Nefrodol film-coated tablets 60 pieces

One tablet contains dried medicinal plants in powder form (active ingredients):

• Centaury herb (Herba Centaurii) – 18 mg;
• lovage root (Radix Levistici) – 18 mg;
• rosemary leaves (Folia Rosmarini) – 18 mg.

Excipients: corn starch; colloidal anhydrous silica; lactose, monohydrate; povidone; magnesium stearate; white sugar; hypromellose; titanium dioxide (E 171); talc; polyethylene glycol; red iron oxide (E 172); riboflavin (E 101).

• hypersensitivity to the components 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, which contain, for example, anise and fennel);
• peptic ulcer;
• edema due to heart failure or kidney dysfunction and/or a doctor’s recommendation to limit fluid intake.

Unless otherwise prescribed by a doctor, the drug should be taken by adults and children over 12 years of age, two tablets 3 times a day (total daily dose – 6 tablets).

The tablets should be swallowed without chewing, with sufficient liquid.

While taking the drug, it is necessary to ensure the consumption of sufficient amounts of fluid.

The duration of treatment is determined by the doctor individually. If the drug is well tolerated, it can be prescribed for a long period.

Pregnant women

Experience in pregnant women (300-1000 newborns) indicates no risk of fetal malformations or fetal/neonatal toxicity of Nefrodol tablets. Experimental studies have not revealed any signs of reproductive toxicity. If necessary, Nefrodol tablets can be used during pregnancy.

Due to the lack of data on the excretion of this drug or its metabolites into breast milk, a risk to the infant cannot be excluded. Therefore, it should not be used during breastfeeding.

Children

The medicine is not recommended for use in children under 12 years of age.

Drivers

The drug does not affect the ability to drive or operate other mechanisms.

Cases of drug poisoning due to overdose are unknown. Therapy is symptomatic.

Gastrointestinal disturbances (nausea, vomiting, diarrhea) are common. Allergic reactions may occur with hypersensitivity to the components of the drug, including urticaria, itching, and redness of the skin.

If any adverse reactions occur, discontinue use of the drug and consult a doctor.

Store in the original packaging at a temperature not exceeding 25 °C.

Shelf life – 4 years.