Medicines
SmPC of 29/01/2021
DIARALIA, tablet
Composition
ARSENICUM ALBUM 9 CH...................................................................................................................................1 mg
CHINA RUBRA 5 CH.............................................................................................................................................1 mg
PODOPHYLLUM PELTATUM 9 CH..........................................................................................................................1 mg
For one tablet of 300 mg
Excipients with known effect: sucrose, lactose monohydrate.
Sucrose, lactose monohydrate, magnesium stearate.
Indications
Homeopathic medicine traditionally used for the short-term treatment of acute transient diarrhoea in adults and children over 6 years of age.
Dosage and administration
Medicine reserved for adults and children over 6 years of age.
Dosage
1 tablet to be sucked, 4 to 6 times a day for a maximum treatment duration of 3 days.
Stop treatment as soon as the symptoms disappear.
Method of administration
Oral use.
Contraindications
Children under 6 years of age due to the risk of choking associated with the pharmaceutical form.
Warnings and precautions
This medicine must not be used in case of vomiting, high fever, or blood in the stools.
Any significant diarrhoea exposes to the risk of fluid and electrolyte loss requiring appropriate rehydration.
This medicine contains sucrose. Its use is not recommended in patients with fructose intolerance, glucose-galactose malabsorption syndrome or sucrase/isomaltase deficiency.
This medicinal product contains lactose. Its use is not recommended in patients with galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption syndrome (rare hereditary disorders).
Fertility, pregnancy and breastfeeding
Given the high dilutions of the strains making up DIARALIA, tablet, this medicine may be taken during pregnancy and breastfeeding.
Adverse effects
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:www.signalement-sante.gouv.fr
Pharmacodynamics
Pharmacotherapeutic class: Homeopathic medicine.
The indication for this medicine is based on the traditional homeopathic use of the preparations that make it up.
Prescription, supply and reimbursement
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Source: VIDAL · Updated on 10/11/2026. This information does not replace advice from a healthcare professional.
