Drug Guide
Metoclopramide Hydrochloride
Classification
Therapeutic: Antiemetic, Gastroprokinetic agent
Pharmacological: Dopamine D2 receptor antagonist
FDA Approved Indications
- Gastroesophageal reflux disease (GERD) with delayed gastric emptying
- Postoperative nausea and vomiting
- Chemotherapy-induced nausea and vomiting
Mechanism of Action
Metoclopramide enhances gastrointestinal motility by blocking dopamine D2 receptors in the chemoreceptor trigger zone and gut, thereby acting as an antiemetic and prokinetic agent.
Dosage and Administration
Adult: Typically 10 mg orally 30 minutes before meals and at bedtime; intravenous doses vary based on indication.
Pediatric: Dosing is weight-based; typically 0.1-0.2 mg/kg/dose 3-4 times daily, not to exceed adult doses.
Geriatric: Start at lower doses due to increased sensitivity and risk of side effects.
Renal Impairment: Dose adjustment may be necessary; consult guidelines.
Hepatic Impairment: Use with caution; monitor closely.
Pharmacokinetics
Absorption: Well absorbed orally, with variable bioavailability.
Distribution: Widely distributed, crosses the blood-brain barrier and placenta.
Metabolism: Metabolized in the liver, partly by conjugation.
Excretion: Excreted mainly in urine.
Half Life: Approximately 5-6 hours.
Contraindications
- Gastrointestinal hemorrhage
- Mechanical bowel obstruction
- Perforation
- History of tardive dyskinesia
Precautions
- Use with caution in Parkinson's disease, depression, and history of neuropsychiatric disorders.
- Pregnancy category B; caution during lactation.
Adverse Reactions - Common
- Fatigue (Frequent)
- Drowsiness (Frequent)
- Restlessness, somnolence (Common)
Adverse Reactions - Serious
- Tardive dyskinesia (Uncommon but serious with long-term use)
- Extrapyramidal symptoms (Uncommon)
- Neuroleptic malignant syndrome (Rare)
Drug-Drug Interactions
- CNS depressants (enhanced sedation)
- Drugs lowering seizure threshold
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor for extrapyramidal symptoms, tardive dyskinesia, and neuropsychiatric effects.
Diagnoses:
- Risk for neurological adverse effects
- Impaired GI motility
Implementation: Administer as prescribed; monitor for side effects; assess symptom relief.
Evaluation: Effectiveness in controlling nausea/vomiting and improving gastric emptying.
Patient/Family Teaching
- Do not exceed prescribed dose.
- Report any involuntary movements or abnormal muscle movements.
- Caution when operating machinery or driving.
- Avoid alcohol and CNS depressants.
Special Considerations
Black Box Warnings:
- Tardive dyskinesia, which can be irreversible, especially with long-term or high-dose use.
Genetic Factors: N/A
Lab Test Interference: N/A
Overdose Management
Signs/Symptoms: Drowsiness, sedation, disorientation, extrapyramidal symptoms.
Treatment: Supportive care; administer activated charcoal if ingestion was recent; monitor and manage symptoms; use of diphenhydramine or benzodiazepines for extrapyramidal reactions, as indicated.
Storage and Handling
Storage: Store at room temperature away from light and moisture.
Stability: Stable when stored properly; consult product label for expiration.