Metoclopramide Hydrochloride 4 mg/mL Oral Suspension is a liquid dosage form in which metoclopramide hydrochloride is uniformly dispersed throughout a liquid medium, ensuring a homogeneous mixture for precise administration. This formulation is primarily used to treat conditions such as gastroesophageal reflux disease (GERD), diabetic gastroparesis, and nausea and vomiting associated with chemotherapy or surgery.

Licensed to fill prescriptions for patients in RI, MA, CT, NJ, NH, FL, ME and PA. New York patients are served on a limited basis while nonresident registration is pending.
Metoclopramide Hydrochloride 4 mg/mL Oral Suspension is a compounded medication designed to effectively manage certain gastrointestinal disorders. This liquid dosage form ensures that one or more ingredients are uniformly dispersed throughout a liquid medium, providing a homogeneous mixture for administration. This formulation is particularly beneficial for patients who have difficulty swallowing tablets or require precise dosing adjustments not available in commercially prepared medications.
This medication works by enhancing gastrointestinal motility without increasing gastric secretions. It is commonly used to treat conditions such as diabetic gastroparesis, where it helps facilitate stomach emptying and alleviates symptoms like nausea, vomiting, and feelings of fullness after meals. By promoting the movement of food through the stomach and intestines, it helps improve nutritional intake and overall digestive comfort.
It reduces reflux by increasing the muscle contractions in the upper digestive tract, which prevents the backflow of stomach contents into the esophagus. Additionally, it is utilized to prevent or relieve nausea and vomiting associated with chemotherapy, radiation therapy, or surgery, enhancing patient comfort during treatment.
For prescribers, this compounded oral suspension allows for customized dosing to meet individual patient needs, especially in pediatric or geriatric populations where standard dosages may not be appropriate. The 4 mg/mL concentration provides flexibility in adjusting doses based on patient response and tolerability, ensuring optimal therapeutic outcomes.
Patients are advised to take this medication exactly as prescribed by their healthcare provider. It should be measured carefully using a proper dosing syringe or cup to ensure accurate dosing. Common side effects may include drowsiness, fatigue, or restlessness. It is important to report any severe or persistent adverse effects, such as uncontrolled muscle movements or changes in mood, to your doctor promptly.
If you have any questions, reach out to us.
Metoclopramide Hydrochloride 4 mg/mL Oral Suspension is a liquid dosage form designed to provide a homogeneous mixture for administration, ensuring consistent dosing and absorption. This formulation is primarily used to treat conditions such as gastroesophageal reflux disease (GERD), diabetic gastroparesis, and to prevent nausea and vomiting associated with chemotherapy or surgery. While effective, it is crucial to be aware of potential drug interactions that may affect the safety and efficacy of metoclopramide.
Metoclopramide is a dopamine receptor antagonist, and its interaction profile is influenced by its mechanism of action. One significant interaction is with other central nervous system (CNS) depressants, such as alcohol, benzodiazepines, opioids, and certain antihistamines. Concurrent use can enhance the sedative effects, leading to increased drowsiness, dizziness, and impaired cognitive function. Patients should be advised to avoid or limit the use of alcohol and consult their healthcare provider before using other CNS depressants.
Another important interaction is with medications that affect the cytochrome P450 enzyme system, particularly CYP2D6 inhibitors. Drugs such as fluoxetine, paroxetine, and quinidine can increase the plasma concentration of metoclopramide, potentially leading to an increased risk of adverse effects like extrapyramidal symptoms and tardive dyskinesia. Prescribers should consider dose adjustments or alternative therapies when these medications are used concomitantly.
Metoclopramide can also interact with monoamine oxidase inhibitors (MAOIs), such as phenelzine and tranylcypromine, leading to an increased risk of hypertensive crisis. It is generally recommended to avoid the use of metoclopramide with MAOIs. Additionally, the use of metoclopramide with selective serotonin reuptake inhibitors (SSRIs) may increase the risk of serotonin syndrome, a potentially life-threatening condition. Symptoms include confusion, agitation, rapid heart rate, and increased body temperature. Patients should be monitored closely for signs of serotonin syndrome, especially when starting or increasing the dose of either medication.
Metoclopramide may also affect the absorption of other medications by altering gastrointestinal motility. For instance, it can decrease the absorption of digoxin and increase the absorption of cyclosporine. Monitoring therapeutic drug levels and adjusting doses as necessary can help mitigate these interactions. Additionally, metoclopramide can enhance the effects of antihypertensive drugs, potentially leading to hypotension. Patients should be monitored for signs of low blood pressure, and dose adjustments may be necessary.
Patients and prescribers should be aware of these potential interactions and take appropriate precautions. It is essential to review all medications, including over-the-counter drugs and supplements, with a healthcare provider to ensure safe and appropriate use of metoclopramide hydrochloride oral suspension. If you have any questions or concerns about drug interactions or the use of this formulation, please reach out to us at Bayview Pharmacy for further assistance.
Metoclopramide Hydrochloride 4 mg/mL Oral Suspension is a liquid dosage form designed to provide a uniform and homogeneous mixture of the active ingredient, metoclopramide hydrochloride, dispersed throughout a liquid medium. This formulation is particularly beneficial for patients who may have difficulty swallowing tablets or require precise dosing adjustments, such as pediatric or geriatric patients. The liquid suspension allows for flexible dosing and ease of administration, ensuring that patients receive the exact amount of medication prescribed by their healthcare provider.
Metoclopramide hydrochloride is a medication that primarily works by enhancing gastrointestinal motility. It acts as a dopamine receptor antagonist, specifically targeting the D2 receptors in the chemoreceptor trigger zone of the central nervous system. By blocking these receptors, metoclopramide helps to prevent nausea and vomiting, which can be particularly useful in conditions such as gastroparesis, where delayed gastric emptying leads to symptoms like nausea, vomiting, and abdominal discomfort. Additionally, metoclopramide increases the tone and amplitude of gastric contractions, facilitating the movement of stomach contents into the small intestine, thereby improving gastric emptying.
In the context of treating gastroesophageal reflux disease (GERD), metoclopramide's prokinetic properties help to enhance the lower esophageal sphincter's tone, reducing the likelihood of acid reflux. This action not only alleviates symptoms such as heartburn and regurgitation but also aids in the healing of esophageal irritation caused by stomach acid. Furthermore, metoclopramide's ability to accelerate gastric emptying can be beneficial in managing symptoms of diabetic gastroparesis, a condition characterized by delayed gastric emptying due to autonomic neuropathy in diabetic patients.
For prescribers, the 4 mg/mL oral suspension offers a versatile option for titrating doses according to the specific needs of the patient. This flexibility is crucial in managing conditions that require varying dosages based on the severity of symptoms or patient response. The liquid form also ensures rapid absorption and onset of action, which is essential in acute settings where prompt relief from symptoms is desired.
Patients using Metoclopramide Hydrochloride 4 mg/mL Oral Suspension should be aware of potential side effects, including drowsiness, fatigue, and, in some cases, extrapyramidal symptoms such as restlessness or involuntary movements. It is important to follow the prescribed dosage and consult with a healthcare provider if any adverse effects are experienced. As with any medication, adherence to the prescribed regimen and open communication with healthcare providers are key to achieving optimal therapeutic outcomes.
If you have any questions or need further information about Metoclopramide Hydrochloride 4 mg/mL Oral Suspension, please reach out to us at Bayview Pharmacy. Our team of compounding pharmacists is here to assist you with any inquiries or concerns you may have regarding this formulation.
Metoclopramide Hydrochloride 4 mg/mL Oral Suspension is a liquid dosage form where the active ingredient, Metoclopramide Hydrochloride, is uniformly dispersed in a liquid medium to create a homogeneous mixture for easy administration.
This medication is primarily used to treat nausea and vomiting, facilitate gastric emptying in patients with delayed stomach emptying, and manage gastroesophageal reflux disease (GERD).
It should be taken as directed by your healthcare provider, usually 30 minutes before meals and at bedtime. Use a proper measuring device to ensure accurate dosing.
Before taking this medication, inform your healthcare provider about all other medications you are taking, as Metoclopramide can interact with certain drugs, potentially altering their effects.
Common side effects may include drowsiness, fatigue, and restlessness. Serious side effects can include involuntary muscle movements, depression, and allergic reactions. Contact your healthcare provider if you experience any severe or concerning symptoms.
Store the suspension at room temperature, away from light and moisture. Keep it out of reach of children and do not freeze the medication.
If you miss a dose, take it as soon as you remember. If it is almost time for your next dose, skip the missed dose and resume your regular dosing schedule. Do not double the dose to catch up.
Consult your healthcare provider before using this medication if you are pregnant or breastfeeding, as it may not be recommended in certain situations.
This medication can be prescribed to children, but the dosage and administration should be carefully determined by a healthcare provider based on the child's specific needs and condition.
In case of an overdose, seek immediate medical attention or contact a poison control center. Symptoms of overdose may include severe drowsiness, confusion, and involuntary muscle movements.
This formulation is compounded by Bayview Pharmacy on a prescriber's order for an individual patient. It is not an FDA-approved drug product, and the FDA has not evaluated it for safety, effectiveness, or manufacturing quality.
A valid prescription is required. Availability depends on Bayview's licensure in your state. This page is general information, not medical advice. Discuss your situation with a licensed healthcare provider.
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Compounded preparations have no NDC, so this formula will not appear in your EHR's drug search. Use your system's compound, non-formulary, or free-text prescription entry and name the preparation exactly as written in step 3. If your EHR forces you to pick a listed drug, pick the closest entry for the active ingredient and put the full formula in the prescription body (the Sig or directions field), not in Notes to Pharmacy.
Compounded preparations have no NDC and will not appear in your drug search. For EPCS to validate, select a drug entry your EHR recognizes as controlled, usually the bulk powder entry for the active ingredient (for example Ketamine (bulk) powder, not a branded product), then put the full formula from step 3 in the prescription body. A free-text entry that does not validate as controlled will be rejected by your EPCS module.
Quantity and directions are starting points for this dose form, not treatment recommendations. Dosing remains the prescriber's responsibility.
Transmit from your EHR. For this non-controlled preparation we also accept fax to (401) 284-4506 and phoned orders at (401) 284-4505. Order forms are on the formulation pages and in the prescriber portal.
Transmit with two-factor authentication through your EPCS-enabled EHR. No order form is offered for this preparation; e-prescribing guides for our controlled preparations are on the formulation pages.
Licensed to dispense in RI, MA, CT, NJ, NH, FL, ME, and PA; New York is served on a limited basis while nonresident registration is pending. Compounded preparations are not FDA-approved. A valid prescription is required. Full guide, including steps by EHR: How to e-prescribe to Bayview. Questions about this formula: call (401) 284-4505.
Take orally