Doppelherz® Cardiovital (Tablets) Instructions for Use
Marketing Authorization Holder
Queisser Pharma, GmbH & Co. KG (Germany)
ATC Code
C01EB04 (Hawthorn glycosides)
Active Substance
Crataegi folium cum flore (DAB German Pharmacopoeia)
Dosage Form
| Doppelherz® Cardiovital | Coated tablets, 300 mg: 20, 30, or 50 pcs. |
Dosage Form, Packaging, and Composition
Coated tablets, brown in color with dark specks, round, biconvex; the coating is transparent.
| 1 tab. | |
| Dry extract of hawthorn leaves with flowers | 300 mg |
Excipients: lactose monohydrate, powdered cellulose, highly dispersed silicon dioxide, copovidone, high-chain glycerides, povidone, corn starch, sodium croscarmellose, talc, magnesium stearate.
Coating composition: shellac, methacrylic acid-ethyl acrylate copolymer (1:1), sodium dodecyl sulfate, polysorbate 80, macrogol 6000, talc, simethicone emulsion.
10 pcs. – blisters (2) – cardboard packs.
10 pcs. – blisters (3) – cardboard packs.
10 pcs. – blisters (5) – cardboard packs.
Clinical-Pharmacological Group
Herbal preparation used for heart failure
Pharmacotherapeutic Group
Cardiotonic agent of plant origin
Pharmacological Action
A cardiotonic agent of plant origin. It has a moderate cardiotonic effect, improving the function of the heart muscle.
It possesses spasmolytic properties. By selectively dilating the coronary vessels and cerebral vessels, it exerts a hypotensive effect and helps normalize venous pressure.
It exhibits sedative properties.
Pharmacokinetics
Data on the pharmacokinetics of the drug Doppelherz® Cardiovital are not provided.
Indications
- As part of complex therapy for chronic heart failure of functional classes I and II according to the NYHA classification.
ICD codes
| ICD-10 code | Indication |
| I50.0 | Congestive heart failure |
| ICD-11 code | Indication |
| BD10 | Congestive heart failure |
Dosage Regimen
| The method of application and dosage regimen for a specific drug depend on its form of release and other factors. The optimal dosage regimen is determined by the doctor. It is necessary to strictly adhere to the compliance of the dosage form of a specific drug with the indications for use and dosage regimen. |
Administer orally with a sufficient amount of liquid. The standard dosage is one tablet taken two to three times daily.
The typical duration of a treatment course is six weeks. Conduct subsequent courses if deemed necessary by a physician based on clinical evaluation.
Adverse Reactions
Observe for adverse reactions primarily from the cardiovascular system and skin. With prolonged use at high doses, bradycardia and arterial hypotension may occur.
Monitor for potential allergic reactions, including urticaria and pruritus. Discontinue use immediately if signs of hypersensitivity appear.
Drug Interactions
Exercise caution with concomitant use of cardiac glycosides, such as digoxin or strophanthin. A pharmacodynamic interaction leads to an additive inotropic effect on the heart muscle.
Consider potential interactions with antihypertensive agents and central nervous system depressants due to the drug’s own hypotensive and mild sedative properties. Monitor for enhanced effects.
Contraindications
- Do not use in patients with a known hypersensitivity to the active substance, hawthorn, or any of the excipients listed in the composition.
- This product is contraindicated during pregnancy due to a lack of sufficient safety data.
- Avoid use throughout the entire period of lactation (breastfeeding).
- Do not administer to children or adolescents under 18 years of age as safety and efficacy have not been established in this population.
Overdose
No specific cases of overdose have been reported to date. Given the pharmacological profile, symptoms of severe overdose could theoretically include pronounced bradycardia and a significant drop in blood pressure.
In case of suspected overdose, immediately discontinue the medication and initiate symptomatic and supportive care. There is no known specific antidote.
Use in Pregnancy and Lactation
The drug Doppelherz® Cardiovital is contraindicated for use during pregnancy and the breastfeeding period.
Storage Conditions
The drug should be stored in a dry place, out of the reach of children, at a temperature not exceeding 25°C (77°F).
Shelf Life
Shelf life – 3 years.
Dispensing Status
The drug is dispensed by prescription.
Important Safety Information
This information is for educational purposes only and does not replace professional medical advice. Always consult your doctor before use. Dosage and side effects may vary. Use only as prescribed.
Medical Disclaimer
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