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Reglan

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Used to prevent nausea and vomiting, often following surgery or radiotherapy.


Ingredient
Availability
In Stock
Delivery
Airmail (14-21 days) | EMS trackable (5-9 days)
Product is shipped in a fully discreet envelope with no content disclosure, including all required documentation inside

Product Sheet

Alternative/Local Brand
Maxolon
Active Ingredient(s)
Metoclopramide
Primary Category
Nausea and Vomiting Relief
Therapeutic Class
Gastrointestinal system, Antiemetics and antinauseants, Propulsives
Pharmacological Class
Dopamine D2 antagonists
Indications
Nausea, Vomiting, Gastroparesis, Prevention of radiotherapy-induced vomiting
Contraindications
Gastrointestinal obstruction, Epilepsy, Parkinson's disease, Phaeochromocytoma
Minor Side Effects
Restlessness
Moderate Side Effects
Drowsiness, Fatigue, Diarrhoea, Depression
Serious Side Effects
Muscle spasms (extrapyramidal symptoms), Tardive dyskinesia, Neuroleptic malignant syndrome, Cardiac arrest
Dosage Forms
Tablet, Oral solution
Administration Route
Oral
Mechanism of Action
Metoclopramide works by blocking dopamine receptors in the brain's vomiting centre and increasing the movements of the stomach and intestines, helping food pass more quickly.
Prescription Status
Rx
Manufacturer
TEVA UK Ltd
Patient Summary
Used to prevent nausea and vomiting, often following surgery or radiotherapy.
Onset Time
30-60 minutes
Duration
6 hours
Storage Instructions
Keep in the original container away from light.
Drug Interactions
Levodopa, Digoxin, Ciclosporin, Opioid analgesics
Age Restrictions
Restricted use in patients under 18 years; max 5 days treatment.
Pregnancy Use
Can be used during pregnancy if necessary.
Alternative Drugs
Domperidone, Prochlorperazine, Cyclizine

RegLan: Metoclopramide Overview

RegLan is a brand-name medication that contains the active ingredient metoclopramide. Metoclopramide belongs to the class of prokinetic agents used to treat various digestive-health conditions. In Hong Kong, RegLan is available only with a prescription and is supplied as a 10 mg tablet.

How Metoclopramide Works in the Body

Metoclopramide exerts its therapeutic effect through two primary mechanisms:

  • Dopamine D₂-receptor antagonism in the chemoreceptor trigger zone of the brain reduces the sensation of nausea and vomiting.
  • Enhancement of gastrointestinal motility by increasing the responsiveness of the upper gastrointestinal tract to acetylcholine, which promotes coordinated muscle contractions that move food through the stomach and intestines more efficiently.

These actions result in a faster gastric emptying rate and less reflux of stomach contents into the esophagus. Oral tablets are rapidly absorbed, reaching peak plasma concentrations within 1-2 hours. The drug is largely metabolized in the liver and eliminated in the urine, with a plasma half-life of roughly 5-6 hours.

Conditions Treated with RegLan

RegLan (metoclopramide) is approved in Hong Kong for the following indications:

  • Nausea and vomiting associated with postoperative recovery, chemotherapy, and migraine.
  • Gastro-esophageal reflux disease (GERD) when symptoms are not adequately controlled by standard acid-suppression therapy.
  • Gastroparesis (delayed stomach emptying) in adults, particularly when caused by diabetic neuropathy or idiopathic dysfunction.

These uses reflect the drug’s dual anti-emetic and prokinetic properties. The typical patient is an adult who requires symptomatic relief from nausea or needs improved gastric motility to facilitate digestion.

Evidence-Based Off-Label Uses

  • Lactation promotion - Some clinical studies have shown that metoclopramide can increase prolactin levels and thereby enhance breast-milk production. This use is not approved by the Hong Kong Department of Health and should only be considered under close medical supervision because of the risk of neurologic side effects.

Disclaimer: Off-label use requires individualized risk assessment and close monitoring by a qualified healthcare professional.

Who Should Use RegLan? Contra-indications and Precautions

Absolute Contra-indications

  • Known hypersensitivity to metoclopramide or any excipients in the tablet.
  • Pseudoparkinsonism or any condition that predisposes to extrapyramidal movement disorders.
  • Severe hepatic impairment (the drug’s metabolism is significantly reduced).
  • Use in pregnancy beyond the first trimester is contraindicated due to evidence of fetal harm.

Relative Contra-indications

  • Renal insufficiency - dose adjustment may be needed.
  • Elderly patients - increased sensitivity to central nervous system effects; monitor closely for confusion or dizziness.
  • History of seizure disorders - metoclopramide can lower the seizure threshold.

Special Populations

  • Breastfeeding - short-term use may be permissible, but long-term exposure is discouraged.
  • Pediatric use - not recommended for children under 18 years for most indications because of heightened risk of extrapyramidal reactions.

Safety Profile: Side Effects and Interactions

Common Side Effects

  • Drowsiness or fatigue (often described as “tiredness”).
  • Restlessness or mild agitation.
  • Diarrhea or abdominal cramping due to increased gut motility.

These effects are usually transient and lessen as the body adjusts to the medication.

Serious Adverse Events

  • Extrapyramidal symptoms (e.g., acute dystonia, akathisia) that may appear within the first few days of therapy. Immediate medical evaluation is required.
  • Tardive dyskinesia, a potentially irreversible movement disorder, especially after prolonged treatment (>12 weeks).
  • Neuroleptic malignant syndrome - rare but life-threatening; characterized by high fever, muscle rigidity, and altered mental status.

If any of these serious reactions occur, discontinue RegLan and seek urgent care.

Drug Interactions

  • CYP2D6 substrates (e.g., codeine, tramadol) - metoclopramide can inhibit metabolism, increasing plasma levels of these agents.
  • Anticholinergic drugs (e.g., atropine, scopolamine) - may reduce the prokinetic effect of metoclopramide.
  • Other dopamine antagonists (e.g., antipsychotics) - additive risk of extrapyramidal side effects.

Patients should inform their prescriber about all current medications, over-the-counter products, and herbal supplements.

Food and Lifestyle Interactions

  • Metoclopramide can be taken with or without food; however, taking it with a small amount of food may lessen gastrointestinal upset.
  • Alcohol does not have a known pharmacokinetic interaction, but excessive consumption can exacerbate drowsiness.
  • Caution when driving or operating machinery until the individual knows how the medication affects them.

How to Take RegLan

  • Standard dosing - The usual adult regimen starts with 10 mg taken orally 30 minutes before meals and at bedtime, up to four times per day. The total daily dose should not exceed 40 mg.
  • Renal or hepatic impairment - Dose may need to be reduced; a physician will determine the appropriate adjustment.
  • Tablet administration - Swallow the tablet whole with a glass of water; do not crush or chew, as this can affect drug absorption.
  • Missed dose - If a dose is missed, take it as soon as remembered unless the next scheduled dose is within a few hours. Do not double the dose.
  • Overdose - Symptoms may include severe drowsiness, agitation, or seizures. Seek emergency medical attention; supportive care is the mainstay of treatment.
  • Discontinuation - If therapy is to be stopped after prolonged use, gradual tapering over several days is advisable to lower the risk of withdrawal dyskinesia.

Monitoring and Follow-Up

  • Neurologic assessment - Patients on metoclopramide for more than 12 weeks should have periodic evaluations for early signs of tardive dyskinesia.
  • Renal and hepatic function - Baseline labs are recommended before initiating therapy; repeat testing may be needed for patients with known organ dysfunction.
  • Blood glucose - In diabetic patients, improved gastric emptying can affect glucose control; monitor blood sugar levels accordingly.

Regular follow-up appointments enable clinicians to adjust dosing, assess efficacy, and identify adverse effects early.

Storage and Handling

  • Keep tablets at room temperature (15 °C - 30 °C).
  • Protect from moisture and direct sunlight.
  • Keep the container tightly closed and out of reach of children.
  • Do not use the medication after the expiration date printed on the package.
  • Dispose of unused tablets according to local pharmacy-take-back programs or the instructions on the label.

Medication-Specific Glossary

Extrapyramidal symptoms
Unwanted movements such as muscle rigidity, tremor, or involuntary muscle contractions caused by dopamine antagonism in the central nervous system.
Tardive dyskinesia
A potentially irreversible disorder characterized by repetitive, involuntary movements, often of the face and tongue, that can arise after long-term use of dopamine-blocking agents.
Prokinetic
A drug that enhances gastrointestinal motility, facilitating the movement of contents through the digestive tract.
D₂-receptor antagonist
A substance that blocks dopamine D₂ receptors, reducing nausea signals from the brain’s chemoreceptor trigger zone.

Medical Disclaimer

This article provides educational information about RegLan and is not a substitute for professional medical advice. Treatment decisions, including use for unapproved indications, must be made under the guidance of a qualified healthcare provider. The content is intended for informational purposes and does not constitute medical recommendations. Always consult a physician before starting, stopping, or changing any medication regimen.

Reglan FAQ

Can RegLan be used for short-term nausea relief after surgery?

Yes. Metoclopramide’s anti-emetic action makes it suitable for postoperative nausea when prescribed for a limited duration, typically a few days, under physician supervision.

What are the visible differences between RegLan tablets and generic metoclopramide?

RegLan tablets are usually round, white, and bear the imprint “10 MG” with the brand logo. Generic versions may vary in size, shape, or imprint but contain the same 10 mg dose of metoclopramide.

Is metoclopramide safe for pregnant women in Hong Kong?

Metoclopramide is contraindicated after the first trimester because animal studies and limited human data suggest potential risks to the developing fetus. Pregnant patients should discuss alternative treatments with their obstetrician.

How long should a patient stay on RegLan before tapering is required?

If therapy extends beyond 12 weeks, clinicians generally recommend a gradual taper over several days to reduce the risk of withdrawal dyskinesia. Shorter courses typically do not require tapering.

Can RegLan interact with antidepressants such as SSRIs?

Metoclopramide may increase serotonin levels when combined with SSRIs, potentially raising the risk of serotonin syndrome. Patients should alert their prescriber if they are taking any antidepressant medication.

What should a traveler know about taking RegLan on an international flight?

RegLan tablets are permitted in both carry-on and checked luggage for personal medical use. Carry the prescription label and a copy of the doctor's note in case customs officials request documentation.

Are there any dietary restrictions while taking RegLan?

There are no strict food prohibitions, but taking the tablet with a light meal can lessen stomach irritation. Avoid excessive alcohol, which may amplify drowsiness.

How does RegLan differ from other anti-emetics like ondansetron?

Metoclopramide works by blocking dopamine receptors, whereas ondansetron antagonizes serotonin 5-HT₃ receptors. Metoclopramide also promotes gastric motility, a property ondansetron lacks.

What is the typical cost difference between RegLan and generic metoclopramide in Hong Kong?

Brand-name RegLan is generally priced higher than locally manufactured generic tablets due to brand premiums and marketing costs. Exact pricing varies by pharmacy and insurance coverage.

Can RegLan be used by pilots or other safety-critical workers?

Because metoclopramide can cause drowsiness or extrapyramidal symptoms, safety-critical professionals should assess their fitness to work after starting the medication and may need to undergo a medical evaluation before resuming duties.

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