Prolamin S Tablet

Adult dose

Adults take 1 tablet once daily.

This medication should not be taken by patients with hypercalcemia (high calcium levels in blood) or sarcoidosis (a type of unexplained systemic inflammatory disease), and patients with renal disease should avoid its use. Individuals who are allergic to any of the components in this medication or show hypersensitivity reactions, infants younger than 12 months, patients with kidney stones, patients with severe renal failure, and those with allergies to soybean oil, beans, or peanuts should also avoid taking it. During the course of treatment with this medication, it is advisable not to take medications such as phosphates, calcium salts, oral tetracycline antibiotics, antacids, and levodopa simultaneously. Women who are under medical treatment, pregnant or potentially pregnant, breastfeeding mothers, premature infants, and infants should consult their doctor or pharmacist before taking this medication. Individuals with cardiac or circulatory function issues, renal impairment, hypoalbuminemia, or a history of kidney stones should also consult a specialist before taking this medication. Patients with lipid metabolism disorders such as hyperlipidemia, diabetic dyslipidemia, or pancreatitis, who need to take lipid emulsions also require caution. If symptoms such as nausea, vomiting, diarrhea, oral inflammation, red spots, arrhythmia, central nervous system dysfunction, gastrointestinal disturbances, hypotension, or pulmonary edema occur, immediately discontinue use and consult medical staff. Prolonged high doses of Vitamin B6 may cause peripheral nerve issues, and intake of more than a certain amount of Vitamin B12 can result in hematological abnormalities, necessitating caution. Furthermore, high doses may cause exacerbation of gastric ulcers, blood sugar control issues, hyperuricemia, liver damage, and other side effects. Overdosage can lead to symptoms such as nausea, vomiting, hypernatremia, heart failure, and edema, and caution is advised when taking with certain diuretics due to the risk of hyperkalemia. If overdosing or if symptoms do not improve after one month of use, consult healthcare professionals promptly. This medication must be taken strictly according to the prescribed dosage and method, as urine may turn yellow which can affect clinical test results. It is advisable to avoid consuming tannin-containing teas such as green tea or black tea before and after taking this medication. Patients at risk of lipid overload should check plasma lipid levels and adjust the dosage of this medication if necessary, especially when used in conjunction with other lipid injection preparations, lipid content must be taken into account for adjustment. Store this medication out of reach of children, in a tightly sealed container away from direct sunlight, in a cool and dry place. To prevent misuse and maintain quality, it is important not to transfer this medication to other containers.

Serious side effects

Cardiac arrhythmia (heart stop), pulmonary edema (swelling)

Mild side effects

Nausea, vomiting, diarrhea, loose stools, stomatitis (oral inflammation), red spots, cardiac arrhythmia (heart stop), central nervous system dysfunction, gastrointestinal disturbances, digestive disorders, upper abdominal pain, hypotension, pulmonary edema (swelling), sensory neuropathy or neurological symptoms, hematological adverse reactions, exacerbation of peptic ulcer, impaired glucose tolerance, hyperuricemia, liver damage, hypernatremia, congestive heart failure, edema, hyperkalemia

This medication must be stored in a tightly sealed container to prevent air and moisture from entering. It is important to maintain storage temperatures between 1 to 30 degrees Celsius. This way, the effectiveness of the medication can be retained for a longer time.

Appearance

Pale yellow oval film-coated tablet

Package unit

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