Nicer Medications 10 mg (Nicergoline)

Adult dose

* 5 mg, 10 mg Adults: Administer 5 ∼ 10 mg of nicergoline orally 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, the dose 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 certain patients. For instance, individuals allergic to this medication or to ergot alkaloids should not be administered this drug. Additionally, patients with acute myocardial infarction, acute bleeding, and those taking sympathomimetic agents may be at risk when using this medication. Patients with very slow heart rates, those who have not stopped intracranial bleeding, and individuals with orthostatic control disorders should also avoid this drug. Patients with mild bradycardia or those with kidney function issues should be more cautious when using this medication. Occasionally, symptoms such as indigestion, diarrhea, constipation, nausea, vomiting, and dry mouth may occur after taking this medication. Liver function tests may show elevated levels, and dizziness, blood pressure changes, fatigue, headaches, and insomnia may rarely occur. Allergic reactions such as skin rashes or itching may also occur. This medication can lower blood pressure, so when taken with other antihypertensive medications, blood pressure should be monitored frequently. Additionally, it may affect uric acid levels, so individuals with a history of gout should exercise caution. After taking this medication, care should be taken when driving or operating machinery. Since this medication is metabolized in the liver, it may interact with other drugs, especially enhancing the effects of antihypertensive agents. Pregnant women or those who may become pregnant should carefully consider the risks and benefits before using this medication, and nursing mothers should ideally avoid administration or stop breastfeeding. Elderly patients may have decreased bodily functions, so dosage adjustments and vigilance are necessary. Its safety has not been established for children, and it is advisable not to use it in this population. In the case of overdose, blood pressure may temporarily drop, requiring monitoring and appropriate action. This medication must be kept out of the reach of children and stored in its original packaging sealed to avoid misuse or degradation in quality by transferring to another container.

• Loss of appetite
• diarrhea
• constipation
• nausea
• vomiting
• localized upper abdominal pain or cramps
• dry mouth
• ALT elevation
• AST elevation
• dizziness

This medication should be stored in a closed container to protect it from air and moisture. Additionally, the medication should be stored at room temperature between 1 and 30 degrees Celsius. It is advisable to avoid extremely warm or cold places.

Appearance

White round film-coated tablets

Package unit

30 tablets/bottle, 100 tablets/bottle