Joinact 800 Tablets

Adult dose

Adults aged 19 years and older should take 1 tablet once a day.

This medication should not be taken by patients with high calcium levels in the blood (hypercalcemia), sarcoidosis (a systemic inflammatory disease of unknown origin), or people with kidney diseases. Additionally, individuals allergic to this medication or its components, infants under 12 months, patients with kidney stones, and those with severe renal failure should avoid taking this medication. People with allergies to soybean oil, soy, and peanuts should not take this medication, nor should it be administered to those with genetic disorders that prevent the breakdown of lactose. During the use of this medication, it is advisable to avoid taking it with phosphate, calcium salts, oral tetracycline formulations, antacids, and levodopa. Patients undergoing treatment, pregnant women or those who may become pregnant, nursing mothers, premature infants, and infants must consult with a physician or pharmacist before taking this medication. Patients with heart or circulatory issues, renal disorders, hypoproteinemia, or those taking cardiac glycosides should also consult professionals before taking this medication. If symptoms such as nausea, vomiting, diarrhea, skin rash, or irregular heartbeat occur while taking this medication, discontinue use immediately and consult healthcare professionals. Particularly, high doses of pyridoxine taken over a long period may lead to neurological disorders, so caution is required. This medication must be taken according to the prescribed dosage and regimen, and beverages containing tannins, such as green tea or black tea, should be avoided before and after taking it. Patients with lipid metabolism issues should regularly check their blood lipid levels while taking this medication, and dosage adjustments may be necessary if other lipid-lowering agents are concurrently administered. This medication should be stored out of the reach of children, away from direct sunlight, and in a cool, dry place. Additionally, for quality maintenance, do not transfer it to other containers, and misuse must be avoided.

Serious side effects

• Irregular heartbeat
• heart failure
• skin rash
• red spots
• edema
• fluid retention
• hypercalcemia
• stone disease

Mild side effects

Nausea, vomiting, diarrhea, loose stools, constipation, hypotension, facial flushing, irregular heartbeat, skin rash, red spots, heart failure, central nervous system depression, loss of appetite, erythema, eczema, rashes, papular rashes, itching, edema, fluid retention, sensory neuropathy or neurologic symptoms, hematologic adverse reactions, exacerbation of peptic ulcers, impaired glucose tolerance, hyperuricemia, liver damage, hypernatremia, congestive heart failure

Drug interactions

This medication should not be taken with phosphate, calcium salts, oral tetracycline formulations, antacids, or levodopa. Patients receiving cardiac glycosides should consult a physician or pharmacist before use. Consultation with a physician or pharmacist is also necessary when co-administering with aldosterone antagonists or triamterene.

Food interactions

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

This medication should be stored in a closed container to prevent air or moisture from entering, ideally at room temperature between 1°C and 30°C. This ensures the medication's effectiveness is safely maintained.

Appearance

Pale yellow oval film-coated tablet

Package unit

Bottle - 120 tablets/box [(60 tablets/bottle * 2)]