Apomorphine 30 mg/mL Oral Suspension is a liquid dosage form in which apomorphine is uniformly dispersed throughout a liquid medium, ensuring a homogeneous mixture for administration. This formulation is primarily used in the management of Parkinson's disease, providing symptomatic relief from motor fluctuations and "off" episodes.

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.
Apomorphine 30 mg/mL Oral Suspension is a compounded medication formulated to provide an alternative route of administration for patients requiring apomorphine therapy. This liquid dosage form ensures that the active ingredient, apomorphine, is uniformly dispersed throughout the liquid medium, resulting in a homogeneous mixture that allows for accurate and consistent dosing.
Apomorphine is a potent dopamine agonist used primarily in the management of Parkinson's disease, specifically for the treatment of "off" episodes in patients experiencing motor fluctuations. These episodes are characterized by a sudden return of Parkinsonian symptoms such as tremors, rigidity, and bradykinesia due to diminished dopaminergic stimulation. By stimulating dopamine receptors in the brain, apomorphine helps alleviate these symptoms, providing rapid relief and improving overall motor function.
The oral suspension form of apomorphine offers several advantages, especially for patients who may have difficulty with subcutaneous injections or prefer an oral route of administration. The liquid form allows for individualized dosing adjustments, catering to specific patient needs and potentially enhancing therapeutic outcomes. It also facilitates ease of swallowing for patients who have dysphagia or other swallowing difficulties common in advanced Parkinson's disease.
For prescribers, this formulation provides flexibility in dosing regimens and can be an essential part of a comprehensive treatment plan for managing Parkinson's disease symptoms. It is crucial to monitor patients for potential side effects, which may include nausea, vomiting, hypotension, and drowsiness. Initiation of therapy may require antiemetic prophylaxis to mitigate gastrointestinal side effects. Regular follow-ups and dose adjustments may be necessary to optimize therapy and minimize adverse effects.
Patients prescribed Apomorphine 30 mg/mL Oral Suspension should use the medication as directed by their healthcare provider. It is important to measure doses accurately using a proper dosing device to ensure efficacy and reduce the risk of side effects. Patients should be advised to report any adverse reactions or concerns promptly to their healthcare team.
This compounded medication is prepared with care by our team of pharmacists at Bayview Pharmacy, adhering to strict compounding standards to ensure the highest quality and safety of the product. Compounded medications like this oral suspension provide personalized treatment options when commercially available medications do not meet patient-specific needs.
If you have any questions about Apomorphine 30 mg/mL Oral Suspension or how it may benefit you or your patients, please reach out to us. Our knowledgeable pharmacists are here to provide assistance and support for all your compounding needs.
Apomorphine 30 mg/mL Oral Suspension is a liquid dosage form designed to provide a homogeneous mixture for administration, ensuring consistent dosing and absorption. This formulation is primarily used in the management of Parkinson's disease, particularly for the treatment of "off" episodes in patients who experience motor fluctuations despite optimized therapy with levodopa/carbidopa. Apomorphine acts as a dopamine agonist, stimulating dopamine receptors in the brain to improve motor control and reduce symptoms such as tremors, stiffness, and slowness of movement.
When considering the use of Apomorphine 30 mg/mL Oral Suspension, it is crucial to be aware of potential drug interactions that may affect its efficacy or increase the risk of adverse effects. One significant interaction is with antiemetic medications. Apomorphine can cause nausea and vomiting, and while antiemetics are often prescribed to manage these side effects, certain antiemetics such as ondansetron and other 5-HT3 antagonists should be avoided due to the risk of profound hypotension and loss of consciousness. Instead, trimethobenzamide is commonly recommended as a safer alternative for managing nausea associated with apomorphine.
Patients taking medications that affect blood pressure should be closely monitored, as apomorphine can cause orthostatic hypotension. This is particularly important for patients on antihypertensive drugs, as the combination may lead to an increased risk of dizziness, fainting, or falls. Adjustments to antihypertensive therapy may be necessary to maintain stable blood pressure levels.
Concomitant use of apomorphine with other central nervous system depressants, such as benzodiazepines, opioids, or alcohol, can enhance sedative effects and increase the risk of respiratory depression. Patients should be advised to avoid or limit the use of these substances while taking apomorphine, and prescribers should consider alternative therapies if necessary.
Apomorphine may also interact with medications that prolong the QT interval, such as certain antipsychotics, antiarrhythmics, and antibiotics. This interaction can increase the risk of cardiac arrhythmias, and caution is advised when prescribing apomorphine to patients taking these medications. Regular monitoring of cardiac function and electrolyte levels may be warranted in such cases.
Additionally, apomorphine's efficacy can be influenced by other dopaminergic agents. Patients receiving other dopamine agonists or levodopa may experience additive effects, which could necessitate dosage adjustments to avoid excessive dopaminergic stimulation and associated side effects, such as dyskinesias or hallucinations.
It is essential for both patients and prescribers to be aware of these potential interactions to optimize treatment outcomes and minimize risks. If you have any questions or concerns regarding the use of Apomorphine 30 mg/mL Oral Suspension and its interactions with other medications, please reach out to us at Bayview Pharmacy for further guidance and support.
This formulation is particularly beneficial for patients who require precise dosing and rapid onset of action, as it allows for the active ingredient to be uniformly dispersed throughout the liquid medium, ensuring consistent delivery with each dose. The oral suspension form is advantageous for patients who may have difficulty swallowing tablets or capsules, providing an easier administration route while maintaining the therapeutic efficacy of the medication.
Apomorphine works primarily by stimulating dopamine receptors in the brain, specifically targeting the D1 and D2 receptor subtypes. This action is crucial in the management of Parkinson's disease, a neurodegenerative disorder characterized by the depletion of dopamine in the brain. By activating these receptors, apomorphine helps to restore the balance of dopamine, thereby alleviating symptoms such as bradykinesia (slowness of movement), rigidity, and tremors. The rapid onset of action of apomorphine makes it particularly useful for managing "off" episodes in Parkinson's disease, where patients experience a sudden return of symptoms due to the waning effects of their regular dopaminergic medications.
In addition to its use in Parkinson's disease, apomorphine has been explored for its potential benefits in treating other conditions characterized by dopaminergic dysfunction. These may include certain types of dystonia and erectile dysfunction, where its ability to modulate dopaminergic pathways can provide therapeutic benefits. However, the primary indication remains the management of motor fluctuations in Parkinson's disease.
The formulation of apomorphine as an oral suspension allows for flexible dosing, which can be tailored to the individual needs of the patient. This is particularly important in managing a condition like Parkinson's disease, where the severity and timing of symptoms can vary significantly between patients. The liquid form also facilitates dose adjustments, which can be made more easily compared to solid dosage forms, allowing for a more personalized approach to treatment.
For prescribers, it is important to consider the pharmacokinetic profile of apomorphine when determining the appropriate dosing regimen. The oral suspension provides a rapid absorption profile, which is beneficial for acute symptom management. However, it is also associated with a relatively short half-life, necessitating multiple doses throughout the day to maintain therapeutic levels. Patients should be monitored for potential side effects, which may include nausea, hypotension, and dyskinesias, and appropriate measures should be taken to mitigate these effects, such as the co-administration of antiemetics.
Patients using apomorphine 30 mg/mL Oral Suspension should be educated on the proper administration technique to ensure accurate dosing. It is crucial to shake the bottle well before each use to ensure the medication is evenly distributed. Patients should also be advised on the importance of adhering to their prescribed dosing schedule and to report any adverse effects or concerns to their healthcare provider promptly.
If you have any questions or require further information about apomorphine 30 mg/mL Oral Suspension, please do not hesitate to reach out to us at Bayview Pharmacy. Our team of compounding pharmacists is here to assist you with any inquiries you may have regarding this formulation and its use in treating disease states.
Apomorphine 30 mg/mL Oral Suspension is primarily used to treat episodes of immobility in patients with Parkinson's disease.
Apomorphine Oral Suspension should be taken as directed by your healthcare provider. It is important to measure the dose accurately using a proper measuring device and to follow the prescribed schedule for administration.
Apomorphine Oral Suspension can be taken with or without food. However, it is important to follow your healthcare provider's instructions regarding food intake, as it may affect the absorption or effectiveness of the medication.
If you miss a dose of Apomorphine Oral Suspension, take it as soon as you remember. If it is almost time for your next dose, skip the missed dose and continue with your regular dosing schedule. Do not double the dose to catch up.
Common side effects of Apomorphine Oral Suspension may include nausea, vomiting, dizziness, and drowsiness. If you experience severe side effects or allergic reactions, contact your healthcare provider immediately.
Store Apomorphine Oral Suspension at room temperature, away from light and moisture. Keep it out of reach of children and pets. Do not freeze the suspension.
Apomorphine may cause dizziness or drowsiness. It is advised to avoid driving or operating heavy machinery until you know how the medication affects you. Consult your healthcare provider for specific guidance.
The safety of Apomorphine Oral Suspension during pregnancy or breastfeeding is not well established. Consult your healthcare provider to discuss potential risks and benefits before using this medication if you are pregnant or breastfeeding.
Yes, Apomorphine Oral Suspension can interact with other medications, including certain antidepressants, antihypertensives, and antiemetics. Inform your healthcare provider about all the medications you are taking to avoid potential interactions.
In case of an overdose, seek immediate medical attention or contact a poison control center. Symptoms of overdose may include severe nausea, vomiting, dizziness, or fainting.
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.
Take orally