Impaza tab. blister, 20

Storage:

active substance: 1 tablet contains affinity-purified antibodies to endothelial NO synthase: mixture of homeopathic dilutions C12, C30 and C200 – 3 mg;

excipients: lactose monohydrate, microcrystalline cellulose, magnesium stearate.

Medicinal form. Tablets.

Main physico-chemical properties: flat-cylindrical tablets, with a line and chamfer, from white to almost white in color. On one flat side, a dash is applied, on the other flat side, the inscription IMPAZA is applied.
Clinical characteristics.

Indication.

Erectile dysfunction (erectile dysfunction) of various origins.

Vegetative disorders of the climacteric period in men (weakness, fatigue, decreased physical activity, decreased libido).

Contraindication.

Increased individual sensitivity to the drug.
Use during pregnancy or breastfeeding.

Apply to adult men.

The ability to influence the speed of reaction when driving vehicles or other mechanisms.

The drug does not have a sedative effect, so it does not affect the speed of the reaction.

Method of application and dosage.

Take the drug internally. Do not use the drug together with food. Apply by
1 tablet per reception. Keep the tablet in your mouth (preferably do not chew or swallow) until completely dissolved.

Application options

1. Regular reception. To stabilize sexual potency (the ability to have sexual intercourse), a therapeutic and preventive course lasting at least 12 weeks is recommended. Depending on the severity of erectile dysfunction, the frequency of administration may vary: from 1 tablet every other day to two administrations of 1 tablet daily, preferably in the evening.
If necessary, course therapy can be repeated after 3-6 months.

2. Periodic reception. For episodic stimulation of erection, take 2 tablets 1-2 hours before intercourse before sexual intercourse.

Children.

Do not use the drug for children.

Overdose.

In case of an accidental overdose, dyspeptic manifestations caused by the components included in the composition of the drug are possible.

Adverse reactions.

Reactions of increased individual sensitivity to the components of the drug are possible.

Expiration date.

3 years.

Do not use the drug after the expiration date indicated on the package.

Storage conditions.

Store at a temperature not higher than 25 °C, in the original packaging.

Keep out of the reach of children.

Packaging.

20 tablets each in a blister made of polyvinyl chloride film and aluminum foil.

1 blister together with instructions for medical use in a cardboard box.

Leave category.

Without a prescription.

Producer.

Santonika CJSC.
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