Product image of Maxolon (Metoclopramide Hydrochloride Monohydrate) supplied by GNH India

Maxolon

Active Ingredient:
Metoclopramide Hydrochloride Monohydrate
Origin:
EU

Maxolon (Metoclopramide Hydrochloride Monohydrate)

Metoclopramide, the active ingredient in Maxolon, is an antiemetic and prokinetic presented as an injectable solution for intramuscular and intravenous use. It is employed to treat nausea and vomiting, postoperative nausea and vomiting, migraine‑associated nausea, and gastroparesis in adult patients. The drug acts centrally on the chemoreceptor trigger zone and peripherally to accelerate gastric emptying, providing rapid relief in acute settings.

GNH India supplies Maxolon as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. Our distribution network ensures timely delivery and regulatory compliance across multiple regions.

Manufacturer / TM Owner

Amdipharm Limited

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Indications & Clinical Uses

Metoclopramide is used to manage conditions involving nausea, vomiting and delayed gastric emptying.

  • Nausea and vomiting: reduces frequency and severity of acute and chronic episodes in adult patients.
  • Post‑operative nausea and vomiting: prevents and treats nausea after surgical procedures, improving patient comfort.
  • Migraine‑associated nausea: alleviates nausea accompanying migraine attacks, supporting overall migraine management.
  • Gastroparesis: enhances gastric motility and accelerates emptying, reducing symptoms such as early satiety and bloating.

How It Works

  • Metoclopramide acts as a dopamine D2‑receptor antagonist in the chemoreceptor trigger zone of the medulla, thereby suppressing the vomiting reflex. It also blocks peripheral D2 receptors in the gastrointestinal tract, increasing acetylcholine release, which enhances smooth‑muscle contractility and promotes coordinated gastric emptying. These actions result in rapid control of nausea and improvement of gastric motility in affected patients.

Side Effects

Metoclopramide may cause a range of adverse reactions, which are grouped by frequency and severity.

Common Side Effects

  • Drowsiness: feeling of sleepiness or reduced alertness.
  • Fatigue: general tiredness or lack of energy.
  • Restlessness: uneasy feeling, often described as akathisia.
  • Diarrhea: loose, watery stools.

Serious or Rare Side Effects

  • Extrapyramidal symptoms: involuntary muscle movements, dystonia, or tremor.
  • Tardive dyskinesia: persistent, potentially irreversible facial or tongue movements.
  • Neuroleptic malignant syndrome: life‑threatening reaction with fever, muscle rigidity, and autonomic instability.

Precautions & Warnings

When using Metoclopramide, clinicians should observe several safety considerations to minimize risks.

  • Assess renal and hepatic function: adjust use in patients with impairment.
  • Use the lowest effective dose: limit exposure to reduce side‑effect risk.
  • Monitor for extrapyramidal symptoms: watch for muscle rigidity, tremor or abnormal movements.
  • Avoid in patients with known hypersensitivity: discontinue if allergic reaction occurs.
  • Caution in pregnancy and lactation: category B1, benefits must outweigh potential risks.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Metoclopramide can interact with other medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Antipsychotics (dopamine antagonists): additive risk of extrapyramidal effects.
  • MAO inhibitors: may precipitate hypertensive crisis.
  • CYP2D6 inhibitors (e.g., quinidine): increase metoclopramide plasma concentrations.

Moderate Interactions (Monitor Closely)

  • CNS depressants (sedatives, antihistamines): enhanced drowsiness or sedation.
  • Opioids: may potentiate gastrointestinal motility effects.
  • SSRIs or SNRIs: increased risk of serotonin syndrome.

Frequently Asked Questions

Maxolon contains metoclopramide and is indicated for the treatment of nausea and vomiting, postoperative nausea and vomiting, migraine‑associated nausea, and gastroparesis. It helps control acute episodes of emesis and improves gastric emptying in patients with delayed stomach motility.

Metoclopramide blocks dopamine D2 receptors in the chemoreceptor trigger zone, suppressing the vomiting reflex, and also antagonises peripheral D2 receptors in the gut, increasing acetylcholine release. This dual action enhances gastrointestinal motility and provides anti‑emetic effects.

The dose of Maxolon is determined by the prescribing clinician based on the patient’s condition, severity of symptoms, and route of administration. Dosage may vary for adults, elderly patients, and those with renal or hepatic impairment, and should follow local prescribing guidelines.

Metoclopramide is classified as pregnancy category B1, indicating no evidence of risk in animal studies but limited human data. It may be used during pregnancy only if the potential benefit justifies the risk. Metoclopramide passes into breast milk in small amounts; breastfeeding decisions should be made with a healthcare professional.

To order Maxolon, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain where required) and necessary import documentation.

Compared with other dopamine antagonists such as domperidone, metoclopramide has central anti‑emetic activity in addition to peripheral pro‑kinetic effects. It is often preferred when rapid control of nausea is needed, but it carries a higher risk of extrapyramidal side effects, requiring careful monitoring.

Maxolon should be stored at 2‑8 °C, kept refrigerated, protected from light, and must not be frozen or shaken. Maintain the cold‑chain during transport and store in the original packaging until ready for use.

Maxolon is supplied as an injectable solution for intramuscular or intravenous administration. The route, rate of infusion, and duration are determined by the prescriber, taking into account the clinical situation and patient characteristics.

Serious adverse reactions include extrapyramidal symptoms such as dystonia, tardive dyskinesia, and neuroleptic malignant syndrome. These events are rare but can be life‑threatening and require immediate medical attention. Monitoring for early signs is essential, especially with prolonged therapy.

Maxolon is contraindicated in patients with known hypersensitivity to metoclopramide or any component of the formulation, and in those with pheochromocytoma or gastrointestinal obstruction. Caution is advised in patients with Parkinson’s disease, seizure disorders, or severe depression.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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