Sarlind Tablet 30 mg (Nisegoline)

Adult dose

* 5 mg, 10 mg Adults: Administer 5 ∼ 10 mg of nicergoline per dose orally 2 ∼ 3 times daily before meals. Adjust the dose as appropriate according to symptoms. * 30 mg Adults: Administer 30 mg of nicergoline orally once daily before meals. If the desired effect is not achieved at this dose, the dose may be increased to 60 mg. The dose may be reduced after symptoms improve. For patients with impaired renal function (serum creatinine >175 µmol/L) (2 mg/dL), administer a reduced dose.

This medication should not be used in certain patients. Patients with allergies to this drug or ergot alkaloids, those with acute myocardial infarction or acute hemorrhage, those taking sympathomimetic agents, patients with very low heart rates, patients who have not completed hemostasis after intracranial hemorrhage, and those with orthostatic dysregulation should not be administered this medication. Patients with mild bradycardia or impaired kidney function should use this medication with caution. Rarely, this medication can cause gastrointestinal symptoms such as dyspepsia or diarrhea, vomiting, increased liver function tests, dizziness, fluctuations in blood pressure, drowsiness, headaches, and skin rashes. When taken with other medications that lower blood pressure, blood pressure may become too low, so blood pressure should be checked frequently. Additionally, it may affect uric acid levels, so patients with a history of gout or hyperuricemia should use caution. After taking this medication, caution should be exercised when driving or operating machinery. This drug may interact with other medications during its metabolic process in the liver, so it is essential to consult with a professional about any concurrent medications. Women who are pregnant or could become pregnant should only use this drug when the therapeutic benefits outweigh the risks to the fetus. If breastfeeding, it is advisable to avoid taking this medication or to discontinue breastfeeding because this drug may be excreted in breast milk. Elderly patients, whose physical function may be reduced, require special attention, including dosage adjustments. The safety of this medication has not been sufficiently established in pediatric patients, so its use is not recommended. In cases of overdose, blood pressure may temporarily drop, and if symptoms appear, immediate consultation with healthcare professionals is necessary to obtain appropriate care. This medication should be stored in a safe place out of reach of children, in its original container, with the lid securely closed. Transferring it to another container may compromise the quality of the medication or pose a risk of misuse.

Loss of appetite, diarrhea, constipation, nausea, vomiting, generalized upper abdominal pain or cramps, dry mouth, ALT elevation, AST elevation, dizziness, orthostatic intolerance, hypertension, elevated blood uric acid, hypotension, drowsiness, malaise, headache, tinnitus, fatigue, insomnia, rash, urticaria, itching, flushing, heat sensation, nightmares, mood disturbances, dyspepsia

This medication may be sensitive to air or moisture, so it must be stored in a tightly sealed container. It's best to keep it at room temperature between 1 to 30 degrees Celsius. Storing it this way can maintain the medication's effectiveness safely.

Appearance

Yellow round film-coated tablet

Package unit

30 tablets/bottle, 100 tablets/bottle