Jeniser Tablet 10 mg (Nisergoline)

Adult dose

* 5 mg, 10 mg Adults: Administer 5 ∼ 10 mg of nicergoline orally per dose, 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 example, it should not be administered to patients allergic to this medication or ergot alkaloids, those with acute myocardial infarction or acute bleeding, patients taking sympathomimetics, patients with significantly low heart rates, patients who have not achieved hemostasis after intracranial hemorrhage, and those with orthostatic dysregulation. Caution should be exercised when using this medication in patients with mild bradycardia or impaired renal function. During treatment, rare gastrointestinal symptoms such as anorexia, diarrhea, constipation, nausea, and vomiting may occur, and liver function test values may rise. Moreover, neurological symptoms such as dizziness, blood pressure changes, drowsiness, headaches, and insomnia may occur rarely. Allergic reactions such as rash, hives, itching, and flushing may occur, and if any abnormal symptoms arise, immediate consultation with a physician is necessary. Blood pressure may lower excessively if this medication is used with other antihypertensive agents, so frequent blood pressure monitoring is recommended. It may also affect uric acid metabolism, requiring caution in patients with a history of gout. Drowsiness may occur when driving or operating machinery, so caution is needed. This medication is metabolized in the liver by specific enzymes, thus potential interactions with other medications may occur, and you should inform your healthcare provider about any medications you are taking. Women who are pregnant or may become pregnant should carefully weigh the benefits and risks before taking this medication, and it is recommended to avoid use while breastfeeding or to stop breastfeeding if it must be used. Elderly patients may require dose adjustment due to potential declines in bodily functions. The safety of use in children has not been sufficiently confirmed, so caution is necessary in pediatric use. In cases of overdose, blood pressure may temporarily drop, thus blood pressure should be monitored, and appropriate actions should be taken. Finally, this medication should be stored out of reach of children, and stored in its original container to prevent misuse or degradation of quality.

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

This medication should be stored in a sealed container to protect it from air and moisture. It is recommended to maintain a storage temperature between 1 degree and 30 degrees Celsius at room temperature. This helps to maintain the effectiveness and safety of the medication.

Appearance

White round film-coated tablet

Package unit

30 tablets/bottle, 100 tablets/bottle