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Hydromorphone 10 mg/mL Intravenous Infusion

Hydromorphone 10 mg/mL Intravenous Infusion is a compounded medication delivered through a sterile intravenous bag, designed for precise and controlled administration directly into the bloodstream.

This formulation is specifically tailored for effective pain management, addressing various conditions such as cancer pain, postoperative pain, chronic pain, and palliative care. It is particularly utilized in end-of-life hospice care to ensure patient comfort and quality of life.

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Formula Information

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Hydromorphone 10 mg/mL Intravenous Infusion is a potent opioid analgesic formulation designed for the management of severe pain, particularly in cases where alternative treatments are inadequate. This formulation is delivered via an intravenous bag, a sterile container that ensures the medication is administered directly into the patient's bloodstream. This method of delivery allows for rapid onset of action and precise control over dosing, making it an ideal choice for managing acute and chronic pain conditions.

In the context of pain management, hydromorphone is particularly effective due to its high potency and efficacy in alleviating severe pain. It is commonly used in cancer pain management, where patients may experience intense and persistent pain that requires strong analgesics. The intravenous route is especially beneficial in this setting, as it provides immediate relief and can be adjusted quickly to meet the patient's changing needs.

For postoperative pain, hydromorphone offers significant benefits by reducing the discomfort associated with surgical procedures. Its ability to provide consistent and controlled pain relief helps improve patient recovery times and overall comfort during the postoperative period. In chronic pain management, hydromorphone is used when other pain relief measures are insufficient, offering patients a viable option to manage their symptoms effectively.

In palliative care and end-of-life hospice care, hydromorphone plays a crucial role in ensuring patient comfort. It addresses the complex pain needs of patients with terminal illnesses, allowing them to maintain a better quality of life during their remaining time. The formulation's flexibility in dosing and rapid action make it a preferred choice for healthcare providers aiming to deliver compassionate and effective care.

For both patients and prescribers, it is important to understand the potential side effects and risks associated with hydromorphone use, including respiratory depression, sedation, and the potential for dependence. Close monitoring and appropriate dosing adjustments are essential to minimize these risks and ensure safe and effective pain management.

If you have any questions or require further information about this formulation, please reach out to us at Bayview Pharmacy. Our team of knowledgeable compounding pharmacists is here to assist you with any inquiries or concerns you may have.

Drug Interactions

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Hydromorphone 10 mg/mL intravenous infusion is a potent opioid analgesic used in the management of severe pain, including pain associated with cancer, postoperative recovery, chronic conditions, and palliative care, particularly in end-of-life hospice settings. While effective in providing relief, it is crucial to be aware of potential drug interactions that may affect the safety and efficacy of this formulation.

Concomitant use of hydromorphone with other central nervous system (CNS) depressants, such as benzodiazepines, barbiturates, other opioids, or alcohol, can result in additive CNS depression. This may lead to profound sedation, respiratory depression, coma, or even death. It is essential for prescribers to evaluate the patient's medication regimen and consider dose adjustments or alternative therapies to mitigate these risks.

Hydromorphone is metabolized primarily by the liver enzyme CYP3A4. Co-administration with drugs that inhibit CYP3A4, such as certain antifungals (e.g., ketoconazole), macrolide antibiotics (e.g., erythromycin), or protease inhibitors (e.g., ritonavir), can increase hydromorphone plasma concentrations, potentially leading to enhanced effects and toxicity. Conversely, CYP3A4 inducers, such as rifampin, carbamazepine, or phenytoin, may decrease hydromorphone levels, reducing its analgesic efficacy. Monitoring and possible dose adjustments are recommended when these agents are used concurrently.

Patients taking monoamine oxidase inhibitors (MAOIs) or those who have recently discontinued MAOIs should avoid hydromorphone due to the risk of serotonin syndrome, a potentially life-threatening condition characterized by symptoms such as agitation, hallucinations, rapid heart rate, and increased body temperature. A washout period of at least 14 days is generally advised before initiating hydromorphone in patients previously treated with MAOIs.

In patients receiving diuretics, hydromorphone may reduce the efficacy of these medications by inducing the release of antidiuretic hormone, leading to fluid retention and potential exacerbation of conditions such as heart failure. Close monitoring of fluid status and renal function is advised in such cases.

For patients on anticoagulant therapy, particularly those on warfarin, there is a potential for hydromorphone to alter the anticoagulant effects, necessitating more frequent monitoring of INR levels to ensure therapeutic anticoagulation without increased risk of bleeding.

It is important for both patients and prescribers to be aware of these potential interactions and to communicate openly about all medications being taken, including over-the-counter drugs and supplements. If you have any questions or need further information, please reach out to us at Bayview Pharmacy. We are here to assist you in ensuring safe and effective pain management for your patients.

How Does it Work

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Hydromorphone 10 mg/mL Intravenous Infusion is a potent opioid analgesic formulation designed for direct administration into the bloodstream, ensuring rapid and effective pain relief. This formulation is particularly beneficial in managing severe pain conditions, including cancer pain, postoperative pain, chronic pain, and pain associated with palliative and end-of-life hospice care. By delivering hydromorphone intravenously, the medication bypasses the gastrointestinal tract, allowing for immediate onset of action, which is crucial for patients requiring urgent pain management.

In the context of pain management, hydromorphone works by binding to the mu-opioid receptors in the central nervous system. This binding alters the perception of pain and the emotional response to it, providing significant relief to patients experiencing severe discomfort. For cancer pain, which can be persistent and intense, hydromorphone offers a reliable option to improve quality of life by reducing pain levels and allowing patients to engage more comfortably in daily activities.

Postoperative pain can vary in intensity and duration, and hydromorphone's intravenous administration allows for precise control over dosing, ensuring that patients receive the exact amount needed to manage their pain effectively. This precision is particularly important in a postoperative setting, where pain levels can fluctuate significantly.

For those suffering from chronic pain, hydromorphone provides a consistent and reliable method of pain control, helping to manage symptoms that may not respond well to other forms of treatment. Its use in palliative care and end-of-life hospice care is especially critical, as it helps to alleviate severe pain, allowing patients to focus on comfort and quality of life during their final days.

The intravenous bag used for this formulation is a sterile container that ensures the safe and effective delivery of hydromorphone directly into the patient's bloodstream. This method of administration allows healthcare providers to adjust dosages quickly and accurately, tailoring treatment to the individual needs of each patient. The controlled delivery system minimizes the risk of overdose and side effects, providing a safer option for managing severe pain.

For prescribers, it is essential to consider the patient's overall health status, potential for opioid tolerance, and any previous history of opioid use when determining the appropriate dosage of hydromorphone. Close monitoring is necessary to ensure optimal pain management while minimizing the risk of adverse effects. Patients and caregivers should be educated on the potential side effects of hydromorphone, which may include drowsiness, dizziness, nausea, and constipation, and should be advised to report any concerning symptoms to their healthcare provider promptly.

If you have any questions or require further information about Hydromorphone 10 mg/mL Intravenous Infusion, 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 and its use in pain management.

Other Uses

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Hydromorphone 10 mg/mL intravenous infusion is primarily used for its potent analgesic properties in managing various types of pain, such as cancer pain, postoperative pain, chronic pain, and in palliative care settings. However, beyond these primary indications, there are other potential therapeutic uses for this formulation, particularly within specialized clinical contexts. Alternative uses include its role in managing severe dyspnea in patients with advanced respiratory diseases, addressing debilitating symptoms such as shortness of breath that are often seen in end-stage chronic obstructive pulmonary disease (COPD) and pulmonary fibrosis. In such cases, hydromorphone can improve the quality of life by alleviating respiratory distress, making it a valuable option within palliative respiratory care.

Additionally, hydromorphone can be utilized in certain instances of complex regional pain syndrome (CRPS), where traditional pain management strategies may not suffice. Its use in CRPS involves attempting to provide relief where other opioids or neuropathic pain agents may have limited effectiveness. Moreover, its application extends to severe sickle cell crisis episodes, where managing excruciating vaso-occlusive episodes can significantly benefit from its potent analgesic effects. These alternative uses necessitate careful consideration and monitoring by healthcare providers due to the formulation's potency and potential side effects.

Importantly, hydromorphone intravenous infusion can sometimes be employed off-label in situations involving severe renal colic, providing rapid relief during acute episodes. In patients experiencing refractory pain unresponsive to other treatments, this formulation's rapid onset can be especially beneficial. While its primary applications lie in significant pain management scenarios, exploring these other uses requires a comprehensive understanding by prescribers of a patient's specific medical condition and history, ensuring that the risks are managed appropriately.

For patients and healthcare providers considering alternative applications of hydromorphone 10 mg/mL intravenous infusion beyond routine pain management, it is vital to consult with specialized compounding pharmacists and healthcare professionals who can tailor therapy regimens to suit individual needs safely and effectively. If you have any questions or require further clarification on the uses and administration of this formulation, please reach out to us at Bayview Pharmacy. Our team is dedicated to providing expert guidance and support to optimize therapeutic outcomes while maintaining patient safety.

Frequently Asked Questions

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What is Hydromorphone 10 mg/mL Intravenous Infusion used for?

This formulation is primarily used in end-of-life hospice care for pain management. It provides relief from severe pain, ensuring comfort for patients in their final stages of life.

How is this medication administered?

The medication is administered using a sterile intravenous (IV) bag that delivers the compounded formulation directly into the patient's bloodstream, ensuring precise and controlled treatment.

What are the benefits of using an intravenous infusion for this medication?

Intravenous infusion allows for immediate effect, accurate dosage control, and rapid pain relief by delivering medication directly into the bloodstream.

Who should administer Hydromorphone 10 mg/mL Intravenous Infusion?

This medication should only be administered by healthcare professionals who are trained in delivering IV medications and managing patients in hospice care.

Can this formulation be stored for future use?

Hydromorphone 10 mg/mL Intravenous Infusion should be stored as advised by the compounding pharmacy and used within the recommended timeframe to ensure its effectiveness and sterility.

What should caregivers expect in terms of pain relief for the patient?

Caregivers can expect significant pain relief for the patient, enhancing comfort during the end-of-life process. Healthcare providers will adjust doses as needed.

Are there any side effects associated with this medication?

Possible side effects include drowsiness, constipation, nausea, and dizziness. Healthcare providers will monitor the patient for any adverse effects and manage them accordingly.

How is the appropriate dosage determined for each patient?

The dosage is customized based on the patient's specific needs, including the severity of pain and the patient's medical history, which is assessed by healthcare professionals.

What precautions should be taken during administration?

Ensure the infusion is prepared and checked by qualified personnel, monitor the infusion site for irritation, and observe the patient closely for any adverse reactions.

What should be done in case of an overdose?

If an overdose is suspected, it is critical to seek emergency medical help immediately. Supportive measures and treatments, such as naloxone, may be necessary to manage symptoms.

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Formulas and/or material listed are not to be interpreted as a promise, guarantee or claim of therapeutic efficacy or safety. The information contained herein is not intended to replace or substitute for conventional medical care, or encourage its abandonment. Every patient is unique, and formulas should be adjusted to meet their individual needs.

No compounded medications are reviewed by the FDA for safety or efficacy.