Magforce Active Soft Capsules

Adult dose

For individuals aged 12 years and older: take 1 capsule twice a day.

This medication should not be taken by individuals who have allergic reactions to this medication or any of its ingredients. Infants under 12 months old and patients with severe renal failure should not use this medication. Those allergic to soybean oil, soybeans, and peanuts should also avoid this medication. Patients with issues related to fat metabolism such as hyperlipidemia, diabetic dyslipidemia, and pancreatitis should use this medication with caution. This medication contains a dye called Yellow No. 5, so individuals allergic to this ingredient should be careful. It should not be taken with phosphates, calcium salts, oral tetracycline formulations, antacids, or levodopa. Women undergoing treatment, those who are pregnant or breastfeeding, and individuals with heart or kidney issues must consult with a healthcare professional before taking this medication. If any unusual symptoms such as stomach discomfort, diarrhea, rash, nausea, or vomiting occur while taking this medication, it should be discontinued immediately and a professional consulted. If menstruation occurs sooner than usual or bleeding lasts for an extended period, it should also be stopped and assessed. Notably, women taking oral contraceptives or patients at risk of thrombosis should be cautious, as taking vitamin E may increase the risk of thrombosis. Long-term, high-dose use of pyridoxine can lead to neurological disorders, so precautions should be taken. Patients deficient in folate who take high doses of vitamin B12 may experience hematological adverse reactions. Overdose may result in symptoms such as nausea, vomiting, edema, and heart failure, so caution is advised. Co-administration with certain diuretics may pose a risk of hyperkalemia, so a healthcare professional should be consulted. If symptoms do not improve after one month of use, the medication should be discontinued and advice sought. While taking this medication, plasma lipid levels should be regularly checked to monitor for fat overload, and dosing may need to be adjusted if necessary. If receiving other lipid medications, adjustments should be made based on the lipid content in this medication. The prescribed dosage and administration guidelines must be strictly followed, and it is advisable to consult with a physician or pharmacist during treatment. The urine may turn yellow during consumption, which could affect clinical test results. It is recommended to avoid tea containing tannins, such as green tea or black tea, before and after taking this medication. This medication should be stored out of reach of children, away from direct sunlight, in a cool, dry place. For quality maintenance, do not transferred to other containers.

Serious side effects

Cardiac arrest (cardiac arrest), central nervous system depression.

Mild side effects

Stomach discomfort, diarrhea, constipation, rash, redness (hyperemia), nausea, vomiting, loose stools, red spots, menstruation may occur earlier than expected or increase in amount, prolonged bleeding, sensory neuropathy or neurological symptoms, hematological adverse reactions, gastrointestinal symptoms such as nausea and vomiting, hypernatremia, congestive heart failure, edema, hyperkalemia, urine may change to yellow, effects on clinical test results.

Drug interactions

This medication should not be taken with phosphates, calcium salts, oral tetracycline formulations, antacids, or levodopa. Additionally, it should be discussed with a healthcare professional when used with oral contraceptives containing estrogen, anti-aldosterone agents, triamterene, or injectable lipid medications.

Food interactions

This medication should be avoided when taking tea containing tannins, such as green tea or black tea, during or before and after administration.

This medication should be stored in a tightly sealed container to avoid exposure to air and light, preferably at room temperature between 1 and 30 degrees Celsius. Additionally, it is safe and effective to use within 24 months from the manufacturing date.

Appearance

A reddish-brown oblong soft capsule containing a whitish emulsified substance (oil-like material)

Package unit

60 capsules (10 capsules/PTP x 6), 120 capsules ((10 capsules/PTP x 6) x 2)