Metoclopramide (oral)

Metoclopramide (oral)
Black Box Warning
Adult Indications & Dosage
Pediatric Indications & Dosage
Contraindications
Warnings & Precautions
Adverse Reactions
Drug Interactions
Use in Specific Populations
Administration & Monitoring
Overdosage
Pharmacology
Clinical Studies
How Supplied
Images
Patient Counseling Information
Precautions with Alcohol
Brand Names
Look-Alike Names

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Kiran Singh, M.D. [2]

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Black Box Warning

WARNING: TARDIVE DYSKINESIA See full prescribing information for complete Boxed Warning. * Treatment with metoclopramide can cause tardive dyskinesia, a serious movement disorder that is often irreversible. The risk of developing tardive dyskinesia increases with the duration of treatment and the total cumulative dose. Metoclopramide therapy should be discontinued in patients who develop signs or symptoms of tardive dyskinesia. There is no known treatment for tardive dyskinesia. In some patients, symptoms may lessen or resolve after metoclopramide treatment is stopped. Treatment with metoclopramide for longer than 12 weeks should be avoided in all but rare cases where therapeutic benefit is thought to outweigh the risk of developing tardive dyskinesia.

Overview

Metoclopramide (oral) is a {{{drugClass}}} that is FDA approved for the treatment of symptoms due to gastroesophageal reflux and diabetic gastroparesis. There is a Black Box Warning for this drug as shown here. Common adverse reactions include headache, nausea, vomiting, fatigue, and somnolence.

Adult Indications and Dosage

FDA-Labeled Indications and Dosage (Adult)

Condition1

• Dosing Information

• Dosage

Condition2

• Dosing Information

• Dosage

Condition3

• Dosing Information

• Dosage

Condition4

• Dosing Information

• Dosage

Off-Label Use and Dosage (Adult)

Guideline-Supported Use

Condition1

• Developed by:

• Class of Recommendation:

• Strength of Evidence:

• Dosing Information

• Dosage

Condition2

There is limited information regarding Off-Label Guideline-Supported Use of Metoclopramide (oral) in adult patients.

Non–Guideline-Supported Use

Condition1

• Dosing Information

• Dosage

Condition2

There is limited information regarding Off-Label Non–Guideline-Supported Use of Metoclopramide (oral) in adult patients.

Pediatric Indications and Dosage

FDA-Labeled Indications and Dosage (Pediatric)

Condition1

• Dosing Information

• Dosage

Condition2

There is limited information regarding FDA-Labeled Use of Metoclopramide (oral) in pediatric patients.

Off-Label Use and Dosage (Pediatric)

Guideline-Supported Use

Condition1

• Developed by:

• Class of Recommendation:

• Strength of Evidence:

• Dosing Information

• Dosage

Condition2

There is limited information regarding Off-Label Guideline-Supported Use of Metoclopramide (oral) in pediatric patients.

Non–Guideline-Supported Use

Condition1

• Dosing Information

• Dosage

Condition2

There is limited information regarding Off-Label Non–Guideline-Supported Use of Metoclopramide (oral) in pediatric patients.

Contraindications

• Condition1

Warnings

WARNING: TARDIVE DYSKINESIA See full prescribing information for complete Boxed Warning. * Treatment with metoclopramide can cause tardive dyskinesia, a serious movement disorder that is often irreversible. The risk of developing tardive dyskinesia increases with the duration of treatment and the total cumulative dose. Metoclopramide therapy should be discontinued in patients who develop signs or symptoms of tardive dyskinesia. There is no known treatment for tardive dyskinesia. In some patients, symptoms may lessen or resolve after metoclopramide treatment is stopped. Treatment with metoclopramide for longer than 12 weeks should be avoided in all but rare cases where therapeutic benefit is thought to outweigh the risk of developing tardive dyskinesia.

• Description

Precautions

• Description

Adverse Reactions

Clinical Trials Experience

There is limited information regarding Clinical Trial Experience of Metoclopramide (oral) in the drug label.

Body as a Whole

Cardiovascular

Digestive

Endocrine

Hematologic and Lymphatic

Metabolic and Nutritional

Musculoskeletal

Neurologic

Respiratory

Skin and Hypersensitivy Reactions

Special Senses

Urogenital

Miscellaneous

Postmarketing Experience

There is limited information regarding Postmarketing Experience of Metoclopramide (oral) in the drug label.

Body as a Whole

Cardiovascular

Digestive

Endocrine

Hematologic and Lymphatic

Metabolic and Nutritional

Musculoskeletal

Neurologic

Respiratory

Skin and Hypersensitivy Reactions

Special Senses

Urogenital

Miscellaneous

Drug Interactions

• Drug

• Description

Use in Specific Populations

Pregnancy

Pregnancy Category (FDA):

• Pregnancy Category

Pregnancy Category (AUS):

• Australian Drug Evaluation Committee (ADEC) Pregnancy Category

There is no Australian Drug Evaluation Committee (ADEC) guidance on usage of Metoclopramide (oral) in women who are pregnant.

Labor and Delivery

There is no FDA guidance on use of Metoclopramide (oral) during labor and delivery.

Nursing Mothers

There is no FDA guidance on the use of Metoclopramide (oral) with respect to nursing mothers.

Pediatric Use

There is no FDA guidance on the use of Metoclopramide (oral) with respect to pediatric patients.

Geriatic Use

There is no FDA guidance on the use of Metoclopramide (oral) with respect to geriatric patients.

Gender

There is no FDA guidance on the use of Metoclopramide (oral) with respect to specific gender populations.

Race

There is no FDA guidance on the use of Metoclopramide (oral) with respect to specific racial populations.

Renal Impairment

There is no FDA guidance on the use of Metoclopramide (oral) in patients with renal impairment.

Hepatic Impairment

There is no FDA guidance on the use of Metoclopramide (oral) in patients with hepatic impairment.

Females of Reproductive Potential and Males

There is no FDA guidance on the use of Metoclopramide (oral) in women of reproductive potentials and males.

Immunocompromised Patients

There is no FDA guidance one the use of Metoclopramide (oral) in patients who are immunocompromised.

Administration and Monitoring

Administration

• Oral

• Intravenous

Monitoring

There is limited information regarding Monitoring of Metoclopramide (oral) in the drug label.

• Description

IV Compatibility

There is limited information regarding IV Compatibility of Metoclopramide (oral) in the drug label.

Overdosage

Acute Overdose

Signs and Symptoms

• Description

Management

• Description

Chronic Overdose

There is limited information regarding Chronic Overdose of Metoclopramide (oral) in the drug label.

Pharmacology

There is limited information regarding Metoclopramide (oral) Pharmacology in the drug label.

Mechanism of Action

Structure

File:Metoclopramide (oral)01.png

This image is provided by the National Library of Medicine.

Pharmacodynamics

There is limited information regarding Pharmacodynamics of Metoclopramide (oral) in the drug label.

Pharmacokinetics

There is limited information regarding Pharmacokinetics of Metoclopramide (oral) in the drug label.

Nonclinical Toxicology

There is limited information regarding Nonclinical Toxicology of Metoclopramide (oral) in the drug label.

Clinical Studies

There is limited information regarding Clinical Studies of Metoclopramide (oral) in the drug label.

How Supplied

Storage

There is limited information regarding Metoclopramide (oral) Storage in the drug label.

Images

Drug Images

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Package and Label Display Panel

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Patient Counseling Information

There is limited information regarding Patient Counseling Information of Metoclopramide (oral) in the drug label.

Precautions with Alcohol

• Alcohol-Metoclopramide (oral) interaction has not been established. Talk to your doctor about the effects of taking alcohol with this medication.

Brand Names

• METOCLOPRAMIDE HYDROCHLORIDE®

Look-Alike Drug Names

• A® — B®

Drug Shortage Status

Price

References

The contents of this FDA label are provided by the National Library of Medicine.

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