Instructions for use Solidagoren oral drops 7.9 ml/10 ml bottle 50 ml
Composition
active ingredient: liquid extract from a mixture of giant goldenrod (Solidago gigantea Aiton) or Canadian goldenrod (Solidago canadensis L.), goosefoot (Potentilla anserina L.), and field horsetail (Equisetum arvense L.);
10 ml of the preparation contain 7.9 ml of liquid extract (1:1.5–2.1) from a mixture of giant goldenrod (Solidago gigantea Aiton) or Canadian goldenrod (Solidago canadensis L.), goosefoot (Potentilla anserina L.), field horsetail (Equisetum arvense L.) (4.2:1.4:1), extractant: ethanol 50% (v/v);
excipients: purified water, ethanol 96%.
Dosage form
Oral drops.
Main physicochemical properties: clear brown liquid.
Pharmacotherapeutic group
Drugs used in urology. ATX code G04B.
Pharmacological properties
Pharmacodynamics: Studies have not been conducted.
Pharmacokinetics: Studies have not been conducted.
Indication
Acute and chronic urinary tract infections (cystitis, pyelonephritis) of mild to moderate severity as part of complex therapy.
Prevention of bladder stone formation, including after their removal.
Contraindication
Hypersensitivity to the active substance or any other component of the medicinal product. Solidagoren should not be used in case of allergy to plants of the Asteraceae family, as these plants are used in the production of the herbal extract that is part of the medicinal product.
Severe heart and kidney failure, edema as a result of heart and/or kidney failure.
Interaction with other medicinal products and other types of interactions
There are no known cases of interactions with other drugs.
Due to the presence of ethanol in this medicine, it may affect the effects of other drugs.
Application features
Solidagoren is contraindicated as a diuretic for the treatment of edema caused by heart or kidney failure, especially in the elderly.
If blood appears in the urine, if the body temperature is high, or if the symptoms of the disease persist for more than 5 days, it is recommended to consult a doctor.
The medicine contains 45% (v/v) alcohol. With each intake of the recommended dose (30 drops), 0.6 g of alcohol enters the body. Therefore, this medicine is harmful for patients suffering from alcoholism. Caution should be exercised when using it in pregnant and breastfeeding women, children, patients with liver diseases and patients with epilepsy.
Use during pregnancy or breastfeeding
The medicine is not recommended for use during pregnancy or breastfeeding.
Ability to influence reaction speed when driving vehicles or other mechanisms
When following the recommended doses, it does not affect the reaction rate.
Method of administration and doses
Adults and children over 12 years of age should take 20–30 drops of Solidagoren orally with 100–200 ml of water 3 times a day. 30 drops correspond to 1.4 ml of the drug.
Fluid intake during the day when taking Solidagoren should be at least 1.5–2 liters.
The duration of use of the drug is determined by the doctor and depends on the course and severity of the disease. If the symptoms of the disease do not decrease, or any adverse reactions occur, you should stop using this drug and consult a doctor.
Children
The medicine should not be used in children under 12 years of age.
Overdose
There are no reports. In case of overdose, adverse reactions may be increased.
Side effects
Hypersensitivity and allergic reactions are very rare. Mild gastrointestinal disorders are possible (frequency unknown).
At the first signs of a hypersensitivity reaction (e.g. rash), the drug should be discontinued.
If you experience side effects not listed in the instructions, you should consult a doctor.
Expiration date
3 years.
After opening the bottle – 3 months.
Storage conditions
Store at a temperature not exceeding 25 °C.
Keep out of reach of children.
Packaging
20 ml or 50 ml or 100 ml in a bottle with a dropper; 1 bottle in a cardboard box.
Leave category.
Without a prescription.
Vacation category
Without a prescription.
Producer
Dr. Gustav Klein GmbH & Co. KG/Dr. Gustav Klein GmbH & Co. KG
