Prochlorperazine 5 mg/0.1mL Nasal Spray is a liquid formulation delivered in a spray form, specifically designed for administration into the nasal cavity. This formulation provides targeted local or systemic effects through the nostrils.
It is used to treat nausea, vomiting, and vertigo associated with various conditions, including migraines and vestibular disorders. The nasal spray allows for rapid absorption and onset of action.

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.
Prochlorperazine 5 mg/0.1mL Nasal Spray is a specially compounded medication designed to manage symptoms of severe nausea and vomiting. Prochlorperazine is a phenothiazine derivative that works by blocking dopamine receptors in the brain, particularly in the chemoreceptor trigger zone, thus preventing the initiation of the vomiting reflex. By formulating it as a nasal spray, the medication offers rapid absorption through the rich vascular network of the nasal mucosa, resulting in a quicker onset of action compared to traditional oral tablets or suppositories.
Prochlorperazine 5 mg/0.1mL Nasal Spray is a formulation designed for intranasal administration, providing both local and systemic effects. It is primarily used to treat conditions such as nausea, vomiting, and vertigo, and may also be used in the management of migraine headaches. As with any medication, it is important to be aware of potential drug interactions that could affect the efficacy and safety of this treatment.
Prochlorperazine is a phenothiazine derivative, which functions as a dopamine receptor antagonist. It is important to consider its interactions with other medications that may also affect dopamine pathways or have central nervous system effects. Patients and prescribers should be particularly cautious when using this nasal spray in conjunction with other central nervous system depressants, such as benzodiazepines, opioids, or alcohol, as these combinations can enhance sedative effects and potentially lead to respiratory depression or profound sedation.
Additionally, prochlorperazine may interact with medications that prolong the QT interval, such as certain antiarrhythmics, antipsychotics, and antibiotics. This interaction can increase the risk of serious cardiac arrhythmias, including torsades de pointes. It is advisable to monitor cardiac function and consider alternative treatments if the patient is already on medications known to affect the QT interval.
Patients taking antihypertensive medications should be aware that prochlorperazine can potentiate the hypotensive effects of these drugs, leading to an increased risk of dizziness, lightheadedness, or fainting. It is important to monitor blood pressure regularly and adjust antihypertensive therapy as needed.
Prochlorperazine may also interact with anticholinergic medications, such as those used to treat Parkinson's disease, irritable bowel syndrome, or overactive bladder. The combination can exacerbate anticholinergic side effects, including dry mouth, constipation, urinary retention, and confusion, particularly in elderly patients.
Patients on anticoagulant therapy, such as warfarin, should be monitored closely, as prochlorperazine may alter the metabolism of these drugs, potentially affecting their anticoagulant effects. Regular monitoring of INR levels is recommended to ensure therapeutic efficacy and safety.
It is crucial for patients and prescribers to maintain open communication regarding all medications being taken, including over-the-counter drugs and supplements, to avoid potential interactions. If you have any questions or concerns about drug interactions with Prochlorperazine 5 mg/0.1mL Nasal Spray, please reach out to us at Bayview Pharmacy for further guidance and support.
Prochlorperazine 5 mg/0.1mL Nasal Spray is a specialized liquid formulation designed for intranasal administration, offering a unique and effective method for delivering medication directly through the nasal cavity. This delivery system is particularly advantageous for achieving both local and systemic therapeutic effects. The nasal cavity is highly vascularized, which allows for rapid absorption of the medication into the bloodstream, bypassing the gastrointestinal tract and first-pass metabolism in the liver. This can result in faster onset of action and improved bioavailability compared to oral administration.
Prochlorperazine is an antipsychotic and antiemetic medication that works primarily by blocking dopamine receptors in the brain. By inhibiting these receptors, prochlorperazine can effectively manage symptoms associated with nausea, vomiting, and certain psychiatric disorders. The nasal spray formulation is particularly beneficial for patients who may have difficulty swallowing pills or who require rapid relief from symptoms. Additionally, the nasal route can be advantageous for patients experiencing nausea and vomiting, as it avoids the gastrointestinal tract where absorption might be compromised.
For prescribers, the nasal spray formulation of prochlorperazine offers a versatile option for treating a variety of conditions. It can be used in the management of acute migraine attacks, where nausea and vomiting are common symptoms, as well as in the treatment of vertigo and other conditions where rapid symptom control is desired. The precise dosing of 5 mg/0.1mL allows for accurate titration and control over the therapeutic effects, minimizing the risk of side effects associated with higher systemic concentrations of the drug.
Patients using Prochlorperazine 5 mg/0.1mL Nasal Spray should be instructed on the proper technique for administration to ensure optimal absorption and efficacy. It is important to gently insert the spray nozzle into the nostril and administer the prescribed dose while inhaling gently. This helps to ensure that the medication is distributed evenly across the nasal mucosa, facilitating absorption. Patients should also be advised to avoid blowing their nose immediately after administration to allow sufficient time for the medication to be absorbed.
If you have any questions about Prochlorperazine 5 mg/0.1mL Nasal Spray, its use, or its administration, please do not hesitate to 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 regarding this formulation.
Prochlorperazine 5 mg/0.1mL Nasal Spray is used to treat nausea and vomiting, and it may also be used for other conditions as determined by your healthcare provider. It is delivered through the nasal cavity for targeted local or systemic effects.
The nasal spray formulation allows the medication to be absorbed through the nasal mucosa, providing rapid onset of action and potentially reducing systemic side effects compared to oral administration.
To use the nasal spray, insert the nozzle into one nostril, close the other nostril with a finger, and spray the prescribed dose while inhaling gently. Follow your healthcare provider's instructions for the correct dosage and frequency.
Common side effects may include nasal irritation, dizziness, drowsiness, or headache. If you experience severe side effects or signs of an allergic reaction, seek medical attention immediately.
If you are pregnant or breastfeeding, consult your healthcare provider before using Prochlorperazine Nasal Spray to discuss potential risks and benefits.
Store the nasal spray at room temperature, away from direct sunlight and moisture. Keep it out of reach of children and pets.
If you miss a dose, use it as soon as you remember. If it is almost time for your next dose, skip the missed dose and resume your regular dosing schedule. Do not double the dose to catch up.
Before using other nasal sprays, consult your healthcare provider to ensure there are no interactions or contraindications with Prochlorperazine Nasal Spray.
The suitability of Prochlorperazine Nasal Spray for children depends on the specific case and should be determined by a healthcare provider. Always follow the guidance of a healthcare professional for pediatric use.
If you experience severe side effects such as difficulty breathing, swelling, or severe dizziness, seek immediate medical attention. Contact your healthcare provider for guidance on managing any adverse effects.
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.
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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.
Inhale intranasally