Niseronide 30mg (Nisergoline)

Adult dose

* 5 mg, 10 mg Adults: Administer 5 ∼ 10 mg of nicergoline 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 a meal. If the desired effect is not achieved at this dose, it may be increased to 60 mg. The dose may be reduced after symptoms improve. Reduce the dose in patients with impaired renal function (serum creatinine >175 µmol/L) (2 mg/dL).

This medication should not be used in patients who are allergic to this drug or ergot alkaloids. It should also not be administered to patients with acute cardiac issues, acute hemorrhage, or those taking sympathomimetic drugs. It is advisable to avoid administering this drug to patients with very slow heart rates, uncorrected cerebral hemorrhage, and those with orthostatic hypotension. Caution should be exercised when using this drug in patients with slightly slow heart rates or reduced kidney function. This drug can rarely cause symptoms such as dyspepsia, diarrhea, constipation, vomiting, and dry mouth. Liver function test values may increase, so attention to liver health is required. Neurogenic symptoms such as dizziness, blood pressure changes, fatigue, drowsiness, headaches, and insomnia may also occur infrequently. Allergic reactions such as skin rashes, itching, hives, and flushing may occur, and if abnormal symptoms arise, they should be reported immediately. Since this drug has a blood pressure-lowering effect, blood pressure should be checked frequently when taken with other antihypertensive medications. It may affect uric acid levels, so patients with a history of gout should be cautious. After taking this medication, caution is needed while driving or operating machinery. This drug is metabolized by specific enzymes in the liver, potentially leading to interactions with other medications. Women who are pregnant or may become pregnant should consult a doctor before taking this medication, and those who are breastfeeding should avoid taking it or consider stopping breastfeeding while on it. Elderly individuals may have decreased physical function, thus careful dosing and monitoring is advised. The safety of this drug in children has not been established; therefore, its use is not recommended. In case of overdose, blood pressure may temporarily decrease, and immediate medical attention should be sought if symptoms occur. This drug should be kept out of the reach of children and stored tightly sealed in its original container.

• Loss of appetite
• diarrhea
• constipation
• nausea
• vomiting
• abdominal pain or cramps
• thirst
• elevated ALT
• elevated AST
• dizziness

This medication is sensitive to light and should be stored in a dark container that does not allow light in. Furthermore, it is important to keep it at room temperature between 1 to 30 degrees Celsius to maintain its efficacy.

Appearance

Yellow circular film-coated tablet

Package unit

100 tablets/bottle, 30 tablets/bottle