The Dexamethasone 4 mg/Haloperidol 1 mg/Lorazepam 0.5 mg/Metoclopramide 10 mg/ml Transdermal Gel is a specialized medication designed for the management of symptoms associated with a variety of disease states. This semisolid formulation is dispensed through a pump mechanism, which allows for easy and precise application directly onto the skin.
This transdermal gel is primarily used in the treatment of nausea and vomiting, particularly when associated with cancer chemotherapy and postoperative states. It also serves as an adjunct therapy for managing pain and psychological distress in palliative care settings. The combination of dexamethasone, a corticosteroid, with haloperidol, an antipsychotic, lorazepam, a benzodiazepine, and metoclopramide, a prokinetic and antiemetic agent, provides a multimodal approach to symptom control. This can be especially beneficial in patients experiencing multiple concurrent symptoms that require complex management strategies.

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.
Our custom-compounded transdermal gel combines four active ingredients: Dexamethasone, Haloperidol, Lorazepam, and Metoclopramide, each serving a unique purpose in patient care. Dexamethasone is a potent corticosteroid that helps reduce inflammation and modulate immune responses, making it useful in treating various inflammatory and autoimmune conditions. Lorazepam, a benzodiazepine, is included for its anxiolytic and sedative properties, which can be beneficial in treating anxiety disorders and providing sedation for agitated patients. Metoclopramide, a prokinetic and antiemetic agent, is particularly useful in treating gastroparesis and refractory nausea in various clinical scenarios.
The formulation is designed as a semisolid gel for transdermal delivery, allowing for systemic absorption of the medications through the skin. This route of administration can be advantageous for patients who have difficulties with oral intake or require a steady release of medication into the bloodstream. The gel is dispensed through a pump mechanism, which ensures consistent dosing and ease of use. The transdermal application also minimizes gastrointestinal side effects and bypasses first-pass metabolism, potentially reducing the risk of drug interactions and enhancing therapeutic efficacy.
This multi-drug transdermal gel is particularly suited for patients with complex medical needs, such as those with cancer, hospice patients, or those with severe psychiatric symptoms accompanied by nausea or vomiting. It can provide symptomatic relief from nausea, vomiting, anxiety, agitation, and inflammatory conditions, all within one formulation. The combination of these four drugs in a single transdermal gel allows for a multimodal approach to treatment, which can be tailored to individual patient needs.
For prescribers considering this formulation, it is important to assess each patient's medical history, current medications, and potential for drug interactions. Monitoring for side effects, especially with long-term use, is crucial due to the systemic effects of the corticosteroid and the potential for sedation or extrapyramidal symptoms with the antipsychotic and benzodiazepine components. As compounding pharmacists, we are available to discuss the suitability of this formulation for specific patients, provide dosing recommendations, and offer guidance on monitoring parameters.
Patients should be counseled on the proper application of the gel, the importance of adhering to prescribed dosing schedules, and the need to report any adverse effects promptly. It is also essential to store the medication as directed to maintain its efficacy and stability. If you have any questions or require further information about this transdermal gel formulation, please reach out to us at Bayview Pharmacy. Our team is committed to providing comprehensive support to both patients and healthcare providers.
The combination of dexamethasone, haloperidol, lorazepam, and metoclopramide in a transdermal gel formulation presents a unique profile of potential drug interactions that must be carefully considered. Dexamethasone is a corticosteroid that can interact with drugs such as nonsteroidal anti-inflammatory drugs (NSAIDs), leading to an increased risk of gastrointestinal ulcers or bleeding. It may also reduce the efficacy of diabetes medications due to its hyperglycemic effect. Additionally, dexamethasone can induce the metabolism of certain drugs, potentially decreasing their effectiveness, including medications like warfarin, which could lead to a reduced anticoagulant effect.
Haloperidol, an antipsychotic, can interact with drugs that prolong the QT interval, increasing the risk of cardiac arrhythmias. Caution is advised when co-administered with other QT-prolonging drugs such as certain antiarrhythmics, macrolide antibiotics, and some antidepressants. Haloperidol can also potentiate the effects of CNS depressants, including opioids, sedatives, and anxiolytics, which could lead to increased sedation and respiratory depression.
Lorazepam, a benzodiazepine, similarly can cause additive CNS depression when used with other CNS depressants. This can result in enhanced sedation, dizziness, and impaired motor coordination. Additionally, lorazepam's metabolism may be affected by inhibitors of cytochrome P450 enzymes, particularly CYP3A4, potentially leading to increased plasma levels and toxicity.
Metoclopramide, a prokinetic and antiemetic agent, can interact with drugs that are dopamine antagonists, potentially leading to an increased risk of extrapyramidal symptoms. It may also enhance the absorption of other drugs by increasing gastrointestinal motility, which could alter the effects of concomitantly administered medications. Furthermore, metoclopramide's efficacy can be reduced by anticholinergic drugs, as they may counteract its prokinetic effects.
It is important to note that the transdermal route of administration may alter the interaction profile of these medications compared to oral administration. However, systemic absorption and the potential for interactions still exist. This formulation is used to treat various conditions, including nausea, vomiting, anxiety, agitation, and inflammatory conditions, by providing a combination of antiemetic, anxiolytic, antipsychotic, and anti-inflammatory effects. Due to the complexity of this formulation, it is crucial for prescribers to review the patient's complete medication profile for potential interactions and adjust therapy accordingly. Patients should be monitored for signs of adverse effects, and dose adjustments may be necessary. If you have any questions or require further information regarding this formulation and its potential drug interactions, please reach out to us at Bayview Pharmacy.
The transdermal gel formulation containing Dexamethasone, Haloperidol, Lorazepam, and Metoclopramide is designed to deliver medication directly through the skin into the bloodstream. This method of delivery is particularly useful for patients who may have difficulties with oral administration or where bypassing the gastrointestinal tract is preferred. The gel is a semisolid dosage form that allows for the active ingredients to be dissolved or suspended in a suitable base, which facilitates the penetration of the medication through the skin barrier.
Dexamethasone is a potent corticosteroid with anti-inflammatory and immunosuppressant properties. In this transdermal formulation, it can be used to reduce inflammation and modulate the body's immune response. This can be beneficial in treating localized inflammatory conditions or in palliative care settings to alleviate specific symptoms such as swelling, pain, or allergic reactions.
Haloperidol is an antipsychotic medication that can help manage symptoms of acute agitation or delirium. When administered transdermally, it can provide a more consistent delivery of medication, which may be advantageous in managing chronic symptoms or in situations where oral administration is compromised.
Lorazepam is a benzodiazepine that exerts anxiolytic, sedative, and muscle relaxant effects. In a transdermal gel, Lorazepam can be used to alleviate anxiety, promote relaxation, and help with sleep disturbances. The transdermal route allows for steady absorption, which can help maintain therapeutic levels of the drug without the peaks and troughs associated with oral administration.
Metoclopramide is a medication that acts as an antiemetic and a prokinetic agent. It is often used to prevent nausea and vomiting, as well as to facilitate gastric emptying. By incorporating Metoclopramide into a transdermal gel, patients who are unable to take oral medications due to vomiting or gastric stasis can still receive the therapeutic benefits of the drug.
The combination of these four medications in a transdermal gel allows for a multimodal approach to symptom management, particularly in palliative care, where patients may suffer from a complex array of symptoms. The gel is dispensed through a pump mechanism, which ensures that a precise dose is administered each time. The gel-like consistency makes it easy to apply and allows for targeted treatment, as the medication can be applied directly to the area of discomfort or where absorption is desired.
It is important for both patients and prescribers to understand the pharmacokinetics and dynamics of each component in the formulation, as well as the potential interactions and side effects. Monitoring and adjusting the dose may be necessary to achieve the desired therapeutic effect while minimizing adverse reactions. If you have any questions or require further information about this transdermal gel formulation, please reach out to us at Bayview Pharmacy. Our team of compounding pharmacists is here to provide guidance and support.
This compounded transdermal gel is typically used to manage symptoms such as nausea, vomiting, agitation, anxiety, and pain, especially in a palliative care setting. It delivers a combination of Dexamethasone, Haloperidol, Lorazepam, and Metoclopramide through the skin to target these symptoms.
To use this gel, pump the prescribed amount onto your finger or directly onto the skin and apply it to an area of skin that is clean and hair-free. Common sites for application include the inner wrist or upper chest. Rub it in gently until it's fully absorbed.
The frequency of application will be determined by your healthcare professional based on your individual needs. It's important to follow their instructions and not to exceed the recommended dosage.
If you miss a dose of the gel, apply it as soon as you remember. However, 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.
As with any medication, side effects are possible. Common side effects can include skin irritation at the application site, drowsiness, and dry mouth. If you experience severe reactions or side effects that concern you, contact your healthcare provider immediately.
Generally, it is not necessary to cover the application site with a bandage. The gel is designed to be absorbed into the skin without the need for occlusive dressings. Consult with your healthcare provider if you believe covering the site is necessary.
Because this gel can cause drowsiness due to the presence of Lorazepam, it's important to avoid activities that require alertness, such as driving or operating heavy machinery, until you know how the medication affects you.
Store the transdermal gel at room temperature, away from heat and direct light. Do not freeze, and keep the container tightly closed when not in use. Keep it out of reach of children and pets.
If someone accidentally ingests this transdermal gel, seek emergency medical attention immediately or call a poison control center. It contains active ingredients that could be harmful if taken orally.
After applying the gel, you should wait for at least an hour to allow the medication to be absorbed. Avoid taking a shower, bathing, or swimming during this time to ensure the effectiveness of the treatment.
You may notice an improvement in your symptoms such as reduced nausea, agitation, or pain. It's important to keep track of your symptoms and report any significant changes to your healthcare provider to assess the effectiveness of your treatment.
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.
This preparation is a controlled substance. Additional prescribing, refill, and shipping restrictions apply, and the states Bayview can dispense it to are narrower than for non-controlled preparations.
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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.
Apply topically to affected area(s)