Stimol®

Stimol® Instruction

stimol sq
International Non-Proprietary Name (INN)Citrulline malate
Dosage formOral solution 100 mg/1 ml: sachets 10 ml, 18 pcs.
StructureActive ingredient: citrulline malate.
Excipients: natural sangria orange flavor – 0.1 g, 30% sodium hydroxide solution – 0.1886 g, purified water – up to 10 ml.
 
10 ml – sachets made from a paper-polyethylene-aluminum complex (18) – cardboard boxes.
DescriptionOral solution in the form of a colorless or yellowish liquid with an orange scent
Pharmacological classificationGeneral tonic
ATC codeA13A
Pharmacological actionA medication used for asthenic conditions

The information presented on the instruction pages is a translation of official instructions from the manufacturers and does not reflect the opinions or views of the CosmicNootropic team. This content is provided for informational purposes only and should not be interpreted as company endorsement or opinion.

Pharmacological Action

It has an anti-asthenic effect and promotes liver detoxification.

Citrulline is an amino acid involved in the liver’s process of neutralizing ammonia, which is produced from the breakdown of nitrogen-containing compounds. In the liver, ammonia is converted into urea. Citrulline is incorporated into the urea cycle, enhancing the elimination of ammonium ions.

Malate participates in the Krebs cycle and gluconeogenesis, reducing blood lactate levels, supporting metabolic normalization, and activating the body’s non-specific defense mechanisms.

Pharmacokinetics

Absorption

After oral administration, the medication is rapidly absorbed from the gastrointestinal tract. The maximum plasma concentration (Cmax) is reached approximately 50 minutes after ingestion. It is quickly cleared from plasma, with plasma concentrations approaching physiological levels within 6 hours.

Metabolism and Excretion

Since the active component is incorporated into cellular metabolic processes, only small amounts are found in the urine.

Intended uses

Symptomatic treatment of functional asthenia:

– Asthenic syndrome

– Overwork

– Increased fatigue

– During recovery after illness

Dosage and Administration

Stimol® should be taken during meals by mixing the contents of the sachet with approximately 100 ml of plain or sweetened water.

– For adults and elderly individuals: 3.0 g (contents of 3 sachets) per day.

– For children aged 5 and older: 2.0 g (contents of 2 sachets) per day.

The course of treatment is 10-12 days. Repeat courses are possible after a break (1-3 months) or as recommended by a physician.

Side Effects

Possible: in some cases, transient abdominal pain and allergic reactions may occur at the beginning of treatment.

Contraindications

– Increased sensitivity to the medication

– Peptic ulcer disease in the acute stage

– Age under 5 years

Use During Pregnancy and Breastfeeding

The use of Stimol® during pregnancy and lactation is justified when the expected benefits outweigh the potential risks.

Use in Children

The use in children under 5 years of age is contraindicated.

Special Precautions

Each sachet contains approximately 30 mg of sodium. This should be taken into account for patients on a sodium-restricted diet.

As the formulation does not contain sugar, the medication can be prescribed to patients with diabetes mellitus.

Overdose

Data on the overdose of Stimol® are not available.

Drug Interactions

Data regarding any drug interactions with Stimol® are not available.

Storage Conditions

The medication should be stored out of reach of children at a temperature between 15°C and 25°C.

Shelf Life

The shelf life is 3 years. The medication should not be used after the expiration date indicated on the packaging.

Dispensing Conditions

The medication is available without a prescription.

Manufacturer

Biocodex, France.

Thank you!

You will now receive regular updates from us!

You’re all set!

Check your email to get your free Biohacking Guide