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Bayview Pharmacy's Ketamine HCl 7.5%/Gabapentin 10%/Baclofen 2% Topical Gel is a semisolid formulation dispensed through a pump mechanism. This allows for easy and precise application on the skin, facilitating targeted treatment or absorption of active ingredients. The gel-like consistency of this compounded medication is used to treat conditions such as neuropathic pain, spasticity, fibromyalgia, migraine, and trigeminal neuralgia.
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.
Bayview Pharmacy's Ketamine HCl 7.5%/Gabapentin 10%/Baclofen 2% Topical Gel is a specially compounded medication designed to address a range of chronic pain conditions.
Gabapentin, an anticonvulsant, has shown positive results in managing neuropathic pain, trigeminal neuralgia, and fibromyalgia.
This compounded formulation is designed to provide targeted relief from chronic pain conditions by addressing multiple pain pathways. The synergistic combination of ketamine hydrochloride, gabapentin, and baclofen has been found to significantly reduce pain and improve the quality of life in patients suffering from neuropathic pain, spasticity, fibromyalgia, trigeminal neuralgia, and complex regional pain syndrome.
The Ketamine HCl 7.5%/Gabapentin 10%/Baclofen 2% Topical Gel is dispensed through a pump mechanism, facilitating easy and precise application on the skin. This semisolid formulation allows for targeted treatment or absorption of the active ingredients in a gel-like consistency, providing patients with a convenient and effective method of pain management.
Bayview Pharmacy's Ketamine HCl 7.5%/Gabapentin 10%/Baclofen 2% Topical Gel is a appropriate treatment option for patients suffering from chronic pain conditions. We are committed to providing high-quality compounded medications to meet the unique needs of our patients. If you have any questions about this formulation or would like to learn more, please do not hesitate to reach out to us.
Interactions between the compounded formulation of Ketamine HCl 7.5%/Gabapentin 10%/Baclofen 2% Topical Gel and other medications have not been extensively studied. It is crucial for patients to inform their healthcare provider of all medications they are currently taking, including over-the-counter medications, vitamins, and herbal supplements.
This topical gel is indicated for the treatment of neuropathic pain, spasticity, fibromyalgia, trigeminal neuralgia, and complex regional pain syndrome. It is believed to function by blocking the transmission of pain signals to the brain and reducing inflammation.
Potential interactions may occur with other medications, including anticonvulsants, antidepressants, and muscle relaxants. Patients should inform their healthcare provider if they are taking any of these medications.
The Ketamine HCl 7.5%/Gabapentin 10%/Baclofen 2% Topical Gel may also interact with certain supplements, such as omega-3 fatty acids, vitamin B12, and magnesium. Patients should inform their healthcare provider if they are taking any of these supplements.
There may also be interactions with certain foods, such as dairy products, caffeine, and alcohol. Patients should inform their healthcare provider if they are consuming any of these foods.
Furthermore, the topical gel may interact with certain medical conditions, such as kidney or liver disease, heart disease, or diabetes. Patients should inform their healthcare provider if they have any of these conditions.
If you have any questions about the interactions between the compounded formulation of Ketamine HCl 7.5%/Gabapentin 10%/Baclofen 2% Topical Gel and other medications, supplements, foods, or medical conditions, please consult with your healthcare provider.
Ketamine HCl 7.5%/Gabapentin 10%/Baclofen 2% Topical Gel is a specially compounded medication designed to address various chronic pain conditions. These conditions may include neuropathic pain, spasticity, fibromyalgia, trigeminal neuralgia, and complex regional pain syndrome. The gel is applied directly to the skin of the affected area, providing targeted treatment by blocking the transmission of pain signals to the brain.
The formulation contains three active ingredients: Ketamine HCl, Gabapentin, and Baclofen. Ketamine HCl is an anesthetic that functions by blocking the NMDA receptor, a key player in transmitting pain signals. Gabapentin, an anticonvulsant, works by inhibiting the release of neurotransmitters that cause pain. Baclofen, a muscle relaxant, operates by blocking the release of neurotransmitters that trigger muscle spasms. The combined effect of these medications helps to alleviate pain and spasticity in the affected area.
Patients are advised to apply the gel to the affected area twice daily or as directed by their healthcare provider. It is crucial to adhere to the instructions on the label and avoid contact with the eyes, nose, and mouth. In case of accidental contact with the eyes, rinse thoroughly with water for 15 minutes. If irritation or redness occurs, discontinue use and consult your healthcare provider immediately.
Healthcare providers should closely monitor patients for any signs of adverse reactions, such as skin irritation, redness, or burning. If any of these symptoms occur, the patient should stop using the gel and contact their healthcare provider. Additionally, patients should be observed for signs of an allergic reaction, such as hives, difficulty breathing, or swelling of the face, lips, tongue, or throat.
If you have any questions or concerns about the Ketamine HCl 7.5%/Gabapentin 10%/Baclofen 2% Topical Gel or its mechanism of action, please do not hesitate to reach out to your healthcare provider or pharmacist.
This compounded formulation of Ketamine HCl 7.5%, Gabapentin 10%, and Baclofen 2% is presented in a topical gel format. It is a semisolid formulation that is dispensed through a pump mechanism, which allows for easy and precise application on the skin. The gel-like consistency aids in the targeted treatment or absorption of the active ingredients.
Traditionally, this formulation has been used in the management of Neuropathic Pain, Spasticity, Fibromyalgia, Migraine, and Trigeminal Neuralgia. However, it may also be beneficial in treating other conditions such as chronic pain, muscle spasms, and nerve pain. It is crucial to consult a healthcare provider before using this formulation for any condition not listed above.
Patients should not use this formulation in combination with other topical medications or products without first consulting a healthcare provider. It is also important to note that this formulation may cause skin irritation in some individuals. Therefore, it should be used with caution. If any adverse reactions occur, such as redness, itching, or swelling, discontinue use immediately and contact your healthcare provider.
Always remember to use this medication as directed by your healthcare provider. If you have any questions or concerns about the use of this formulation, do not hesitate to contact your healthcare provider for further information and guidance.
This is a compounded formulation of three active ingredients: Ketamine HCl, Gabapentin, and Baclofen. It is a semisolid formulation that is dispensed through a pump mechanism for easy and precise application on the skin.
The purpose of this topical gel is to provide targeted treatment or absorption of the active ingredients. It is typically used for pain management and muscle relaxation.
This gel should be applied directly to the skin in the area where treatment is needed. The pump mechanism allows for easy and precise application.
The consistency of this gel is semisolid, similar to a gel-like consistency. This allows it to be easily spread on the skin for optimal absorption.
It is recommended to use this gel only on the area where treatment is needed. Avoid contact with eyes, mouth, and other sensitive areas. Always follow your healthcare provider's instructions.
The active ingredients in this gel are Ketamine HCl 7.5%, Gabapentin 10%, and Baclofen 2%.
If you experience any side effects, stop using the gel and contact your healthcare provider immediately.
This gel should be stored at room temperature, away from heat and direct light. Keep it out of reach of children and pets.
If you are pregnant or breastfeeding, consult your healthcare provider before using this gel. The active ingredients may have potential effects on the baby.
Before using this gel, inform your healthcare provider about any other medications you are currently taking. Some medications may interact with the active ingredients in this gel.
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.
The conditions listed on this page are indications prescribers have ordered this preparation for. They are not FDA-approved indications, and listing them is not a statement that this preparation is effective for them.
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.
Search by NCPDP 4106882, or by name and ZIP: Bayview Pharmacy, Warwick, RI 02886. Select it as the destination pharmacy and save it as a favorite. Click any value to copy it.
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)
