OLIGOSOL Manganese Cobalt Oral solution in ampoule 28Amp/2ml

Oral solution.
Ampoule with two self-breaking tips of 2 ml. Box of 28.

For one ampoule of 2 ml:

Manganese gluconate: 0,590 mg
(Corresponding quantity of manganese: 0,0728 mg)

Cobalt gluconate: 0,553 mg
(Corresponding quantity of cobalt: 0,0726 mg)

Excipient with known effect: glucose (100 mg in one ampoule of 2 ml).

Used as a terrain modifier, particularly during states of neurovegetative dystonia.

Dosage

FOR ADULTS ONLY.

1 to 2 ampoules per day.

The ampoules are to be taken:

• preferably in the morning on an empty stomach,
• possibly 15 minutes before a meal or in the evening at bedtime.

Method of administration

Oral use.

Sublingual administration is recommended: hold the contents of the ampoule under the tongue for 1 to 2 minutes before swallowing.

Hypersensitivity to the active substances or to any of the excipients listed in section Composition.

This medicine contains glucose. Its use is not recommended in patients with glucose-galactose malabsorption syndrome.

The data available to date do not suggest the existence of clinically significant interactions.

In the absence of experimental and clinical data, and as a precaution, use of this medicine should be avoided during pregnancy and breastfeeding.

Reporting of suspected adverse reactions

Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the national reporting system: National Agency for the Safety of Medicines and Health Products (ANSM) and the network of Regional Pharmacovigilance Centres - Website: https://signalement.social-sante.gouv.fr.

No cases of overdose have been reported.

Pharmacotherapeutic class: OLIGOTHERAPY (V: various)

Trace mineral elements.

5 years.

Store at a temperature below 25 °C.

No special requirements.