The Imatinib 50 mg/ml Gastric Tube Liquid is a specially compounded medication intended for administration through a gastric tube. This formulation is designed to provide a precise dosage of imatinib, which is critical for the treatment of certain types of cancer. Imatinib is a targeted therapy used to treat chronic myeloid leukemia (CML) and gastrointestinal stromal tumors (GISTs), as well as other malignancies that are characterized by the presence of specific genetic mutations. The liquid form ensures that patients who are unable to swallow pills, such as those with dysphagia or who are receiving care in a hospital setting, can still receive their necessary medication safely and effectively.

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.
Imatinib 50 mg/ml Gastric Tube Liquid is a specially compounded medication designed for administration through a gastric tube, providing an alternative route of administration for patients who are unable to take oral medications. This includes individuals with swallowing difficulties, those who are unconscious or on mechanical ventilation, and patients with conditions that impair the swallowing reflex or gastrointestinal motility. The liquid formulation ensures that the active ingredient, imatinib, is delivered in a precise and controlled manner, which is critical for maintaining therapeutic drug levels and optimizing treatment efficacy.
Imatinib is a tyrosine kinase inhibitor that is primarily used in the treatment of certain types of cancer, including chronic myeloid leukemia (CML) and gastrointestinal stromal tumors (GISTs). It works by selectively inhibiting the Bcr-Abl tyrosine kinase, an abnormal enzyme produced by cancer cells in CML. This inhibition blocks the proliferation and induces apoptosis of the leukemic cells. In GISTs, imatinib targets the KIT protein and platelet-derived growth factor receptors (PDGFR), which are often mutated and overactive, leading to tumor growth. By blocking these receptors, imatinib can cause tumor cells to die or stop growing.
The compounding of Imatinib 50 mg/ml Gastric Tube Liquid requires meticulous attention to detail to ensure stability, sterility, and the correct concentration of the active ingredient. The formulation is prepared in a controlled environment to prevent contamination and degradation of the medication. It is important for prescribers to be aware that the bioavailability of the liquid formulation may differ from that of the standard oral tablet, and dosing adjustments may be necessary to achieve the desired therapeutic effect.
Patients and caregivers should be instructed on the proper administration techniques for gastric tube medications to ensure safety and effectiveness. This includes checking the placement of the gastric tube, flushing the tube before and after medication administration, and understanding the importance of proper storage and handling of the liquid medication. Monitoring for potential side effects, such as nausea, vomiting, edema, muscle cramps, and rash, is also essential, as is regular blood work to monitor the patient's response to therapy.
For those interested in using Imatinib 50 mg/ml Gastric Tube Liquid, it is crucial to consult with a healthcare professional to determine the appropriateness of this formulation for the patient's specific condition and needs. Our team at Bayview Pharmacy is available to answer any questions and provide additional information to both patients and prescribers regarding this specialized medication. Do not hesitate to reach out to us for guidance and support in managing your or your patient's treatment with Imatinib 50 mg/ml Gastric Tube Liquid.
Imatinib is a tyrosine kinase inhibitor that is primarily used in the treatment of certain types of cancer, such as chronic myeloid leukemia (CML) and gastrointestinal stromal tumors (GISTs). When administered as a 50 mg/ml gastric tube liquid, it is important to consider potential drug interactions that may affect its efficacy and safety.
Imatinib is metabolized mainly by the CYP3A4 enzyme system in the liver. Therefore, concomitant use with strong CYP3A4 inhibitors (such as ketoconazole, itraconazole, clarithromycin, atazanavir, nefazodone) can increase imatinib plasma concentrations, potentially leading to increased toxicity. Conversely, co-administration with strong CYP3A4 inducers (such as rifampicin, phenytoin, carbamazepine, St. John's Wort) may decrease imatinib plasma concentrations, reducing its therapeutic effect. Caution and close monitoring are advised when imatinib is used with these agents.
Imatinib can also affect the metabolism of drugs that are substrates of CYP3A4, CYP2D6, CYP2C9, and CYP2C19. This means that imatinib has the potential to increase plasma concentrations of these drugs, which could enhance or prolong both therapeutic and adverse effects. For example, if imatinib is taken with certain cholesterol-lowering medications (statins), blood thinners (warfarin), or antidepressants (selective serotonin reuptake inhibitors), monitoring for increased effects or toxicity of these drugs may be necessary.
Proton pump inhibitors (PPIs) and H2 blockers, which are commonly used to manage gastrointestinal side effects, may decrease the solubility of imatinib and thus reduce its bioavailability when administered via a gastric tube. If these medications are necessary, consider administering them at different times to minimize the interaction.
Additionally, imatinib has been reported to interact with acetaminophen, which may increase the risk of hepatotoxicity. Patients should be advised to use acetaminophen cautiously and under medical supervision, especially if long-term use is anticipated.
It is also important to note that imatinib can have an additive effect with other drugs that prolong the QT interval, which can increase the risk of serious cardiac arrhythmias. Patients should be monitored for signs and symptoms of cardiac arrhythmias, and the use of other QT-prolonging drugs should be carefully considered.
Lastly, imatinib may interact with grapefruit juice, which can inhibit CYP3A4 and lead to increased plasma levels of imatinib. Patients should be advised to avoid grapefruit juice while taking imatinib.
Due to the complexity and potential severity of drug interactions with imatinib, it is crucial for prescribers to review all medications that a patient is taking before initiating treatment with imatinib. Pharmacists should verify the patient's medication history and provide counseling on potential interactions. For any questions or concerns regarding drug interactions with imatinib 50 mg/ml gastric tube liquid, please reach out to us at Bayview Pharmacy for further assistance.
The Imatinib 50 mg/ml Gastric Tube Liquid is a specially compounded formulation designed to facilitate the administration of imatinib, a tyrosine kinase inhibitor, through a gastric tube. This delivery method is particularly beneficial for patients who are unable to swallow oral medications due to various medical conditions. Imatinib, the active ingredient in this formulation, works by selectively inhibiting specific tyrosine kinases, which are enzymes that play a crucial role in the signaling pathways that regulate cell growth and survival.
In the treatment of certain types of cancer, such as chronic myeloid leukemia (CML) and gastrointestinal stromal tumors (GISTs), the BCR-ABL tyrosine kinase is produced by cancer cells due to a chromosomal abnormality. Imatinib binds to this abnormal kinase, thereby inhibiting its activity and preventing the cancer cells from proliferating. This targeted approach allows for the management of these diseases by directly interfering with the growth and spread of cancer cells while minimizing the impact on healthy cells.
The liquid formulation of imatinib is specifically designed to maintain the stability and solubility of the drug, ensuring that the correct dosage is delivered through the gastric tube. This is critical for maintaining the therapeutic effectiveness of the medication. The compounding process involves dissolving imatinib mesylate in a suitable solvent system, which may include a combination of water, alcohol, and other non-toxic solvents, along with flavoring agents to mask any unpleasant tastes should any residue remain in the mouth.
It is important for prescribers to consider the pharmacokinetic properties of imatinib when prescribing this formulation. The liquid form ensures that the drug is readily available for absorption in the stomach and the proximal intestine, which is essential for achieving the desired therapeutic effect. Additionally, the liquid formulation can be easily adjusted to meet the specific dosage requirements of individual patients, which is particularly important given the variability in the response to imatinib among patients with different genetic profiles and disease states.
For patients and prescribers interested in using the Imatinib 50 mg/ml Gastric Tube Liquid formulation, it is essential to understand that this medication should be used under the guidance of a healthcare professional experienced in the treatment of the relevant cancer types. If you have any questions or require further information about this formulation, please reach out to us at Bayview Pharmacy. Our team of compounding pharmacists is committed to providing the highest quality of care and is available to assist with any inquiries regarding the preparation, administration, and pharmacological aspects of this medication.
Imatinib 50 mg/ml Gastric Tube Liquid is a specially compounded formulation of the medication Imatinib, prepared at a concentration of 50 mg per milliliter. It is designed specifically for administration through a gastric tube for patients who are unable to swallow oral medications.
This medication is delivered directly into the stomach through a gastric tube. Appropriate measures must be taken to ensure the tube is properly placed and the medication is administered correctly and safely, following the healthcare provider's instructions.
While it provides a safe alternative for patients with swallowing difficulties or those who cannot take oral medications, not all patients may be suited for this form of Imatinib. It should only be used after a healthcare provider has assessed its suitability for an individual patient's needs.
Yes, the dosage can be adjusted by a healthcare professional according to the patient's individual requirements, the response to treatment, and any other concurrent medications or medical conditions.
Imatinib Gastric Tube Liquid should be stored at room temperature away from light and moisture, unless otherwise specified by the pharmacist. It’s important to keep this medication out of reach of children and pets.
As with any medication, there may be potential side effects. These can range from mild to severe and may include but are not limited to nausea, vomiting, diarrhea, fatigue, and muscle cramps. Any side effects should be reported to a healthcare provider immediately.
Imatinib Gastric Tube Liquid should not be mixed with other liquids or foods unless advised by a healthcare provider. Mixing the medication can affect its efficacy and could cause adverse reactions.
The onset of action for Imatinib Gastric Tube Liquid can vary depending on the patient's specific condition and metabolism. It's important to regularly monitor therapeutic response and side effects under the guidance of a healthcare provider.
If a dose is missed, it should be taken as soon as possible. However, if it is near the time for the next dose, the missed dose should be skipped, and the regular dosing schedule should be resumed. Do not double the dose to catch up unless advised by a healthcare provider.
In the case of a suspected overdose, seek immediate medical attention. Overdose symptoms may include severe side effects or toxic reactions, and prompt medical intervention is critical.
Yes, Imatinib Gastric Tube Liquid can interact with other medications, which may affect how it works or increase the risk of serious side effects. Always inform the healthcare provider of all medications and supplements the patient is using before starting treatment with Imatinib Gastric Tube Liquid.
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.
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.