Instructions Resistol oral drops 800 mg/g bottle with dropper stopper 50 ml
Composition
active ingredient: 1 g of solution contains pelargonium root liquid extract (Pelargonii radix extractum liquidum) (extractants: ethanol 40% (v/v), ethanol 10% (v/v)) (1:8-10) 800 mg;
excipient: glycerin 85%.
Dosage form
Oral drops.
Main physical and chemical properties: liquid from light brown to red-brown in color. During storage, sediment and turbidity may occur.
Pharmacotherapeutic group
Medicines used for coughs and colds. ATX code R05.
Pharmacological properties
Pharmacodynamics
The drug contains an extract of Pelargonium sidoides roots.
The drug affects the mechanism of attachment of bacteria and viruses to the mucous membrane, thereby preventing the penetration of viruses and bacteria into the body. The drug has a pronounced immunomodulatory effect, which causes rapid suppression of viral infection. It also prevents the reproduction of bacteria that have already penetrated the body, thereby preventing the development of complications. The drug helps to activate the mechanisms of cleansing the respiratory tract, which improves the removal of viscous mucus and eliminates the conditions for further reproduction of pathogenic bacteria.
Treatment with the drug leads to rapid relief of symptoms such as cough, heavy sputum discharge, general malaise, fever, and runny nose, significantly shortens the duration of the disease, and inhibits the development of resistance in microorganisms.
The drug is a complex mixture of many components, which as a whole is considered an active substance.
Pharmacokinetics
There are no data on the pharmacokinetics of the drug.
Indication
Acute and chronic infections of the respiratory tract and nasopharynx (bronchitis, sinusitis, tonsillar angina, rhinopharyngitis).
Contraindication
Hypersensitivity to any ingredient of the drug, tendency to bleeding, simultaneous administration of drugs that slow down the blood clotting process, severe liver or kidney diseases (due to lack of sufficient experience with the use of this drug in such cases).
Special safety measures.
Resistol® contains 12 vol. % ethanol.
Interaction with other medicinal products and other types of interactions
There are no reports of interactions. Due to the possible effect of Resistol® on blood coagulation parameters, it cannot be ruled out that when used simultaneously with coumarin derivatives or other drugs that prevent blood clotting, their anticoagulant effect may be enhanced. No interactions of Resistol® with penicillin V have been identified.
Use during pregnancy or breastfeeding
Due to the lack of sufficient experience with the use of Resistol® in pregnant and breastfeeding women, it should not be used during pregnancy and breastfeeding.
Ability to influence reaction speed when driving vehicles or other mechanisms
The effect of the drug on the reaction rate when driving vehicles or other mechanisms has not been studied, but it should be noted that the drug contains 12 vol. % ethanol.
Method of administration and doses
Adults and children over 12 years of age: 30 drops 3 times a day.
Children aged 6 to 12 years: 20 drops 3 times a day.
Children aged 1 to 6 years: 10 drops 3 times a day.
The solution should be used with a small amount of liquid in the morning, afternoon and evening.
Hold the bottle vertically, if necessary, tap the bottom lightly.
After the symptoms of the disease subside, it is recommended to continue treatment with Resistol® for several more days to prevent relapse. The total duration of treatment should not exceed three weeks.
Children
Due to the lack of sufficient data on the use of the drug in infants, Resistol® should not be used in children under 1 year of age. The use of Resistol® for the treatment of young children (from 1 to 6 years) is recommended under the supervision of a physician.
Overdose
There are no reports of overdose. Possible increase in adverse reactions.
Adverse reactions
On the part of the digestive tract: digestive tract disorders (including stomach pain, heartburn, nausea, diarrhea), mild bleeding gums.
Respiratory system: mild nosebleeds.
Skin/immune system disorders: hypersensitivity reactions (including skin rash, urticaria, itching of the skin and mucous membranes). In extremely rare cases, severe hypersensitivity reactions with facial swelling, shortness of breath and a decrease in blood pressure are possible.
Hepatobiliary system: increased liver function tests. A causal relationship between the increase in these tests and the use of the drug has not been demonstrated.
Expiration date
2 years.
The shelf life after opening the package is 3 months.
Storage conditions
Store in original packaging at a temperature not exceeding 25 0C.
Keep out of reach of children.
Packaging
20 ml or 50 ml in a bottle closed with a dropper stopper and a tamper-evident cap; 1 bottle in a pack.
Vacation category
Without a prescription.
Producer
PJSC "Halychpharm".
Location of the manufacturer and address of its place of business
Ukraine, 79024, Lviv, Opryshkivska St., 6/8.
