Ralitonic Soft Capsule

Adult dose

Ages 8 and older and adults: take 1 capsule once a day.

Child dose

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

This medication should not be taken by women in the first three months of pregnancy or who may become pregnant, as vitamin A may pose a risk of congenital malformations if taken in doses exceeding 5,000 IU. Children, especially those under the age of 6, may suffer lethal poisoning from an overdose of iron-containing products, so keep this product out of reach of children. Patients with hypercalcemia, sarcoidosis, kidney diseases, known allergies to any components of this medication, infants under 12 months, patients with Wilson's disease or iron metabolism disorders, patients with kidney stones, severe renal failure, and those with allergies to soybean oil, soy, or peanuts should not take this medication. Do not take this medication with phosphates, calcium salts, oral tetracyclines, antacids, or levodopa while using this medication. Infants under 1 year, patients under medical treatment, children exposed to excessive sunlight, patients with hyperoxaluria, pregnant or nursing women, patients with gastrointestinal disorders, heart and circulatory system disorders, kidney impairment, hypoproteinemia, patients using cardiac glycosides, liver and gallbladder disease patients, gout, and patients with hyperlipoproteinemia or diabetic dyslipidemia should consult a professional before taking this medication. If symptoms such as nausea, vomiting, itching, skin rash, irregular heartbeat, convulsions, or coma occur during taking this medication, discontinue use immediately and consult a doctor. Additionally, if bleeding persists for a long time or menstrual changes occur, caution is needed as neuropathy or hematological abnormalities can occur with high doses of pyridoxine or vitamin B12 during long-term use. Always follow the prescribed dosage and administration, and parental supervision is required when administering to children. Since vitamin A provided in this medication is sufficient from dietary sources, caution should be exercised not to exceed 5,000 IU daily when used as adjuvant therapy. During use, avoid beverages containing tannins, such as green tea or black tea, and patients at risk of fatty overload should check plasma lipid levels and adjust dosages accordingly. Finally, this medication should be stored in a cool and dry place out of reach of children, avoiding direct sunlight and should not be transferred to other containers.

Serious side effects

Hives, severe swelling (edema), central nervous system dysfunction, convulsions, coma, heart contraction failure (cardiac arrest), pulmonary edema, edema with elevated blood pressure, hemolysis, kidney failure, jaundice, liver disease, cardiac and circulatory dysfunction, severe allergic reactions, severe skin adverse reactions, respiratory issues, serious neurological symptoms, and severe edema or urination abnormalities.

Mild side effects

Nausea, vomiting, itching, dry and rough skin, painful joint swelling (edema), diarrhea, abdominal discomfort, constipation, rash, redness, loose stools, hypotension, facial flushing, irregular heartbeat, skin rash, photosensitivity reactions, abdominal colicky pain, spasms, fever, coma, upper abdominal pain, red spots, central nervous system dysfunction, gastrointestinal disturbances, digestive disorders, skin rashes, swelling, changes in menstrual cycle with heavier flow or earlier onset, bleeding.

This medication can be sensitive to air and moisture, so it should be stored in a tightly sealed container. It is advisable to maintain a storage temperature between 1 and 30 degrees Celsius.

Appearance

Brownish-black oblong soft capsules containing yellowish-green contents

Package unit

90 capsules (10 capsules/PTP*9), 180 capsules (10 capsules/PTP*18)