Reisziekte

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Reisziekte

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Overview of Reisziekte

What is Reisziekte? Defining the Antiemetic Entity

Property Description
Active ingredient Cyclizine (as the hydrochloride salt)
Form Tablet, Capsule, Suppository
Pharmacological class H₁-receptor antagonist, Antiemetic
Common use Prevention and relief of motion sickness (Kinetosis)
Origin Synthetic (Piperazine derivative)

The term Reisziekte is the specific Dutch nomenclature for a medication designed for the symptomatic treatment of motion sickness, or kinetosis. This preparation is therapeutically classified as an antiemetic, primarily functioning through its membership in the first-generation histamine H₁-receptor antagonist class, or H₁-blockers. The core function of this substance is to counter the distressing symptoms of travel, notably nausea, vomiting, and dizziness, a benefit that is clinically recognized. The primary conclusion derived from this classification is that the medication works by directly targeting the body's motion and balance signaling systems, providing effective relief during typical travel scenarios, such as extended car journeys or sea voyages.

The effectiveness of the medication hinges on its active ingredient, Cyclizine, which is a synthetic compound classified chemically as a piperazine derivative. This product is widely available as an over-the-counter (OTC) preparation, reflecting its established profile for general use. It is a single active ingredient product, typically provided in the tablet or capsule drug formulations for oral administration. The drug is designed to mitigate symptoms through its dual action: reducing the labyrinthine excitability of the inner ear's balance system and suppressing the vomiting center located in the brain's medulla. This mechanism provides stabilization against motion-induced symptoms, which is its defined therapeutic benefit.

Regulatory References

  1. NIH LiverTox: Cyclizine
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What side effects are possible with Reisziekte?

Possible Side Effects and Safety Information

The safety profile of this medicine is characterized by adverse reactions that are classified by regulatory authorities based on observed frequency in clinical use and post-marketing surveillance. These effects are officially grouped by the System-Organ Class (SOC) they affect, reflecting the drug’s properties as a first-generation H₁-receptor antagonist.

Frequency-Classified Adverse Reactions

The most frequently documented effects, classified as Common (affecting up to 1 in 10 users), involve the Nervous System and anticholinergic action. These include drowsiness, fatigue, dry mouth, headache, and blurred vision.

Less frequent effects, classified as Uncommon or Rare, involve other systems. Uncommon effects may include constipation, urinary retention, and paradoxical stimulation such as insomnia or nervousness. Effects on the cardiovascular system, such as tachycardia or hypotension, are also documented.

Serious Adverse Reactions and Safety Constraints

Specific events are documented in regulatory labeling as Rare or clinically significant. These Serious Adverse Reactions include hepatic dysfunction, cholestatic jaundice, convulsions, blood dyscrasias (like hemolytic anemia), and hypersensitivity reactions (including angioedema).

Safety notes specify that drowsiness may be particularly prominent at the start of treatment. Furthermore, specific safety considerations apply to certain groups: Older adults may be at an increased risk for side effects, particularly sedation, dizziness, and hypotension. The medication is officially contraindicated in individuals with severe hepatic impairment and requires caution in patients with conditions sensitive to anticholinergic effects, such as narrow-angle glaucoma or prostatic hypertrophy.

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Overdose and Emergency Response

Overdose and When to Seek Help

The official regulatory profile for Cyclizine (Reisziekte) overdose focuses on severe manifestations of Central Nervous System (CNS) toxicity and peripheral anticholinergic syndrome. Documented presentations include CNS effects such as disorientation, hallucinations, ataxia, and convulsions, alongside signs like tachycardia, blurred vision, and urinary retention.


Mandatory Emergency Action

In any case of suspected or known overdose, the official regulatory mandate is to contact a doctor or nearest hospital emergency department immediately. This requirement is due to the documented risk of life-threatening outcomes, including respiratory depression and cardiac arrhythmias.


Overdose Management and Risk

Management is constrained to supportive and symptomatic treatment, as no specific antidote is available. Procedural instructions documented in official sources include the use of gastric lavage and administration of parenteral anticonvulsant therapy to manage seizures.

A key population-specific consideration is the increased susceptibility of younger children to severe CNS effects. In this group, doses exceeding 40 mg/kg are officially associated with a high incidence of convulsions, underscoring the need for immediate medical evaluation.

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Therapeutic Uses of Reisziekte

What Reisziekte Treats: Main Uses and Benefits

The medication Reisziekte (Cyclizine) is generally considered relevant across therapeutic domains where acute sickness and balance disturbances may create noticeable physiological strain. It is applied across areas where short-term symptomatic assistance is needed to control distressing manifestations of nausea and vertigo. Its uses are specific and therapeutically focused.

Therapeutic Focus and Key Benefits

The medication's primary therapeutic role is to help with the prevention and symptomatic relief of kinetosis (motion sickness), and is also applied in addressing sickness linked to vestibular disorders (like Ménière's disease), postoperative nausea and vomiting (PONV), and emetic effects from necessary opioid analgesics or radiotherapy. Its function is to help address symptom clusters that may become intense or disruptive, specifically nausea, vomiting, and dizziness. The use of this medication helps support patients during difficult episodes, contributing to easing the overall symptom load during periods of heightened symptoms.


Quick Fact: Therapeutic Support

Quick Fact: Therapeutic support for Symptoms that interfere with daily functioning (Nausea, Vomiting, Dizziness).

Regulatory References

  1. UK Medicines and Healthcare products Regulatory Agency
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Eligibility and Restrictions for Use

The official regulatory profile for Reisziekte (Cyclizine) establishes clear rules for its use based strictly on age, pre-existing conditions, and physiological status.

Absolute Exclusions (Contraindications)

The medicine is strictly contraindicated and must not be used by patients with a known hypersensitivity to cyclizine or its excipients, or in cases of acute alcohol intoxication. Furthermore, use is prohibited for patients with the severe metabolic disorder Porphyria. Specific tablet formulations are also restricted for individuals with certain rare hereditary metabolic issues like galactose intolerance.

Restricted Use and Special Caution

Regulatory documents require the medicine be used with caution in patients who have certain comorbidities where anticholinergic effects are a concern. These include glaucoma, urinary retention, and obstructive disease of the gastrointestinal tract. Caution is also mandatory for patients with hepatic disease, severe heart failure, acute myocardial infarction, hypertension, or epilepsy.

Age and Physiological Status

The medicine is allowed for adults and children aged 6 years and over. It is explicitly not recommended for children under the age of 6 years. Due to the absence of definitive human data and the excretion of the substance in human milk, use during both pregnancy and breastfeeding is officially not advised.

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What should I know about interactions with other medicines?

Interactions with other medicines and products

The interaction profile for Reisziekte (Cyclizine) is based predominantly on pharmacodynamic interactions that result in additive effects when combined with certain substance classes.


Officially Documented Restrictions

The medicine is contraindicated in the presence of acute alcohol intoxication. Regulatory documents state that the anti-emetic properties of Cyclizine may increase the toxicity of alcohol, and co-administration with alcohol must be avoided entirely.

Interactions with Additive Effects

Co-administration with other Central Nervous System (CNS) Depressants may result in additive effects, increasing the potential for sedation. This category includes substances such as hypnotics, tranquillisers, anaesthetics, antipsychotics, and barbiturates.

Cyclizine may also produce an additive antimuscarinic action with other anticholinergic drugs. This interaction may enhance side-effects when the medicine is combined with agents like tricyclic antidepressants and Monoamine Oxidase Inhibitors ( MAOIs).

Furthermore, the medicine enhances the soporific effect of Opioid Analgesics, specifically Pethidine.

Interaction with Ototoxic Drugs

The drug may mask the warning signs of damage caused by ototoxic drugs, such as aminoglycoside antibacterials. This is a critical interaction-context constraint that obscures a sign of toxicity from the co-administered medicine.

Timing Condition

For the prevention of motion sickness, official labeling requires the medication be taken about one to two hours before departure.

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Mechanism of Action

How Reisziekte Works

The compound functions as a competitive antagonist with a high degree of selectivity for muscarinic cholinergic receptors, primarily the M1 and M3 subtypes. This binding interaction occurs within critical components of the central nervous system, specifically the vestibular nuclei and the reticular formation. Antagonism at these sites prevents the binding of the endogenous ligand, acetylcholine.

Inhibition of muscarinic signal transduction reduces the afferent neural excitability originating from the vestibular apparatus. This action modulates the downstream signal cascade involved in integrating sensory inputs related to movement and spatial orientation. Furthermore, the mechanism of action may involve influencing mathrmGABAA receptor-mediated inhibitory neurotransmission. The resulting physiological consequence is the dampening of aberrant signal traffic and the adjustment of excitatory/inhibitory input balance in central processing centers.

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Dosage and Administration Information

Reisziekte (Cyclizine) is administered through the oral route as a 50 mg tablet or via the parenteral route as a 50 mg/mL injection solution, supporting both intramuscular (IM) and intravenous (IV) delivery methods. The administration protocol is structured by age and the form used.

For adults and children over 12 years, the standard single oral dose is 50 mg. This dose may be repeated, but official guidelines restrict the frequency to a maximum of three times daily, mandating a minimum interval of at least 8 hours between doses. The resulting maximum daily adult intake is 150 mg. The tablet form may be taken with or without food. For motion sickness prevention, the initial oral dose is administered one to two hours before the anticipated travel time.

For children aged 6 to 12 years, the standard oral dose is 25 mg. The use of the oral tablet form is officially not recommended for children under 6 years of age.

When administered parenterally, the standard adult IM or IV dose is 50 mg. Specific procedural constraints apply to intravenous use: the solution must be delivered slowly over a period of at least 3 to 5 minutes. It may be diluted with fluids such as Sodium Chloride 0.9% to ensure the required slow rate of administration. Usage duration is typically short-term for acute events, but it may be prescribed for longer courses in specific chronic conditions.

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Recent Clinical Evidence

Clinical Research for Motion Sickness

The medical approach to motion sickness (Reisziekte) focuses on counteracting the sensory mismatch between visual input and inner ear balance signals.

Recent clinical trials and reviews have concentrated on the effectiveness and side effect profiles of established and novel pharmacological and behavioral countermeasures.

Pharmacological Agents

Evidence from systematic reviews indicates that several drug classes are associated with a reduced incidence of motion sickness symptoms, particularly when taken before the onset of motion. The two main classes evaluated in large studies are:

  • Anticholinergics (e.g., Scopolamine): Generally considered the most effective drug class for prevention, often administered via a transdermal patch for sustained effect. Studies show high preventative efficacy against symptoms like nausea and vomiting.
  • First-Generation Antihistamines (e.g., Dimenhydrinate, Meclizine): These agents have also been shown to influence symptom development. A key limitation observed in trials is the common occurrence of side effects, such as drowsiness or sedation, which may impact performance of tasks like driving.

Newer research has explored novel agents, such as neurokinin-1 (NK1) receptor antagonists, which were investigated in randomized, controlled studies for their potential in reducing the incidence of vomiting associated with varied sea conditions.

Non-Pharmacological Strategies

Research confirms that behavioral and environmental adjustments are essential countermeasures. Observed strategies supported by evidence include:

  • Visual Focus: Directing the gaze toward a stable visual horizon or a distant stationary point to synchronize visual input with the vestibular system.
  • Positioning: Selecting a low-motion location within the vehicle, such as over the wing in an airplane or the front seat of a car.
  • Habituation: Repeated, controlled exposure to motion stimuli can result in desensitization over time, an effect that is sometimes compared favorably to drug effectiveness.
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Frequently Asked Questions (FAQ)

Common questions about Reisziekte (FAQ)

Q: What is Reisziekte?

A: Reisziekte is a term used in Dutch meaning travel sickness or motion sickness.

Motion sickness is a common disturbance of the inner ear caused by repeated motion. It occurs when the brain receives conflicting signals about motion and balance from different parts of the body, such as the eyes, inner ears, and sensory nerves.

Q: What are the typical symptoms of motion sickness?

A: Symptoms of motion sickness can vary but commonly include:

  • Nausea (feeling sick to your stomach)
  • Vomiting
  • Dizziness or lightheadedness
  • Feeling unwell or generally uncomfortable
  • Cold sweats
  • Increased salivation

These symptoms can appear quickly when traveling in a car, boat, train, or plane.

Q: What causes motion sickness when traveling?

A: Motion sickness is caused by a mismatch of sensory information perceived by the brain. When you are moving, your inner ear's balance-sensing system (the vestibular system) detects the motion, but your eyes and other parts of your body may send signals to the brain that you are stationary. This confusion leads to the symptoms of motion sickness.

Q: Can motion sickness be treated?

A: Yes, motion sickness can often be prevented or treated with both non-drug and drug options. The specific approach depends on the severity of the symptoms and the type of travel.

  • Non-drug methods include focusing on a stable object outside the vehicle, taking control of the vehicle (if possible), or getting fresh air.
  • Medications for motion sickness, typically antihistamines or anticholinergics, work by blocking the signals in the brain that trigger nausea and vomiting. These are usually taken before travel.

Consulting a healthcare provider is recommended for personalized advice on treatment.

Q: What is the main class of drug used to treat motion sickness?

A: The main class of over-the-counter drugs used to prevent and treat motion sickness is antihistamines. These include medications like dimenhydrinate or diphenhydramine.

These drugs work by affecting the balancing mechanisms in the inner ear and blocking the brain's signals that cause vomiting. For many people, these are effective, but they can cause side effects like drowsiness.

Q: Is there a non-oral option for preventing severe motion sickness?

A: Yes. For individuals experiencing severe motion sickness, a transdermal patch containing the drug scopolamine (also known as hyoscine) may be prescribed. The patch is typically applied behind the ear and releases the medication slowly over a few days.

This method bypasses the digestive system and can be effective for longer trips, such as on a cruise. It is a prescription-only option in many places and can cause side effects like a dry mouth or blurred vision.

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How should Reisziekte be stored and disposed of?

How to Store and Dispose of Reisziekte? (Cyclizine)

Official regulatory labeling defines specific constraints for storing and disposing of this medicine (Cyclizine Hydrochloride).

Required Storage Conditions

The required storage temperature for tablets and capsules is below 30 C (86 F). The product must be stored in its original container to maintain labeled stability.

Child Safety and Handling

Mandatory regulatory requirements state that the medicine must be kept out of the sight and reach of children.

Disposal Requirements

Expired or unused product must be disposed of according to local requirements. The medicine must not be thrown into wastewater or regular household trash. Disposal should occur through an official pharmaceutical take-back scheme or authorized collection point.

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

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