodic monitoring of potassium levels is recommended, especially in those with risk factors for hyperkalemia. Moreover, since concurrent use with certain immunosuppressants can lead to elevated calcium levels, occasional monitoring of calcium levels in the blood is recommended to rule out the risk of adverse events. Overall, these comprehensive tests help ensure the safe and effective use of Mycophenolate Mofetil in transplant patients.
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