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Bayview Pharmacy's compounded formulation of Ketamine HCl 4%/Ketoprofen 10%/Lidocaine 2% Topical Gel is a semisolid medication dispensed through a pump mechanism. This formulation allows for easy and precise application on the skin, targeting the treatment or absorption of active ingredients. It is primarily used for the management of conditions such as osteoarthritis, rheumatoid arthritis, fibromyalgia, neuropathic pain, and muscle pain.
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 4%/Ketoprofen 10%/Lidocaine 2% Topical Gel is a specially compounded medication designed to provide targeted relief from pain and inflammation associated with various disease states. This unique formulation combines three active ingredients: ketamine hydrochloride, ketoprofen, and lidocaine, each with its own distinct mechanism of action.
Ketamine hydrochloride is an anesthetic that functions by blocking nerve signals in the brain and spinal cord, thereby providing relief from pain. Ketoprofen, a non-steroidal anti-inflammatory drug (NSAID), works by reducing hormones that cause inflammation and pain in the body. Lidocaine, a local anesthetic, operates by blocking nerve signals in the area where it is applied, offering localized relief from pain.
This compounded formulation is indicated for the treatment of pain and inflammation associated with a variety of disease states, including but not limited to arthritis, bursitis, tendonitis, and other musculoskeletal conditions. It can also be effectively used to manage post-surgical pain and inflammation.
The Ketamine HCl 4%/Ketoprofen 10%/Lidocaine 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 active ingredients in a gel-like consistency, providing fast-acting relief from pain and inflammation.
Bayview Pharmacy's Ketamine HCl 4%/Ketoprofen 10%/Lidocaine 2% Topical Gel is a appropriate treatment option for patients suffering from pain and inflammation associated with various disease states. Patients should adhere to their doctor's instructions for use and promptly contact their healthcare provider if they experience any adverse effects.
Healthcare providers should consider this compounded formulation as a viable treatment option for their patients suffering from pain and inflammation associated with various disease states. For any questions or further information about this formulation, please do not hesitate to reach out to us.
This compounded formulation of Ketamine HCl 4%/Ketoprofen 10%/Lidocaine 2% Topical Gel is a semisolid preparation designed for easy and precise application on the skin. It is primarily used for the targeted treatment of pain and inflammation associated with musculoskeletal conditions, as well as the reduction of neuropathic pain symptoms. The formulation combines three active ingredients, each contributing to its overall effectiveness. Lidocaine acts as a local anesthetic, while ketamine and ketoprofen offer anti-inflammatory and analgesic properties.
Patients with a known hypersensitivity to any of the active ingredients are advised not to use this formulation. During use, it is crucial to monitor for potential adverse reactions such as skin irritation, redness, or itching. Should any of these symptoms occur, discontinue use immediately and consult with a healthcare provider. It is also important to avoid contact with the eyes, nose, and mouth to prevent potential irritation.
It is worth noting that this formulation should not be used concurrently with other topical medications, as this may heighten the risk of adverse reactions. Similarly, it should not be used in combination with other medications that may interact with the active ingredients, including anticoagulants, antiplatelet agents, or nonsteroidal anti-inflammatory drugs (NSAIDs).
If you have any questions or concerns regarding this formulation or its use, do not hesitate to seek professional advice. It is always important to use medications responsibly and under the guidance of a healthcare provider.
Ketamine HCl 4%/Ketoprofen 10%/Lidocaine 2% Topical Gel is a compounded formulation that combines the analgesic and anesthetic properties of three active ingredients to provide targeted relief from pain and inflammation.
The formulation contains Ketamine Hydrochloride, an anesthetic that functions by blocking the transmission of pain signals to the brain, thereby reducing the sensation of pain. Ketoprofen, an anti-inflammatory agent, works by inhibiting the production of certain chemicals that cause inflammation. Lidocaine, a local anesthetic, numbs the affected area, further reducing pain and discomfort.
When applied to the skin, this semisolid formulation is dispensed through a pump mechanism, allowing for easy and precise application. The gel-like consistency facilitates quick penetration into the skin, enabling the active ingredients to enter the bloodstream and start working rapidly. This targeted treatment ensures that the active ingredients are delivered directly to the site of pain and inflammation, enhancing their effectiveness.
Ketamine HCl 4%/Ketoprofen 10%/Lidocaine 2% Topical Gel is a appropriate treatment option for pain and inflammation. However, it is crucial to use this medication as directed by your healthcare provider. If you have any questions or concerns about the use of this medication, please consult your doctor or pharmacist.
This compounded formulation of Ketamine HCl 4%/Ketoprofen 10%/Lidocaine 2% Topical Gel is a semisolid preparation that is dispensed through a pump mechanism. This design allows for easy and precise application on the skin, targeting the treatment area directly and facilitating the absorption of active ingredients in a gel-like consistency. This formulation is versatile and may be used to treat a variety of conditions.
It can be used to manage post-operative pain, post-traumatic pain, and chronic pain, providing significant relief. The inclusion of Ketoprofen in the formulation aids in reducing inflammation and swelling associated with these conditions. This formulation also has the potential to lessen the intensity of muscle spasms, providing relief from discomfort.
Additionally, it can be used to alleviate itching and burning sensations, enhancing the comfort of patients. The formulation also has the potential to reduce the risk of infection in wounds and promote healing, contributing to overall patient recovery.
However, patients should be aware that this formulation may cause skin irritation and should be used with caution. If any adverse reactions occur, it is recommended to discontinue use and contact a healthcare provider immediately. Prescribers should also be aware that this formulation may interact with other medications and should be used with caution in patients with a history of allergies or skin sensitivities.
This is a compounded formulation of three active ingredients: Ketamine HCl, Ketoprofen, and Lidocaine. 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 inflammation reduction.
You apply the gel to the affected area of the skin as directed by your healthcare provider. The pump mechanism allows for easy and precise application.
The gel has a semisolid, gel-like consistency. This allows it to be easily spread on the skin and absorbed.
The active ingredients in this gel are Ketamine HCl, Ketoprofen, and Lidocaine. These ingredients work together to manage pain and reduce inflammation.
This gel is intended for external use only. It should be applied to the affected area as directed by your healthcare provider. Avoid contact with eyes, mouth, and other sensitive areas.
The frequency of application will depend on your specific condition and the instructions provided by your healthcare provider. Always follow the prescribed dosage.
If you experience any side effects, such as skin irritation or allergic reactions, stop using the gel and contact your healthcare provider immediately.
If you are pregnant or breastfeeding, you should consult your healthcare provider before using this gel. The active ingredients may have potential effects on the fetus or nursing infant.
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, affecting their effectiveness or causing adverse reactions.
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)
