Propranolol Hydrochloride 10 mg/mL Oral Suspension is a liquid dosage form in which propranolol hydrochloride is dispersed uniformly throughout a liquid medium, ensuring a homogeneous mixture for administration. This formulation is primarily used to manage hypertension, angina pectoris, and certain types of arrhythmias. The oral suspension allows for precise dosing and is suitable for patients who may have difficulty swallowing tablets.

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.
Propranolol Hydrochloride 10 mg/mL Oral Suspension is a medication formulated as a liquid dosage form, where propranolol hydrochloride is uniformly dispersed throughout a liquid medium to create a homogeneous mixture for administration. This oral suspension is particularly beneficial for patients who have difficulty swallowing tablets or capsules, such as children or the elderly, and allows for precise dosing adjustments to meet individual patient needs.
Propranolol is a non-selective beta-adrenergic receptor blocker that works by inhibiting the action of catecholamines (epinephrine and norepinephrine) on both beta-1 and beta-2 adrenergic receptors. This action results in decreased heart rate, reduced cardiac output, and lowered blood pressure. It is commonly prescribed for hypertension (high blood pressure), angina pectoris (chest pain), arrhythmias (irregular heartbeats), and prevention of myocardial infarction (heart attack).
In addition to cardiovascular applications, propranolol is used in the treatment of other conditions such as migraine prophylaxis, essential tremor, and certain types of anxiety, including performance anxiety. Its ability to cross the blood-brain barrier allows it to have central nervous system effects, which can be beneficial in these clinical scenarios. The 10 mg/mL oral suspension provides flexibility in dosing, allowing for gradual titration and optimization of therapeutic effects while minimizing side effects.
Patients prescribed this medication should be aware of potential side effects, which may include dizziness, fatigue, gastrointestinal disturbances, and cold extremities due to decreased circulation. It is important to take propranolol exactly as directed by a healthcare provider and not to discontinue use abruptly, as this may lead to adverse cardiovascular events such as rebound hypertension or exacerbation of angina symptoms.
Healthcare providers should consider the patient's overall medical condition before prescribing propranolol, especially in those with respiratory conditions like asthma or chronic obstructive pulmonary disease (COPD), as beta-blockers can induce bronchoconstriction. Caution is also advised in patients with diabetes mellitus, as propranolol may mask signs of hypoglycemia. Regular monitoring of blood pressure, heart rate, and clinical response is recommended to ensure safe and appropriate use of this medication.
If you have any questions, reach out to us.
Propranolol Hydrochloride 10 mg/mL Oral Suspension is a liquid dosage form designed to provide a homogeneous mixture for administration, ensuring consistent dosing and ease of use, particularly for patients who may have difficulty swallowing tablets. This formulation is commonly used in the management of various cardiovascular conditions, including hypertension, angina pectoris, and arrhythmias, as well as in the treatment of anxiety and migraine prophylaxis. However, it is crucial to be aware of potential drug interactions that may affect the efficacy and safety of propranolol when used in combination with other medications.
Propranolol is a non-selective beta-adrenergic receptor blocker, and its interaction profile is influenced by its mechanism of action. Concomitant use of propranolol with other antihypertensive agents, such as calcium channel blockers (e.g., verapamil, diltiazem), can lead to additive effects, potentially resulting in excessive hypotension or bradycardia. Patients should be monitored closely for signs of low blood pressure and slow heart rate, and dose adjustments may be necessary.
Co-administration with antiarrhythmic drugs, such as amiodarone or quinidine, can also enhance the effects of propranolol, increasing the risk of bradycardia, heart block, or other cardiac conduction abnormalities. It is important for prescribers to evaluate the risk-benefit ratio and consider alternative therapies or adjust dosages accordingly.
Propranolol may interact with medications that affect hepatic enzyme activity, such as CYP2D6 inhibitors (e.g., fluoxetine, paroxetine) or inducers (e.g., rifampin, phenytoin). Inhibitors can increase propranolol plasma concentrations, heightening the risk of adverse effects, while inducers may decrease its effectiveness. Regular monitoring and possible dose adjustments are recommended when these drugs are used concurrently.
Non-steroidal anti-inflammatory drugs (NSAIDs), such as ibuprofen or naproxen, may reduce the antihypertensive effects of propranolol. Patients should be advised to use these medications cautiously and under medical supervision, especially if they are being treated for hypertension.
Additionally, propranolol can potentiate the hypoglycemic effects of insulin and oral antidiabetic drugs, masking symptoms of hypoglycemia such as tachycardia. Diabetic patients should be counseled on recognizing other signs of low blood sugar and may require more frequent blood glucose monitoring.
Alcohol consumption can enhance the hypotensive effects of propranolol, leading to dizziness or fainting. Patients should be advised to limit alcohol intake and be cautious when standing up quickly from a sitting or lying position.
For both patients and prescribers, it is essential to maintain open communication regarding all medications being taken, including over-the-counter drugs and supplements, to manage potential interactions effectively. If you have any questions or concerns about drug interactions with Propranolol Hydrochloride 10 mg/mL Oral Suspension, please reach out to us for further guidance and support.
Propranolol Hydrochloride 10 mg/mL Oral Suspension is a liquid dosage form designed to deliver the active ingredient, propranolol hydrochloride, in a uniform and easily administrable manner. This formulation is particularly beneficial for patients who have difficulty swallowing tablets or require precise dosing adjustments, such as pediatric or geriatric patients. The suspension ensures that the propranolol is evenly distributed throughout the liquid medium, allowing for consistent dosing with each administration.
Propranolol is a non-selective beta-adrenergic receptor blocker, commonly known as a beta-blocker. It works by inhibiting the action of certain natural chemicals in the body, such as epinephrine, on the heart and blood vessels. This action results in a decrease in heart rate, blood pressure, and strain on the heart. By blocking beta-adrenergic receptors, propranolol reduces the heart's workload and helps it to beat more regularly, which is particularly useful in treating conditions such as hypertension, angina, and certain types of arrhythmias.
In addition to cardiovascular conditions, propranolol is also used to manage other disease states. Propranolol is also used in the treatment of essential tremor, a neurological disorder that causes involuntary and rhythmic shaking. By modulating the nervous system's response, propranolol can help reduce the amplitude of tremors. Furthermore, it is sometimes prescribed for anxiety, particularly performance anxiety, due to its ability to mitigate the physical symptoms associated with stress, such as rapid heartbeat and trembling.
The oral suspension form of propranolol hydrochloride allows for flexible dosing, which can be crucial for titrating the dose to achieve optimal therapeutic effects while minimizing side effects. The liquid form also facilitates administration in patients who may have difficulty with solid dosage forms, ensuring adherence to prescribed treatment regimens. It is important for both patients and prescribers to understand the pharmacokinetics of propranolol, as it is metabolized primarily by the liver and may interact with other medications. Therefore, careful monitoring and dose adjustments may be necessary to achieve the desired therapeutic outcomes.
If you have any questions about Propranolol Hydrochloride 10 mg/mL Oral Suspension or its use in treating specific conditions, please reach out to us at Bayview Pharmacy. Our team of compounding pharmacists is here to provide you with the information and support you need.
Propranolol Hydrochloride Oral Suspension is used to treat high blood pressure, irregular heartbeats, shaking (tremors), and other conditions as determined by your healthcare provider. It works by blocking certain natural chemicals in your body, such as epinephrine, to lower heart rate, blood pressure, and strain on the heart.
Take the oral suspension exactly as prescribed by your healthcare provider. Shake the bottle well before each use to ensure the medication is evenly distributed. Use a proper measuring device to ensure you are taking the correct dose.
Yes, you can take Propranolol Hydrochloride Oral Suspension with or without food. However, it is best to take it the same way each time to maintain consistent blood levels of the medication.
If you miss a dose, take 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.
Common side effects may include nausea, vomiting, diarrhea, stomach cramps, decreased heart rate, and fatigue. If you experience severe side effects such as difficulty breathing, swelling, or severe dizziness, seek medical attention immediately.
Store the oral suspension at room temperature, away from light and moisture. Do not freeze. Keep the bottle tightly closed and out of reach of children and pets.
Propranolol may cause dizziness or fatigue. Avoid driving or operating heavy machinery until you know how the medication affects you. Consult your healthcare provider if you have concerns about these activities.
The safety and effectiveness of Propranolol Hydrochloride Oral Suspension in children depend on the condition being treated and the child's age and weight. Always follow your healthcare provider's instructions regarding pediatric use.
Alcohol can increase the blood pressure-lowering effects of propranolol, which may lead to dizziness or fainting. It is advisable to limit or avoid alcohol consumption while taking this medication.
If you experience symptoms of an allergic reaction, such as rash, itching, swelling, severe dizziness, or difficulty breathing, seek immediate medical attention. Discontinue use and inform your healthcare provider.
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.
Take orally