Ursol Soft Capsules

Adult dose

Capsule: 1 capsule at a time, taken 3 times a day. Tablet: 1 tablet at a time, taken 3 times a day. Gel: 1 packet at a time, taken 3 times a day. Liquid: 1 bottle at a time, taken 3 times a day.

This medication should not be taken by patients with severe biliary obstruction or acute hepatitis. Persons allergic to this medication or its components, pregnant or lactating women, and children should not use it. Patients with Crohn's disease or colitis, radio-resistant calcified gallstones, non-functional gallbladder, and acute cholecystitis should not take this medication. Individuals with renal disease and patients with acute gastric or duodenal ulcers are advised not to take this medication as it may worsen symptoms. Persons allergic to soybean oil, beans, and peanuts should not take this medication. During the use of this medication, it should not be taken with oral diabetes medications, certain antacids, cholesterol-lowering medications, etc. It should also be avoided in conjunction with medications that can cause liver damage. People with severe pancreatic disease or gallstones, as well as patients with hyperlipidemia or lipid metabolism disorders, should consult a doctor or pharmacist before taking this medication. This medication contains Yellow No. 4 and Yellow No. 5 dyes; therefore, those allergic to these ingredients should use it with caution. If abnormal symptoms such as diarrhea, nausea, vomiting, abdominal pain, constipation, heartburn, dyspepsia, itching, rash, general malaise, dizziness, increased liver enzyme levels (ALT, ALP, AST, γ-GT), or decreased white blood cells occur during use, discontinue use immediately and consult a professional. Additionally, if symptoms like general malaise, dizziness, elevated liver enzyme levels, or decreased white blood counts appear, consult a professional immediately. Always adhere to the prescribed dosage and method of administration, and discontinue use promptly if any adverse reactions occur. Patients at risk of fatty overload should regularly monitor blood lipid levels and adjust the dosage as needed. This medication should be kept out of reach of children and stored in its original container to prevent misuse or deterioration in quality.

Serious side effects

• Interstitial pneumonia: fever
• cough
• difficulty breathing
• abnormal chest X-ray findings.

Mild side effects

Diarrhea, nausea, vomiting, abdominal pain, constipation, heartburn, discomfort in the stomach, itching, rash, general malaise, dizziness, increased liver enzyme levels (ALT, ALP, AST, γ-GT), decreased white blood cells.

Drug interactions

This medication may interact with oral diabetes agents (tolbutamide), cholestyramine, colestipol, activated charcoal, magnesium, and antacids containing aluminum hydroxide. Do not take with medications that reduce cholesterol in bile (e.g., estrogen-containing oral contraceptives) or those that lower blood cholesterol (e.g., clofibrate). Avoid concurrent use with medications that can cause liver damage.

This medication should be stored in a sealed container to prevent air and moisture from entering. Additionally, it must be stored in a cool, dry place below 15 degrees Celsius to maintain efficacy and prevent degradation.

Appearance

For domestic use: A soft capsule with a yellow viscous substance on one side that is yellow-green on one side and dark green on the other side. For export: A soft capsule with a yellow viscous substance on one side that is yellow on one side and brown on the other side.

Package unit

60 capsules/PTP (10 capsules/PTP x 6) - export type - 60 capsules/PTP [10 capsules/PTP x 6 - export type], 200 capsules/box (1 capsule/pack x 200) - 200 capsules/box [1 capsule/pack x 200], 30 capsules/PTP (10 capsules/PTP x 3) - 30 capsules/PTP [10 capsules/PTP x 3]