Météoxane

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Météoxane

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Medically reviewed

Marina Burgos

Last updated on 22/12/2025

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

Overview of Météoxane

Understanding Météoxane

Météoxane is a pharmaceutical preparation used to manage functional digestive disorders, particularly those characterized by intestinal gas and bloating. It is a combination medication that utilizes the properties of two active components to address gastrointestinal discomfort.

Composition and Mechanism

The efficacy of Météoxane is derived from its two primary ingredients: simethicone and phloroglucinol.

  • Simethicone: This component acts as an anti-foaming agent. It functions by altering the surface tension of gas bubbles within the digestive tract. This process causes small, trapped bubbles to coalesce into larger ones, which are then more easily eliminated through natural processes. Simethicone is chemically inert and is not absorbed into the bloodstream.
  • Phloroglucinol: This is an antispasmodic agent. It works by relaxing the smooth muscles of the intestine. By reducing muscle spasms in the gut, it helps alleviate the abdominal pain and cramping often associated with digestive transit issues.

Therapeutic Intent

Météoxane is primarily indicated for the symptomatic treatment of:

  • Intestinal Meteorism: The accumulation of gas in the gastrointestinal tract that leads to a feeling of fullness and pressure.
  • Abdominal Bloating: Visible swelling or distension of the abdominal area.
  • Functional Bowel Pain: Discomfort related to the movement and function of the digestive system without an underlying structural anomaly.

By combining a physical action on gas bubbles with a pharmacological action on muscle contractions, the medication aims to restore comfort to the digestive process.

Regulatory References

  1. Simethicone information
  2. fixed-dose combination product
  3. pharmacological class of antispasmodic and antiflatulent agents
  4. active ingredients
  5. softgel capsules

What side effects are possible with Météoxane?

Possible Side Effects and Safety Information

The official safety profile for Météoxane, a combination of Phloroglucinol and Simethicone, is structured by officially documented adverse reactions and regulatory restrictions. The majority of reported systemic adverse effects are associated with the Phloroglucinol component.


Adverse Reaction Scope

Classification Area Description
System-Organ Classes Immune system disorders and Skin and subcutaneous tissue disorders are the primary systems involved in adverse reactions.
Frequency Most systemic reactions, such as rash and urticaria (hives), are categorized as Frequency Not Known due to reporting reliance on post-marketing surveillance data.
Serious Reactions Officially documented serious adverse reactions include Anaphylactic shock and Angioedema ( Quincke's edema), which are recognized as potential, though rare, allergic events.
Exposure Pattern Acute Generalized Exanthematous Pustulosis (AGEP), a rare skin reaction, has been noted as potentially appearing at the beginning of treatment with Phloroglucinol.

Regulatory Safety Restrictions

Contraindications define situations where the medicine should not be used. Météoxane is strictly contraindicated for individuals with a known hypersensitivity to Phloroglucinol, Simethicone, or any of the product's excipients. Safety limitations also advise against use in cases of functional ileus or intestinal obstruction.

Additionally, regulatory documents note a specific incompatibility between Phloroglucinol and morphine-class analgesics because of the potential for the opioid to counteract the spasmolytic effect of the Phloroglucinol component.


Safety Profile Summary

The safety profile emphasizes the potential for systemic allergic reactions as the principal risk. The documented restrictions concerning hypersensitivity and morphine-class analgesics establish the main regulatory safety boundaries for the use of this medicine.

Overdose and Emergency Response

Overdose and when to seek help

The official regulatory documentation for Météoxane indicates a distinct lack of specific, defined toxicological outcomes in the event of an overdose. Regulatory summaries for the active component Phloroglucinol note that reported cases of overdose have been described as occurring without any specific symptomatology. Furthermore, regulators confirm that no cases of overdose have been reported in the labeling for the Simethicone component. No severe or life-threatening outcomes are formally documented in the overdose sections of official prescribing information.


Emergency Action Required

Due to this absence of specific toxicological data, regulatory authorities mandate that patients must contact their nearest hospital casualty department or tell their doctor immediately if they have taken more than the labeled amount. Urgent medical attention is required for any suspected overdose to allow for a comprehensive professional assessment.


Management and Supportive Measures

Overdose management is limited to symptomatic and supportive treatment. The official prescribing information states that no specific antidote is known or specified to counteract the effects of an overdose of either active substance. Treatment may involve the administration of fluids and observation, aligning with the general regulatory standards for non-systemic substances.

Therapeutic Uses of Météoxane

Quick Facts

  • Targeted Use: Symptomatic relief for certain functional digestive discomforts.
  • Key Relief Area: Helps manage abdominal pain and bloating.
  • Associated Conditions: Used when abdominal symptoms are accompanied by gas or mild diarrhea.

What Météoxane treats: main uses and benefits

Météoxane is a medication intended for the symptomatic management of certain digestive discomforts. Its primary use is in providing relief from abdominal pain that is linked to a sensation of fullness or gas in the digestive tract. The treatment may be employed when these discomforts include gas emissions, bloating, and may also be associated with mild diarrhea.

The medication is primarily indicated for addressing the functional manifestations of these intestinal disorders. As a treatment, Météoxane works to help reduce the digestive contractions (spasms) that may contribute to the pain. It also functions to help decrease the formation of intestinal gas that results in bloating. The therapeutic aim is to help relieve the primary symptoms and promote overall digestive comfort.

This medication is a component of the supportive treatment approach for functional bowel disorders, where the management goal is the reduction of pain and the normalization of transit, often in conjunction with lifestyle and dietary adjustments.

Eligibility and Restrictions for Use

Eligibility: Who Can and Cannot Use Météoxane?

Météoxane is a combination medicine whose official eligibility profile is defined by the regulatory rules for its active ingredients, Phloroglucinol and Simethicone. The medicine is primarily indicated for use in adults and children over 2 years of age.

Use of Météoxane is contraindicated in several population groups. Patients must not use this medicine if they have a known hypersensitivity or allergy to Phloroglucinol, Simethicone, or any excipients in the product. It is also formally excluded for individuals with pre-existing gastrointestinal conditions such as Intestinal Obstruction or Functional Ileus.

Regulatory authorities also place specific restrictions on its use in special populations.

Population Group Eligibility Status
Children under 2 years Not Recommended (Efficacy not established)
Pregnant women Restricted/Conditional Use (Only when strictly necessary and advised by a physician)
Breastfeeding women Avoided (Not recommended due to insufficient data)

Eligibility is also affected by certain rare hereditary conditions linked to excipients, such as Phenylketonuria, if the specific formulation contains the relevant substance.

What should I know about interactions with other medicines?

Interactions with other medicines and products

The interaction profile for Météoxane, which contains Phloroglucinol and Simethicone, is based primarily on the known properties of its active ingredients as outlined in official regulatory and authoritative biomedical sources.

Simethicone Component Interactions

Simethicone is generally considered physiologically inert and is not systemically absorbed from the gastrointestinal tract. Consequently, official documentation suggests a limited risk for traditional pharmacokinetic drug-drug interactions (involving absorption, metabolism, or excretion).

However, authoritative sources have documented one specific pharmacokinetic interaction:

  • Thyroid Hormone Preparations (e.g., Levothyroxine, Liothyronine): Simethicone may potentially interfere with the absorption of these agents when co-administered. To mitigate the risk of reduced therapeutic effect of the thyroid medicine, the official recommendation is to separate the administration of the simethicone-containing product from the thyroid hormone by at least a four-hour interval.

Phloroglucinol Component Interactions

Official regulatory documentation for Phloroglucinol-containing products states a specific pharmacodynamic interaction related to its mechanism of action as a spasmolytic agent:

  • Major Analgesics (e.g., Morphine or Morphine Derivatives): The concomitant use of Phloroglucinol with these analgesic classes is officially discouraged due to their spasmogenic (spasm-inducing) effects, which may counteract or inhibit the smooth-muscle relaxing effect of Phloroglucinol. This represents an antagonism of pharmacologic effect.

Summary of Constraints

The regulatory structure emphasizes two key constraints: a time-separation requirement for certain narrow-therapeutic-index drugs (thyroid hormones) and a do-not-combine constraint with major spasmogenic analgesics to prevent therapeutic failure.

Mechanism of Action

The action of Météoxane is driven by a dual, complementary mechanism that influences two distinct factors in the digestive tract: smooth muscle hypercontractility and entrapped gas.


Modulation of Gastrointestinal Smooth Muscle Tone

The spasmolytic component, Phloroglucinol, exerts a direct musculotropic action by engaging key molecular targets within the smooth muscle cells of the digestive system. Its primary focus is the inhibition of voltage-dependent calcium channels and specific Phosphodiesterase (PDE) enzymes. By suppressing calcium influx and modulating the cAMP/cGMP pathway, this mechanism causes the relaxation of hypercontractile muscle tissue. This mechanism produces a reduction in excessive gut wall tension and aberrant muscle activity.


Physical Alteration of Intestinal Gas

The antiflatulent component, Simethicone, operates via a local physical mechanism as a non-systemic surfactant. It targets the surface tension of the numerous small gas bubbles and foam films trapped within the intestinal contents. By reducing surface tension, Simethicone facilitates the coalescence of these tiny, resilient bubbles into larger, more easily managed gas pockets. This physical change facilitates the elimination of intraluminal gas, a process that alters the mechanical state of the abdomen by resolving the trapped gas volume.

Dosage and Administration Information

Official Administration Instructions

Météoxane is a combination medicine containing phloroglucinol and simethicone, formulated as capsules for oral use. The instructions for administration define the procedural steps, dosage, and timing of the medicine.

Administration Element Official Rule
Route of Administration Oral route (swallowed).
Standard Adult Dose Two (2) capsules per dose.
Frequency Three times a day (3 times/day).
Timing Before meals or at the time of pain.

Procedural Structure

To use this medication, it is specified that the capsules should be swallowed whole with a small amount of water. The maximum daily dose for adults should generally not exceed six capsules. The administration is structured as an 'as-needed' regimen linked to a maximum frequency, allowing flexibility based on symptoms while maintaining a safety ceiling.

Special Conditions

The instructions specify that the medicine should be taken at a particular time relative to food (before meals) or in response to a specific condition (at the time of pain). If the maximum dose of six capsules per day is insufficient to achieve relief, or if symptoms persist, the patient is advised to consult a physician. There are no specific preparation steps, such as shaking or dilution, documented for the capsule form.

Recent Clinical Evidence

Météoxane: Recent Clinical Evidence


Evidence for Use in Functional Digestive Symptoms

Research evaluating Météoxane was studied for its authorized use in functional intestinal manifestations, including abdominal discomfort, cramping, and symptoms related to excess gas (meteorism). The primary evidence relies on Randomized Controlled Trials (RCTs) and systematic reviews. Studies explored changes in patient-reported outcomes such as the severity and frequency of abdominal pain, cramping, and bloating in adult populations. For the antispasmodic component, systematic reviews indicate that findings were mixed across some older trials. Research on the antiflatulent component contributed to the broader evidence landscape concerning the study of the component for gas-related symptoms. Evidence is limited for the specific fixed-dose combination in large-scale, contemporary RCTs across the full spectrum of target symptoms.

Research Gaps and Limitations

Clinical trials for Météoxane and its core components are relevant in trials assessing short-term or episodic symptom patterns. Follow-up durations were limited to just a few weeks in most key efficacy trials, meaning long-term effects are not fully established. Data for certain groups remain insufficient, particularly for older adults with multiple health conditions and for use in children or adolescents, as the core efficacy research was evaluated in primarily adult populations. The overall evidence base has noted specific limitations, including modest sample sizes and the absence of a large number of direct RCTs assessing the combination against placebo.

Key Studies & References

  1. Simethicone for the treatment of upper gastrointestinal diseases: systematic review and meta-analysis

Frequently Asked Questions (FAQ)

Common questions about Météoxane (FAQ)

Q: What is Météoxane used for?

Météoxane is used to treat bloating and abdominal distension related to gas accumulation in the intestines. It is often prescribed for individuals experiencing discomfort and swelling due to excessive intestinal gas.

Q: What are the main ingredients in Météoxane?

Météoxane contains two main active substances:

  • Phloroglucinol: This ingredient helps to relax the smooth muscles of the digestive and urinary tracts, which can help relieve spasms associated with pain and discomfort.
  • Simeticone: This ingredient is an anti-foaming agent that works in the stomach and intestines to break up gas bubbles, making them easier to pass and reducing bloating.

Q: Can Météoxane be taken with other medications?

It is important to discuss all medications and supplements you are taking with your doctor or pharmacist before starting Météoxane. While no known major interactions are widely reported, professional advice ensures safe use, especially regarding absorption or effect on other digestive system treatments.

Q: How long does it take for Météoxane to work?

The time Météoxane takes to work can vary among individuals. The simeticone component typically begins to act quickly by breaking down gas bubbles soon after ingestion. Relief from symptoms of bloating and gas may be noticeable within a relatively short period, often within hours of taking the first dose. However, consistent use as directed may be needed for full symptom management.

Q: What should I do if I forget to take a dose of Météoxane?

If you forget to take a dose, take it as soon as you remember. However, if it is almost time for your next scheduled dose, skip the missed dose and continue with your regular dosing schedule. Do not double the dose to make up for a missed one. If you are unsure, consult your pharmacist or doctor.

How should Météoxane be stored and disposed of?

How to Store and Dispose of Météoxane?

Storage Requirements

Météoxane soft capsules do not require any special storage conditions to remain stable throughout their documented shelf life of 3 years. The medicine must, however, be kept out of the sight and reach of children to prevent accidental ingestion, as required by official labeling.

Disposal Instructions

Official regulations prohibit the disposal of Météoxane via wastewater or household waste. This measure is mandatory to help protect the environment.

To discard unused or expired capsules properly, the medicine must be returned to a pharmacy or local waste disposal company authorized to handle pharmaceutical waste. This ensures safe and appropriate environmental handling.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

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