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Metomide injection is a parenteral form of metoclopramide, a dopamine (D₂) receptor antagonist with prokinetic and antiemetic properties. It is used to manage nausea, vomiting, and delayed gastric emptying (gastroparesis). The injectable form is typically used in hospital or clinical settings.
Active ingredient: Metoclopramide (10 mg per ampoule)
Inactive / excipients: (formulation-specific) possibly water for injection, buffering agents, stabilizers — check manufacturer’s insert
Antiemetic / Prokinetic / Dopamine D₂ antagonist
Sterile injectable solution (ampoule) — 10 mg per ampoule (volume as per manufacturer)
Metomide injection may be used in:
Prevention or treatment of nausea and vomiting, including postoperative, chemotherapy-induced, or drug-induced vomiting
Management of gastroparesis or delayed gastric emptying (e.g. in diabetic patients)
As a prokinetic agent to stimulate GI motility in certain diagnostic procedures (e.g. to facilitate gastric emptying)
The exact dose and frequency depend on patient condition, route (IV or IM), and physician’s orders.
In many protocols, 10 mg (one ampoule) may be given IV or IM, repeated as needed.
For gastroparesis, such injections are often given up to 4 times daily in clinical practice.
Symptoms: sedation, lethargy, extrapyramidal symptoms (dystonia, muscle spasms), hypotension, agitation, restlessness
Treatment: supportive care, discontinue drug, manage extrapyramidal reactions (use anticholinergics or antihistamines), monitor vital signs
In clinical settings with injections, “missed dose” is usually handled by medical staff.
Patients shouldn’t self-administer extra dose to compensate.
Administer by intravenous (IV) or intramuscular (IM) route using aseptic technique.
For IV use, the injection should be given slowly to reduce side effect risks.
Monitor patient for response and adverse effects during and after administration.
Metoclopramide (Metomide) should not be used in:
Known hypersensitivity to metoclopramide or formulation ingredients
Gastrointestinal hemorrhage, obstruction, or perforation
Pheochromocytoma (risk of hypertensive crisis)
Parkinson’s disease or other extrapyramidal disorders
Use beyond 12 weeks due to risk of tardive dyskinesia (movement disorder)
Common / less serious:
Drowsiness, fatigue
Diarrhea
Restlessness, agitation
Extrapyramidal reactions: acute dystonia, akathisia
Serious / rare:
Tardive dyskinesia (potentially irreversible) if used long-term
Neuroleptic malignant syndrome (rare)
Galactorrhea, gynecomastia (due to hyperprolactinemia)
Others: movement disorders, extrapyramidal symptoms even after short term use
Limit use to short duration (≤ 12 weeks) to reduce risk of movement disorders
Use with caution in elderly who are more sensitive to side effects
Monitor for extrapyramidal symptoms; discontinue if they appear
In renal impairment, dose adjustment may be needed
Avoid in patients with GI obstruction, bleeding, or perforation
Avoid combining with other drugs that increase risk of movement disorders
Additive risk of extrapyramidal effects with other dopamine antagonists or antipsychotics
May interact with medications impacting CYP2D6 or dopamine pathways
Drugs with sedative properties (e.g. antihistamines, benzodiazepines) may worsen drowsiness
Store at controlled room temperature (per manufacturer guidelines)
Keep away from light and moisture
Do not freeze
Use before expiry date
Dispose of unused/expired ampoules safely per biomedical waste protocols
Metoclopramide is not a narcotic or controlled drug, but it is prescription-only and must be used under physician supervision
Monitor patients closely for movement disorders, particularly in prolonged therapy
Administer IV slowly to minimize side effects
Use the lowest effective dose for shortest duration
Discontinue if signs of TD (tardive dyskinesia) or extrapyramidal symptoms appear
Caution in elderly and in patients with renal impairment
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