Leogink

      1. Drug name

    Leogink

    2. Drug formula ingredients

    Each bottle contains: Dried ginkgo leaf extract (Extractum folium Ginkgo biloba siccus , equivalent to 4.8 mg total Ginkgo flavone glycoside) 2 g

    Excipients: qs 50 ml .

    3. Dosage form

    Oral suspension.

    4. Route of administration

    Oral route.

    5. Indications

    • Cerebrovascular and peripheral vascular disorders.
    • Alzheimer's disease, dementia due to repeated infarction.
    • Tinnitus.

    6. Administration, dosage

    Dosage

    Adults and children over 12 years old: 1 ml x 3 times/day.

    Note: The above dosage is for reference only. Specific dosage depends on physical condition and disease progression. For the appropriate dosage, you need to consult your doctor or healthcare professional.

    Administration

    Medicines for oral use. Take medicine during meals . Note: Shake well before use.

    7. Contraindicated in the following cases:

    People who are sensitive to Ginkgo biloba extract should not use this medicine.

    Children under 12 years old.

    People with blood clotting disorders and bleeding.

    8. Warnings and precautions when using medicine

    Leogink is not an antihypertensive drug and cannot be used as a substitute for specific antihypertensive drugs.

    Do not use the medicine for children under 12 years old.

    9. Use medicine for pregnant and lactating women

    Pregnant

    The safety of using this drug in pregnant women has not been established, so the drug is not prescribed during pregnancy.

    Breastfeeding women

    Use of this medication by nursing mothers is not recommended, because it is unknown whether the drug passes into breast milk .

    10. Effects on ability to drive and use machines

    Caution should be exercised when using for those driving and operating machinery.

    11. Drug interactions and incompatibilities

    There is an interaction with anticoagulants or drugs that affect platelet aggregation.

    12. Undesirable effects

    Headache, dizziness, palpitations, digestive disorders, bleeding disorders and skin hypersensitivity reactions.

    Instructions on how to handle ADR

    When experiencing side effects of the drug, stop using it and notify your doctor or go to the nearest medical facility for timely treatment.

    13. Overdose and treatment

    There have been no reports of overdose.

    In case of emergency, immediately call the Emergency Center 115 or go to the nearest local medical station .

    14. Pharmacodynamic properties

    NA

    15. Pharmacokinetic properties

    NA

    16. Packaging specifications

    Box of 1 bottle x 50 ml with instructions for use.

    17. Storage conditions, expiration date, and quality standards of the drug

    Storage conditions: Cool and dry place, protected from light, temperature not exceeding 30 o C.

    Expiry date: 36 monthsfrom the date of manufacture.

    Quality standards of drugs: In House

    18. Name and address of the drug manufacturing facility

    Euro Santé Pharmaceutical Joint Stock Company

    Song Cung industrial site, Dong Thap commune, Dan Phuong district, Hanoi city, Vietnam.

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