Instructions for use Trinefron-Health capsules blister No. 60
Composition
active ingredients: 1 capsule contains crushed medicinal plant raw materials:
Centaury (Centaurii herba) 18 mg;
rosemary leaves (Rosmarini folium) 18 mg;
lovage root (Levistici radix) 18 mg;
excipients: lactose monohydrate; povidone; corn starch; colloidal anhydrous silicon dioxide; magnesium stearate; capsule shell containing sunset yellow FCF (E 110), titanium dioxide (E 171), gelatin, black ink (in case of applying the company's trademark - ZT; contains shellac Glaze 45% solution in ethanol, black iron oxide (E 172), propylene glycol, concentrated ammonia solution).
Dosage form
Capsules.
Main physical and chemical properties: hard gelatin capsules of orange color. The contents of the capsules are a mixture containing granules and powder from light brown to brown. The presence of agglomerates of particles is allowed. The enterprise trademark - ZT - is allowed to be applied to the capsule.
Pharmacotherapeutic group
Drugs used in urology. ATX code G04B X50.
Pharmacological properties
Pharmacodynamics. The components that make up the herbal medicine exhibit complex activity, which is manifested in anti-inflammatory, antioxidant, antispasmodic and analgesic effects. The drug also has antibacterial and diuretic effects, which are due to the substances contained in the herbal components of the drug.
Indication
For the complex treatment of inflammatory diseases of the urinary tract.
Prevention of urinary stone formation, including after their removal.
Contraindication
Hypersensitivity to any component of the drug or to other plants of the Apiaceae family, such as anise, fennel, and to anethole (i.e. a component of essential oils containing, for example, anise and fennel).
Peptic ulcer in the acute stage.
Edema due to heart failure or kidney dysfunction and/or a doctor's recommendation to limit fluid intake.
Interaction with other medicinal products and other types of interactions
Unknown.
If it is necessary to use any other medicines at the same time, you should consult a doctor.
Application features
In case of prolonged fever, cramps, blood in the urine, urination disorders and acute urinary retention, you should immediately consult a doctor.
If the patient has been diagnosed with an intolerance to some sugars, contact your doctor before taking this medicinal product.
The drug contains the dye Sunset Yellow FCF (E110), which may cause allergic reactions.
Use during pregnancy or breastfeeding
Pregnancy. Experience in pregnant women indicates that there is no risk of fetal malformations or fetal/neonatal toxicity of the capsules. It is known that experimental studies have not shown any signs of reproductive toxicity. The use of the drug during pregnancy is possible after consultation with a doctor.
Breastfeeding. Due to the lack of data on the excretion of the drug or its metabolites into breast milk, a risk to the infant cannot be excluded. Therefore, the drug should not be used during breast-feeding.
The ability to influence the reaction speed when driving or working with other mechanisms
The drug does not affect the ability to drive or operate other mechanisms.
Method of administration and doses
Unless otherwise prescribed by a doctor, the drug should be taken by adults and children over 12 years of age - 2 capsules 3 times a day (total daily dose - 6 capsules). The capsules should be swallowed without chewing, with a sufficient amount of liquid (for example, a glass of water). It is necessary to ensure the consumption of sufficient liquid at the same time as taking the drug.
The duration of treatment is determined by the doctor individually. If the drug is well tolerated, it can be prescribed for a long period.
Children
The drug is not recommended for use in children under 12 years of age.
Overdose
Cases of drug poisoning due to overdose are unknown.
Therapy: symptomatic.
Side effects
Gastrointestinal disturbances (nausea, vomiting, diarrhea) are common. Allergic reactions may occur in case of hypersensitivity to the components of the drug, including urticaria, itching, and skin hyperemia.
If any adverse reactions occur, discontinue use of the drug and consult a doctor.
Expiration date
4 years.
Storage conditions
Store in the original packaging at a temperature not exceeding 25 °C.
Keep out of reach of children.
Packaging
Capsules No. 30 (No. 10x3), No. 60 (No. 10x6) in blisters in a box.
Vacation category
Without a prescription.
Producer
Limited Liability Company "Pharmaceutical Company "Zdorovya".
Location of the manufacturer and address of the place of its activity. Ukraine, 61013, Kharkiv region, Kharkiv city, Shevchenko street, building 22.
(Limited Liability Company "Pharmaceutical Company "Zdorovya")
Ukraine, 08301, Kyiv region, Boryspil city, Shevchenko street, building 100.
(Limited Liability Company "PHARMEX GROUP")
