

Novo-Passit is a combined phytopreparation with a sedative effect, the pharmacological activity is due to its constituent components of the extract based on medicinal raw materials with a predominantly sedative effect and guaifenesin, which has an anxiolytic effect. The sedative effect of the drug is supplemented by the anxiolytic effect of guaifenesin.
Neurasthenia and neurotic reactions, accompanied by irritability, anxiety, fear, fatigue, distraction; manager's syndrome (state of constant mental stress); insomnia (mild forms); headaches caused by nervous tension, migraine, functional diseases of the gastrointestinal tract (dyspeptic syndrome, irritable bowel syndrome), menopausal syndrome, neurocirculatory dystonia, pruritic dermatosis (atopic and seborrheic eczema, urticaria) caused by psychological stress.
1 tab. contains dry extract of medicinal plants: Valeriana officinalis, Melissa officinalis, St. John's wort, St. John's wort, Passionflower Incarnate (passionflower), common hops, black elderberry) 0.1575 g, Guaifenesin 0.200 g;
excipients: core - colloidal silica; MCC; Compritol "888 ATO" magnesium stearate; lactose "Fast flow" shell - opadri "AMB 80W31115" green.
Novo-Passit® is marketed under different brands and generic names, and comes in different dosage forms:
Brand name | Manufacturer | Country | Dosage form |
---|---|---|---|
Novo Passit | Teva | Israel | pills |
Novo Passit | Teva | Israel | solution |
Novo Passit | Teva | Czech | pills |
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Novo-Passit is taken orally, for adults and children over 12 years old - 5 ml each (1 tsp) or 1 tab. 3 times a day. If necessary, the daily dose can be increased to 10 mg or 2 table. 3 times a day. The dose can be changed depending on the response of the patient.
The drug can be taken with drinks (tea, juice). In case of nausea, the drug should be taken with food. Since the recommended doses of the drug usually does not cause drowsiness and loss of attention, it can be taken in the daytime.
For children under 12 years old, use only as directed by a doctor! The dose is selected individually, taking into account age and tolerability. The recommended initial dose is 1/2 tsp. Or 1/2 tbl. a day before bed.
In rare cases, possible: dizziness, lethargy, fatigue, drowsiness, allergic reactions, exanthema, decreased concentration; gastrointestinal disorders (nausea, vomiting, cramping, heartburn, diarrhea, constipation).
Hypersensitivity to the drug components, myasthenia gravis, children under 12 years old.
The drug should be used with caution in patients with acute gastrointestinal diseases, liver diseases, chronic alcoholism, diseases and injuries of the brain, and epilepsy.
While taking the drug Novo-Passit® and other drugs their action may be enhanced or weakened. Before you start taking the drug at the same time as other drugs, you should consult with your doctor.
The drug enhances the effect of alcohol and other substances that depress the central nervous system.
Drugs used to relax skeletal muscles (central muscle relaxation) can increase the risk of side effects of the drug, first of all - muscle weakness.
Hypericum extract contained in the preparation reduces the effectiveness of hormonal contraception, as well as drugs used mainly after transplantation to reduce the risk of rejection of a transplanted organ or tissue (immunosuppressive drugs), drugs intended for the treatment of AIDS, cardiovascular diseases, bronchial diseases and prevention of thromboembolism . Therefore, before you start taking Novo-Passit® against the background of these drugs must consult a doctor.
During pregnancy, especially during the first trimester, and during breastfeeding, you should consult with your doctor.
The drug contains 12.19% ethanol; each single dose contains up to 0.481 g of ethanol. During treatment with the drug should not consume alcoholic beverages.
During the reception of Novo-Passit, especially for patients with fair skin, exposure to ultraviolet radiation should be avoided (prolonged exposure to direct sunlight, visiting a tanning bed).
When taking the drug should not drive vehicles and mechanisms. The drug is not recommended for patients with impaired glucose and galactose digestibility and with congenital fructose intolerance.
If within 7 days the symptoms of the disease do not disappear, or their aggravation occurs, as well as in the event of side effects or other unusual reactions, it is recommended to consult a doctor.
Instructions for diabetics: 100 g of the drug contains 12.5-14.2 g of glucose and 13.6-15.3 g of fructose. When taken in recommended doses, each dose contains not more than 1.42 g of glucose and 1.53 g of fructose.
Overdosing is first manifested by a feeling of depression and drowsiness. Later, these symptoms may be accompanied by nausea, mild muscle weakness, pain in the joints, and a feeling of heaviness in the stomach. If you have symptoms of overdose, the drug should be discontinued. Symptomatic treatment. It is necessary to consult a doctor.