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Kalium phosphoricum (Granules) Instructions for Use

Marketing Authorization Holder

Boiron (France)

Contact Information

Boiron (France)

ATC Code

V30 (Not assigned)

Dosage Forms

Bottle OTC Icon Kalium phosphoricum Homeopathic granules C5: 4 g tube with granule counter
Homeopathic granules C9: 4 g tube with granule counter
Homeopathic granules C15: 4 g tube with granule counter
Homeopathic granules C30: 4 g tube with granule counter

Dosage Form, Packaging, and Product Composition

Homeopathic granules Potency
Kalium phosphoricum (Kalium phosphoricum) C5
Homeopathic granules Potency
Kalium phosphoricum (Kalium phosphoricum) C9
Homeopathic granules Potency
Kalium phosphoricum (Kalium phosphoricum) C15
Homeopathic granules Potency
Kalium phosphoricum (Kalium phosphoricum) C30

Excipients : sucrose, lactose.

4 g – tubes with granule counter (1) – cardboard packs.

Clinical-Pharmacological Group

Single-component homeopathic preparation of mineral-chemical origin

Pharmacotherapeutic Group

Homeopathic agent

Pharmacological Action

Kalium phosphoricum (dipotassium phosphate) is a white powder that is easily soluble in water but poorly soluble in alcohol.

Like other potassium salts, it is present in nerve tissues, in muscle tissue cells, and in blood cells (primarily in red blood cells).

Indications

Administer for the symptomatic management of conditions characterized by specific physical and mental manifestations of asthenia.

  • Use for physical and mental asthenia resulting from overexertion or during recovery from infectious diseases.
  • Employ for associated symptoms including headaches, dizziness, memory impairment, and insomnia, which may be accompanied by night terrors or sleepwalking.
  • Indicated for asthenia related to sexual disorders and for normocytic anemia.
  • Presence of key guiding symptoms such as increased sensitivity to sound and touch, heaviness or pain in the occiput, a sensation of a lump in the throat, or an empty stomach sensation relieved by eating supports use.

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 sublingually by allowing the granules to dissolve completely in the mouth.

Take doses 30 minutes before or 60 minutes after a meal to ensure optimal absorption. For infants and children from 0 to 3 years of age, first dissolve the granules by shaking them in 10-15 ml of room temperature water and administer the entire solution.

The standard and optimal single dose is 5 granules. A healthcare professional must determine the appropriate homeopathic potency (C5, C9, C15, C30), dosing frequency, and total duration of treatment based on individual patient presentation and response.

Adverse Reactions

No adverse reactions have been reported or described for this preparation to date.

Due to the high dilution of the active substance characteristic of homeopathic products, the risk of adverse effects is considered minimal. Despite this, remain vigilant for any unusual symptoms following administration and report them to a healthcare provider.

Contraindications

Do not administer this drug to patients with known hypersensitivity to any of its components.

  • Contraindicated in individuals with a history of hypersensitivity or idiosyncratic reaction to the drug itself.
  • Strictly avoid use in patients with lactose intolerance, as the granules contain lactose as an excipient.

Special Precautions

The dosage regimen and frequency of administration are determined by the doctor.

If there is no therapeutic effect within 3 days, or if adverse reactions occur, you should consult a doctor.

Overdose

No cases of overdose have been reported, and due to the nature of homeopathic dilutions, toxic effects from the active ingredient are not expected.

In the event of accidental ingestion of a significantly larger number of granules than prescribed, the primary risk is related to the excipients (sucrose, lactose). Monitor for gastrointestinal discomfort. Initiate symptomatic and supportive care if necessary.

Drug Interactions

No clinically significant drug interactions are known or expected.

The use of other medicinal products, including conventional allopathic treatments, is permitted concurrently. The high dilution of the active substance minimizes the potential for pharmacological interference. Continue all other prescribed medications unless specifically instructed otherwise by a physician.

Storage Conditions

At a temperature not exceeding 25°C (77°F).

Shelf Life

Shelf life – 5 years.

Dispensing Status

The drug is available without a 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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