Steatel l-carnitine injection 1000 mg / 5ml box of 5 ampoules (fat burning, lean muscle, endurance, anemia, etc)


Available on backorder


Steatel l-carnitine injection 5×5 ml

pharma grade IV or IM l-carnitine with 1 gram per ampoule.

L-carnitine is used for:

  • localized fat burning in mesotherapy cocktails or main ingredient
  • athletic performance enhancement
  • improved spermatogenesis
  • improved testosterone levels
  • improved metabolism
  • recovery of muscle mass

Indications for use

Primary and secondary carnitine insufficiency in adults and children, including newborns and infants.

Secondary carnitine insufficiency in patients undergoing hemodialysis.

Secondary carnitine insufficiency suspected in patients undergoing hemodialysis in the following cases:

  • severe and persistent muscle spasms and / or hypotensive episodes of dialysis;
  • energy shortages that lead to a significant negative impact on quality of life;
  • muscle weakness and / or myopathy;
  • cardiopathy;
  • anemia not responding to erythropoietin treatment or requiring high doses of erythropoietin;
  • loss of muscle mass
  • treatment of neuropathy
  • improvement of anemia

How to use

The drug is administered intravenously slowly for 2–3 minutes.

Use in congenital metabolic disorders

During therapy, it is advisable to control the levels of carnitine and acetyl-carnitine both in the blood plasma and in the urine.

The required dose depends on the specificity of congenital metabolism and the severity of the disease.

In case of acute decompensation, the recommended dose may be up to 100 mg/kg per day for 3–4 doses. Higher doses may be used if necessary, although side effects, such as diarrhea, may be exacerbated.

Secondary carnitine deficiency in hemodialysis patients

Before starting therapy, it is advisable to monitor the level of carnitine in the blood plasma.

Secondary carnitine deficiency is diagnosed with acyl carnitine to free carnitine in the blood plasma greater than 0.4 and / or when the free carnitine concentration is less than 20 μmol/L.

A dose of 2 g should be injected intravenously at the end of each dialysis session. The overall response should be determined by monitoring the levels of acyl-carnitine and free carnitine in the blood plasma and assessing the patient’s condition. The normalization of carnitine content in muscle tissue and cardiomyocytes occurs approximately 3 months after the normal concentration of carnitine in the blood plasma is reached. If carnitine is discontinued, its level will certainly begin to decline again. The need for re-saturation treatment is determined by quantitative determination of carnitine in blood plasma at regular intervals and by monitoring the patient’s condition.

Hemodialysis is a supportive therapy

After a saturated course of intravenous levocarnitine use a maintenance dose – 1 g of the drug per day orally. On the day of dialysis, the drug is administered intravenously at a dose of 1 g immediately after the next session.

Children. The drug is used for children from the first day of life, including prematurity.


Hypersensitivity to the drug components.


Active ingredient: levocarnitine;

1 ml of solution contains 200 mg of levocarnitine – 1 gram per 5 ml.

Excipients: Hydrochloric acid, diluted, water for injection.

Release form

5 ml in a vial, 5 vials in a cardboard pack.

Storage conditions

Do not store above 25 °C in light. Keep out of the reach of children.


Help, S.A., Pedini Ioanninon, Ioannina, 45500, Greece.

Registration certificate

No48 on 11/11/2018
Registration Certificate No. UA/12945/02/01


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