Phosphaden tablets (Tablets, Solution) Instructions for Use
Active Substance
Adenosine phosphate (Rec.INN registered by WHO)
Clinical-Pharmacological Group
A drug that improves tissue metabolism and energy supply
Pharmacotherapeutic Group
Metabolic agent
Pharmacological Action
Adenosine phosphate (adenosine monophosphate, AMP) is a component of the most important coenzymes that regulate redox processes in the cells and tissues of the body; it is a fragment of ATP, which carries out numerous endothermic reactions that ensure muscle activity and protein synthesis.
AMP indirectly regulates the formation of aminolevulinic acid and its conversion into protoporphyrin, and plays a role in the normalization of porphyrin synthesis.
It has a vasodilating and antiplatelet effect, improves macro- and microcirculation, which, in combination with improved tissue metabolism, determines a favorable effect on tissue trophism and regeneration processes.
There is evidence of improvement in the condition of patients with psoriasis, as well as with diabetic retinopathy.
In duodenal ulcer disease, it promotes acceleration of ulcer defect healing (does not significantly affect secretory and acid-forming functions).
Pharmacokinetics
T1/2 – 10-30 sec. It is excreted by the kidneys in the form of metabolites.
Indications
Acute intermittent porphyria, polyneuritic syndrome (due to lead poisoning); acute thrombosis of superficial and deep veins of the extremities, acute arterial occlusion (during the stage of conservative treatment and in the postoperative period), obliterating endarteritis, venectomy (pre- and postoperative period), chronic venous insufficiency, thrombophlebitis, secondary vascular syndromes caused by spinal lesions.
Post-burn complications: non-healing wounds, trophic post-burn ulcers.
Hereditary diseases of the central nervous system (including hepatocerebral dystrophy – Konovalov-Wilson disease), multiple sclerosis; chronic hepatitis, liver cirrhosis, duodenal ulcer disease; coronary artery disease, chronic heart failure, asthenic syndrome, psoriasis, diabetic retinopathy.
ICD codes
| ICD-10 code | Indication |
| B18 | Chronic viral hepatitis |
| E80 | Disorders of porphyrin and bilirubin metabolism |
| E83.0 | Disorders of copper metabolism (Wilson’s disease) |
| F48.0 | Neurasthenia |
| G35 | Multiple sclerosis |
| G62.2 | Polyneuropathy induced by other toxic agents |
| H36.0 | Diabetic retinopathy |
| I20 | Angina pectoris |
| I50.0 | Congestive heart failure |
| I73.1 | Obliterative thromboangiitis [Buerger’s disease] |
| I74 | Embolism and thrombosis of arteries |
| I80 | Phlebitis and thrombophlebitis |
| I82 | Embolism and thrombosis of other veins |
| I87.2 | Venous insufficiency (chronic) (peripheral) |
| K25 | Gastric ulcer |
| K26 | Duodenal ulcer |
| K73 | Chronic hepatitis, not elsewhere classified |
| K74 | Fibrosis and cirrhosis of liver |
| L40 | Psoriasis |
| L98.4 | Chronic skin ulcer, not elsewhere classified |
| T14.1 | Open wound of unspecified body region |
| T56.0 | Lead and its compounds |
| T79.3 | Posttraumatic wound infection, not elsewhere classified |
| ICD-11 code | Indication |
| 1E51.Z | Chronic viral hepatitis, unspecified |
| 4A44.8 | Thromboangiitis obliterans |
| 5C58.Z | Congenital disorders of porphyrin and heme metabolism, unspecified |
| 5C64.0Z | Disorders of copper metabolism, unspecified |
| 6A8Z | Affective disorders, unspecified |
| 8A40.Z | Multiple sclerosis, unspecified |
| 8D43.1 | Cognitive impairments due to toxic effects |
| 8D43.2Y | Other specified neuropathy due to toxic effect |
| 9B71.0Z | Diabetic retinopathy, unspecified |
| BA40.Z | Angina pectoris, unspecified |
| BD10 | Congestive heart failure |
| BD5Z | Diseases of arteries or arterioles, unspecified |
| BD70.0 | Superficial thrombophlebitis of lower extremities |
| BD70.2 | Migratory thrombophlebitis |
| BD70.Z | Superficial thrombophlebitis, unspecified |
| BD71.4 | Deep vein thrombosis of lower extremity |
| BD74.Z | Chronic venous insufficiency of lower extremities, unspecified |
| BD7Z | Diseases of veins, unspecified |
| DA60.Z | Gastric ulcer, unspecified |
| DA63.Z | Duodenal ulcer, unspecified |
| DB93 | Fibrosis or cirrhosis of liver |
| DB97.2 | Chronic hepatitis, not elsewhere classified |
| DB98.5 | Budd-Chiari syndrome |
| EA40 | Tropical phagedenic ulcer |
| EA90.Z | Psoriasis, unspecified |
| EF60 | Ischemic ulceration of the skin |
| EM0Z | Unspecified skin disorder |
| ME60.2 | Ulcerative skin lesion of unspecified nature |
| ND56.1 | Open wound of unspecified body region |
| NE61 | Toxic effect of poisonous substances, chiefly nonmedicinal, not elsewhere classified |
| NF0A.3 | Posttraumatic wound infection, not elsewhere classified |
| BD72 | Venous thromboembolism |
| XA60H0 | Vena cava |
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 Phosphaden primarily as part of combination therapy.
For oral administration, the single dose is 25-50 mg.
For intramuscular administration, the single dose is 20-60 mg.
Adjust the frequency of administration and treatment duration based on the specific indication and disease severity.
In acute intermittent porphyria and polyneuritic syndrome, administer intramuscularly at 40-60 mg twice daily for 10-15 days.
For vascular diseases (thrombosis, thrombophlebitis, chronic venous insufficiency), use a dose of 20-40 mg intramuscularly once or twice daily; the course typically lasts 3-4 weeks.
In chronic heart failure and coronary artery disease, administer 20-40 mg intramuscularly once daily for 2-3 weeks.
For duodenal ulcer disease, use a dose of 40-60 mg intramuscularly once daily for 15-20 days.
In chronic hepatitis and liver cirrhosis, administer 40 mg intramuscularly once daily or 50 mg orally twice daily for 3-4 weeks.
For multiple sclerosis and hereditary CNS diseases, use 40-60 mg intramuscularly once daily in repeated courses.
In ophthalmic practice for conditions like diabetic retinopathy, administer via retrobulbar injections at a dose of 20 mg daily for 10-15 days.
For psoriasis and post-burn trophic ulcers, use a dose of 40-60 mg intramuscularly once daily for 20-30 days.
Repeat treatment courses if necessary, following medical supervision.
Adverse Reactions
From the cardiovascular system dizziness, tachycardia, noise in the head.
From the digestive system nausea.
Others allergic reactions are possible.
Contraindications
Hypersensitivity to adenosine phosphate.
Use in Pregnancy and Lactation
Due to rapid metabolism, it does not have any negative effect on the fetus.
Special Precautions
Intravenous administration is allowed only in a hospital setting with monitoring of cardiac activity. Administration through central veins reduces the risk of side effects.
Adenosine phosphate is not effective for atrial fibrillation, atrial flutter, or atrial extrasystole.
Drug Interactions
Dipyridamole enhances the effect of adenosine phosphate.
Xanthine derivatives (including theophylline, caffeine) reduce the effects of ATP.
Storage Conditions
Store at 2°C (36°F) to 25°C (77°F). Keep in original packaging, protected from light. Keep out of reach of children.
Dispensing Status
Rx Only
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 DisclaimerBrand (or Active Substance), Marketing Authorisation Holder, Dosage Form
Tablets 25 mg: 30 or 50 pcs.
Marketing Authorization Holder
Bivitech, LLC (Russia)
Dosage Form
| Phosphaden tablets | Tablets 25 mg: 30 or 50 pcs. |
Dosage Form, Packaging, and Composition
| Tablets | 1 tab. |
| Adenosine phosphate | 25 mg |
10 pcs. – blister packs (3) – cardboard packs.
10 pcs. – blister packs (5) – cardboard packs.
30 pcs. – dark glass jars (1) – cardboard packs.
50 pcs. – dark glass jars (1) – cardboard packs.
Tablets 50 mg: 30 or 50 pcs.
Marketing Authorization Holder
Bivitech, LLC (Russia)
Dosage Form
| Phosphaden tablets | Tablets 50 mg: 30 or 50 pcs. |
Dosage Form, Packaging, and Composition
| Tablets | 1 tab. |
| Adenosine phosphate | 50 mg |
10 pcs. – blister packs (3) – cardboard packs.
30 pcs. – dark glass jars (1) – cardboard packs.
50 pcs. – dark glass jars (1) – cardboard packs.
Tablets 25 mg: 30 or 50 pcs.
Marketing Authorization Holder
Usolye-Sibirskiy Chemical and Pharmaceutical Combine, JSC (Russia)
Dosage Form
| Phosphaden tablets | Tablets 25 mg: 30 or 50 pcs. |
Dosage Form, Packaging, and Composition
| Tablets | 1 tab. |
| Adenosine phosphate | 25 mg |
10 pcs. – blister packs (3) – cardboard packs.
10 pcs. – blister packs (5) – cardboard packs.
30 pcs. – dark glass jars (1) – cardboard packs.
50 pcs. – dark glass jars (1) – cardboard packs.
Tablets 50 mg: 30 or 50 pcs.
Marketing Authorization Holder
Usolye-Sibirskiy Chemical and Pharmaceutical Combine, JSC (Russia)
Dosage Form
| Phosphaden tablets | Tablets 50 mg: 30 or 50 pcs. |
Dosage Form, Packaging, and Composition
| Tablets | 1 tab. |
| Adenosine phosphate | 50 mg |
10 pcs. – blister packs (3) – cardboard packs.
30 pcs. – dark glass jars (1) – cardboard packs.
50 pcs. – dark glass jars (1) – cardboard packs.
Solution for intramuscular injection 20 mg/1 ml: amp. 5 or 10 pcs.
Marketing Authorization Holder
N.A. Semashko Moscow Chemical Pharmaceutical Preparations, JSC (Russia)
Dosage Form
| Phosphaden solution for injections 2% | Solution for intramuscular injection 20 mg/1 ml: amp. 5 or 10 pcs. |
Dosage Form, Packaging, and Composition
| Solution for intramuscular injection | 1 ml |
| Adenosine phosphate | 20 mg |
1 ml – ampoules (5) – blister packs.
1 ml – ampoules (10) complete with an ampoule knife or scarifier – cardboard packs.
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