Composition, form of production and packaging
? Homoeopathic drops in the form of a transparent, yellowish to reddish-yellow liquid, without a specific odor.
100 ml
hawthorn (Crataegus) D1 20 ml
arnica mountain (Arnica) D6 10 ml
potassium carbonate (Kalium carbonicum) D6 10 ml
digitalis purple (Digitalis) D12 10ml
lily of the valley May (Convallaria) D12 10 ml
Excipients: ethanol 43% by weight.
20 ml - bottles of dark glass with a dropper (1) - packs of cardboard.
50 ml - bottles of dark glass with a dropper (1) - packs of cardboard.
100 ml - bottles of dark glass with a dropper (1) - packs of cardboard.
? Tablets sublingual homeopathic round, flat-cylindrical, with a facet and a risk, almost white color with possible impregnations and marble, without a smell.
1 tab.
hawthorn (Crataegus) D1 74.8 mg
arnica mountain (Arnica) D6 37.2 mg
potassium carbonate (Kalium carbonicum) D6 37.2 mg
digitalis purpurea (Digitalis) D12 37.2 mg
lily of the valley May (Convallaria) D12 37.2 mg
Auxiliary substances: potato starch, magnesium stearate, lactose monohydrate.
12 pcs. - blisters (1) - packs of cardboard.
12 pcs. - blisters (2) - packs of cardboard.
12 pcs. - blisters (3) - packs of cardboard.
12 pcs. - blisters (4) - packs of cardboard.
INSTRUCTION FOR THE SPECIALIST.
Description of the drug approved by the manufacturer for the printed edition of 2008.
PHARMACHOLOGIC EFFECT
Complex homeopathic preparation. The hawthorn (Crataegus), arnica (Arnica), Digitalis, Convallaria, potassium carbonate increase the strength of myocardial contractions, trim the heart rate, dilate the coronary arteries, improve blood flow to the myocardium, reduce the frequency and intensity of attacks of angina pectoris .Pumpan reduces the excitability of the nervous system, has antihypertensive, antianginal and antioxidant effects, improves rheological properties of blood, microcirculation and metabolism of myocardial cells, reduces lipid peroxidation, increases diuresis.
PHARMACOKINETICS
The action of Pumpan is the result of the combined action of its components, therefore, it is not possible to carry out kinetic observations; all components can not be traced with the help of markers or bioassays. For the same reason, it is impossible to detect metabolites of the drug.
INDICATIONS
In the complex therapy with:
- IHD;
- arterial hypertension;
- chronic heart failure of stages I-II;
- Neurocirculatory dystonia.
DOSING MODE
With IHD, adults are prescribed 1 tab. or 10 drops 3 times / day. Duration of treatment - 1-2 months. At stabilization of a condition pass to supporting therapy 2 times / sut.
With arterial hypertension, adults and adolescents are prescribed 1 tab. or 10 drops 3 times / day. Duration of treatment - 2-3 months. Then support maintenance therapy is prescribed 2 times / day under the control of blood pressure.
In chronic heart failure, stage I-II, adults and adolescents are prescribed 1 tab. or 10 drops, children under 12 years - 1/2 tab. or 5 drops 3 times / day. Duration of treatment - 2-3 months. Then support maintenance therapy is prescribed 2 times / day.
With neurocirculatory dystonia, adults and adolescents are prescribed 1 tab. or 10 drops 3 times / day. Duration of treatment - 2-3 months. Then support maintenance therapy is prescribed 2 times / day.
At the onset of the disease and in cases requiring rapid relaxation of symptoms , it is possible to administer the drug to adults and adolescents for 8-10 drops,children under 12 years - 5 drops every 0.5-1 h, but no more than 8 times / day. After improving the condition, the drug is prescribed 3 times / day.
The drug is taken 30 minutes before or 1 hour after eating. Drops are taken in a pure form or diluted in 1 tablespoon of water, holding some time in the mouth before swallowing. The tablet should be kept under the tongue until it is completely resorbed.
SIDE EFFECT
Rarely: increased salivation.
The patient should be informed that if other side effects occur, you should consult a doctor.
CONTRAINDICATIONS
- alcohol addiction;
- Hypersensitivity to the components of the drug.
PREGNANCY AND LACTATION
The question of the use of Pumpan during pregnancy and lactation (breastfeeding) is decided by the doctor individually.
SPECIAL INSTRUCTIONS
Since the preparation Pumpan in the form of drops of homeopathic contains plant natural components, during storage, there may be a slight cloudiness of the solution or a decrease in odor and taste, which does not lead to a decrease in the effectiveness of the preparation.
OVERDOSE
Cases of overdose have not been registered to date.
DRUG INTERACTION
Clinically significant drug interaction between Pumpan and other drugs has not been established.
TERMS OF RELEASE FROM PHARMACY
The drug is approved for use as a means of OTC.
TERMS AND CONDITIONS OF STORAGE
The drug in the form of tablets of sublingual should be stored at a temperature of no higher than 25 В° C in a place out of the reach of children. Shelf life - 3 years. Do not use after the expiry date printed on the package.
The drug in the form of drops of homeopathic should be stored at a temperature of no higher than 25 В° C in a place protected from light and strong electromagnetic fields, inaccessible to children. Shelf life - 5 years. Do not use after the expiry date printed on the package.
