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Dosage form: & nbspextract liquid for oral administration
Composition:

Per 1000 ml of the preparation

Active substances:

St. John's wort 8,0 g, dandelion of medicinal roots 8,0 g, immortelle of sandy flower 7,0 g, senna leaves 7,0 g, thyme grass 2,0 g, rhodiola of pink rhizome and roots 0,1 g.

Excipient: Ethanol (ethyl alcohol) 38-45% - sufficient amount to obtain 1000 ml of the drug.

Description:The liquid is from yellowish brown to dark brown with a characteristic odor; in the course of storage, a slight precipitate may fall out.
Pharmacotherapeutic group:Generalizing agent of plant origin
Pharmacodynamics:

It has antioxidant, detoxifying and restorative effect, caused by a complex of biologically active substances that make up a medicinal plant preparation. In clinical studies, the use of the drug in weakened patients led to an increase in appetite, improvement in general condition and increase in ability to work; At the same time, the normalization of the state of the neutrophilic link of immunity and peripheral blood parameters was noted.

Indications:As part of complex therapy in adult patients with asthenic conditions,in the period of convalescence after severe diseases, in the postoperative period, with physical and mental overwork.
Contraindications:

Hypersensitivity to the components of the drug, acute period of infectious diseases, cholelithiasis, gastritis during exacerbation, acute pancreatitis, peptic ulcer of the stomach and duodenum during an exacerbation, liver disease, alcoholism, traumatic brain injury, brain diseases, pregnancy, breastfeeding, age to 18 years.

Pregnancy and lactation:Contraindicated use of the drug during pregnancy and during breastfeeding.
Dosing and Administration:

Inside, 15 ml (1 tablespoon) of the drug, previously diluted in 100 ml of boiled water, 3 times a day after meals. The course of treatment is 3-4 weeks.

Side effects:

Possible allergic reactions, photosensitizing effect (increased sensitivity of the skin to the action of sunlight).

If any of the side effects listed in the manual are aggravated, or if you notice any other side effects not listed in the instructions, tell your doctor.

Overdose:

Symptoms of an overdose: impaired coordination of movements, drowsiness, anxiety, irritability, nausea, vomiting, tachycardia, dizziness, confusion; with severe overdose - convulsions, hallucinations, sweating, delirium, coma, slowing or stopping breathing, lowering body temperature, stopping the heart.

Treatment: with mild overdose - gastric lavage followed by activated charcoal; when severe alcohol poisoning - treatment in a hospital.

Interaction:

With the joint application of St. John's Wort preparations with warfarin, digoxin, cyclosporine, steroid drugs, antiviral (HIV) agents (amprenavir, indinavir, nevirapine, nelfinavir, ritonavir, saquinavir, efavirenz) may reduce their effectiveness. The use of the drug may enhance the photosensitizing effect of other drugs, including piroxicam, sulfonamides, tetracyclines, thiazide diuretics, quinolones.

It is possible to increase the antidepressant effect of monoamine oxidase inhibitors, with an increased risk of their side effects.When combined with fluoxetine, paroxetine, sertraline, fluvoxamine or citalopram, weighting of the hemolytic

reactions and the course of "serotonin syndrome" (dizziness, nausea, vomiting, headache, epigastric pain, anxiety, confusion, confusion, anxiety and irritability). It is possible to reduce the hypotensive effect of reserpine and the concentration of cyclosporine in the blood. When used concomitantly with ethinylestradiol and desogestrel, the risk of bleeding may increase. It is possible to accelerate the metabolism of theophylline.

Special instructions:

Before you start taking the drug is recommended to consult a doctor.

The content of ethyl alcohol in the preparation is 38-45%.

In the maximum single dose (15 ml) of the drug contains up to 5.33 grams of absolute ethyl alcohol, the maximum daily dose (45 ml) of the drug contains up to 15.98 grams of absolute ethyl alcohol.

Effect on the ability to drive transp. cf. and fur:

During the period of drug use, one should refrain from carrying out potentially dangerous activities requiring an increased concentration of attention and speed of psychomotor reactions (managementvehicles, work with moving mechanisms, the work of a dispatcher, an operator).

Form release / dosage:

Extract liquid for oral administration.

Packaging:

To 50 ml, 100 ml in bottles of dark glass with a screw mouth, ukuporennyh caps aluminum with perforation. Each bottle together with the instruction for use is placed in a pack of cardboard box.

Storage conditions:

In the dark place at a temperature of 15 to 25 ° C.

Keep out of the reach of children.

Shelf life:

2 years.

Do not use after the expiration date.

Terms of leave from pharmacies:Without recipe
Registration number:LP-004267
Date of registration:28.04.2017
Expiration Date:28.04.2022
The owner of the registration certificate:FITOGALENIKA, LLCFITOGALENIKA, LLC Russia
Manufacturer: & nbsp
Information update date: & nbsp02.06.2017
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