Medication info
Jeniser Tablet 30 mg (Nisegoline)

Jeniser Tablet 30 mg (Nisegoline)

Prescription medicationTabletOral
Ingredient · strength
Nicergoline›30mg / 1 tablet
Manufacturer / importer
Albozen Korea Co., Ltd.
Appearance
Yellow round film-coated tablet
Packaging
30 tablets/bottle, 100 tablets/bottle
Approval status
Active

MFDS item code 202303432 · Approved 2023.12.22 · Insurance code 652607250

Summary

Main use
Treatment of dementia syndrome (including memory impairment and difficulty concentrating)
Who takes it
Adults
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 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.

Ingredients

Manufacturer
Albozen Korea Co., Ltd.

Efficacy & effects

Treatment of dementia syndrome (including memory impairment and difficulty concentrating)

  • Lack of motivation
  • atherosclerotic headaches in the elderly
  • memory impairment
  • concentration difficulties
  • judgment impairments
  • lack of initiative
View approved original text

This medication helps to improve motivation issues caused by chronic cerebrovascular disorders following cerebral infarction. It is also effective in alleviating atherosclerotic headaches in the elderly and is used as an adjunct treatment for hypertension. The 30 mg dosage is very useful in treating dementia symptoms such as memory impairment, concentration difficulties, judgment impairments, and lack of initiative in cases of primary degenerative vascular dementia and mixed dementia. By improving various brain function disorders and vascular-related symptoms, it contributes to the enhancement of the overall quality of life of patients.

How to take

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 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.

Precautions

This medication should not be used in certain patients. For example, individuals allergic to this medication or to ergot alkaloids, those with acute heart issues, those experiencing acute bleeding, individuals taking drugs that act on the sympathetic nervous system, people with very slow heartbeats, those who have not yet achieved hemostasis following a cerebral hemorrhage, and individuals with orthostatic hypotension should not take this medication. Additionally, caution is needed when using this drug in people with slightly slow heart rates or those with impaired kidney function. Gastrointestinal symptoms such as indigestion, diarrhea, and vomiting or hepatic dysfunction may rarely occur while taking this medication. Dizziness, blood pressure changes, drowsiness, headaches, rashes, and other side effects may also occur, so care should be taken. This medication can lower blood pressure too much when used with other antihypertensive agents, so it is important to frequently monitor blood pressure. It may also affect uric acid levels, so those with a history of gout should use it cautiously. Care should be taken when driving or operating machinery after taking this medication. This medication is metabolized in the liver and may interact with other drugs. In particular, it could enhance the effects of antihypertensive agents, so consulting a physician is advisable. Women who are pregnant or breastfeeding should consult a doctor before taking this medication. High doses may be harmful to the fetus, and it may pass into breast milk, requiring caution. Elderly individuals may have weakened bodily functions, so care should be taken regarding dosage when taking this medication. Its safety has not been sufficiently verified in children, so use is best avoided. In case of overdose, blood pressure may temporarily drop; in such cases, blood pressure should be monitored, and necessary actions should be taken. Finally, this medication should be kept out of reach of children, and it must be stored in its original container with the cap tightly closed to maintain its quality.

Side effects

Loss of appetite, diarrhea, constipation, nausea, vomiting, regional upper abdominal pain or cramping, thirst, elevated ALT, elevated AST, dizziness, orthostatic hypotension, hypertension, increased blood uric acid levels, hypotension, drowsiness, fatigue, headache, tinnitus, fatigue, insomnia, rash, urticaria, itching, flushing, warmth, nightmares, mood changes, indigestion

Not everyone experiences these, and they can vary from person to person.

Storage

This medication may be sensitive to air or moisture, so it should be stored in a tightly sealed container. It is also important to store it at room temperature, between 1 to 30 degrees Celsius, avoiding extreme heat or cold.

Appearance and packaging

Appearance

Yellow round film-coated tablet

Package unit

30 tablets/bottle, 100 tablets/bottle

Same-ingredient medicines

Even with the same ingredient, strength, dosage form and how it is taken can differ.

Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.

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This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.