Let It Be Proone Tablet

Adult dose

Ages 8 and older: take 1 tablet once a day.

This medication should not be taken by individuals with high blood calcium levels or kidney disease. Individuals who are allergic to any of the ingredients in this medication, children under 12 months old, patients with kidney stones, and those with severe renal failure should avoid it. People with lactose intolerance or specific genetic metabolic disorders should not take this medication. Those allergic to soybean oil, soy, or peanuts should also refrain from using this medication. Phosphates, calcium salts, certain antibiotics or antacids, and levodopa should not be taken concurrently with this medication. Infants under 1 year old, patients currently undergoing treatment, children exposed to a lot of sunlight, and pregnant or nursing women should consult a healthcare professional before taking this medication. Individuals with heart or kidney function issues, or a history of hypoproteinemia or kidney stones should exercise caution. If symptoms such as nausea, vomiting, diarrhea, skin rash, irregular heartbeat, or central nervous system dysfunction occur while taking this medication, it should be discontinued immediately and a healthcare professional consulted. Changes in menstruation or increased thromboembolism risk when taken with certain contraceptives should be approached with caution. High doses may lead to nerve damage, gastrointestinal disorders, liver damage, therefore the prescribed dosage must be strictly followed. This medication should be administered to children under the supervision of a guardian, and urine color may change, so this should be noted during clinical tests. It is advisable to avoid tannin-containing drinks like green tea or black tea before and after taking this medication. Patients with lipid metabolism issues should monitor their plasma lipid levels regularly and adjust their dosage accordingly. This medication should be stored in a cool, dry place away from children's reach, and direct sunlight should be avoided. To maintain quality, do not transfer to another container.

Serious side effects

• Dysrhythmia (cardiac arrest)
• central nervous system dysfunction
• pulmonary edema
• edema
• increased thromboembolism risk.

Mild side effects

Nausea, vomiting, diarrhea, loose stools, loss of appetite, abdominal distension, red spots, dysmenorrhea, central nervous system dysfunction, dermatitis, odor in sweat or breath, hair loss, restlessness, gastrointestinal disorders, digestive issues, upper abdominal pain, hypotension, pulmonary edema, menstrual changes, hematological adverse reactions, sensory neuropathy or neurological symptoms, peptic ulcer promotion, impaired glucose tolerance, hyperuricemia, liver damage, hypernatremia, congestive heart failure, edema, hypercalcemia.

Drug interactions

This medication should not be taken with phosphates, calcium salts, oral tetracyclines, antacids, or levodopa. Consult a doctor or pharmacist if taking oral contraceptives containing estrogen, anti-aldosterone agents, or triamterene.

Food interactions

Avoid consuming tannin-containing teas such as green tea and black tea during and before/after taking this medication.

This medication should be stored in a tightly sealed container to prevent exposure to air or moisture. It is recommended to maintain a storage temperature between 1 and 30 degrees Celsius.

Appearance

Dark yellow rectangular film-coated tablets

Package unit

60 tablets/bottle, 120 tablets/box [(60 tablets/bottle x 2)], 180 tablets/bottle