Isoniazid 5 mg/mL Oral Suspension is a liquid dosage form in which isoniazid is uniformly dispersed throughout a liquid medium, ensuring a homogeneous mixture for administration. This formulation is primarily used in the treatment of tuberculosis.

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.
This compounded suspension provides a homogeneous mixture, ensuring uniform dosing for patients who may have difficulty swallowing tablets or require precise dosing adjustments.
As a first-line agent against Mycobacterium tuberculosis, isoniazid works by inhibiting the synthesis of mycolic acids, which are essential components of the bacterial cell wall. This action leads to the eventual death of the bacteria, making it a critical medication in both active TB treatment regimens and latent TB infection prophylaxis.
The oral suspension form is particularly beneficial for pediatric patients, elderly patients, or those with swallowing difficulties, as it allows for easier administration and more accurate dose adjustments based on body weight and specific medical needs. The 5 mg/mL concentration facilitates precise dosing, which is essential for maximizing therapeutic effectiveness while minimizing the risk of adverse effects.
For prescribers, it's important to consider that isoniazid therapy may require supplementation with pyridoxine (vitamin B6) to prevent peripheral neuropathy, a known side effect of isoniazid. Monitoring liver function tests is also recommended, as hepatotoxicity is a potential risk, especially in patients with pre-existing liver conditions or those consuming alcohol regularly.
Patients should be counseled on the importance of adhering to the dosing schedule to prevent the development of drug-resistant TB strains. They should also be made aware of potential side effects, such as fatigue, numbness, or tingling in extremities, and advised to report any unusual symptoms to their healthcare provider promptly.
The suspension should be stored in a tightly closed container, away from light and at room temperature, unless otherwise instructed. Shake well before each use to ensure proper distribution of the medication throughout the liquid.
If you have any questions, reach out to us.
Isoniazid 5 mg/mL Oral Suspension is a liquid dosage form designed to provide a homogeneous mixture for administration, ensuring that the active ingredient is uniformly dispersed throughout the liquid medium. This formulation is primarily used in the treatment of tuberculosis and other mycobacterial infections. However, it is crucial for both patients and prescribers to be aware of potential drug interactions that may affect the efficacy and safety of isoniazid therapy.
Isoniazid is known to interact with a variety of medications, which can lead to either increased toxicity or reduced therapeutic effects. One of the most significant interactions is with rifampin, another antitubercular agent. When used concurrently, isoniazid and rifampin can increase the risk of hepatotoxicity. Therefore, liver function should be monitored closely, and patients should be advised to report any symptoms of liver dysfunction, such as jaundice, fatigue, or abdominal pain.
Another important interaction is with phenytoin, an anticonvulsant used to treat seizures. Isoniazid can inhibit the metabolism of phenytoin, leading to increased plasma levels and potential toxicity. Patients on concurrent therapy should have their phenytoin levels monitored, and dose adjustments may be necessary to avoid adverse effects such as nystagmus, ataxia, or confusion.
Isoniazid can also interact with certain antidepressants, particularly selective serotonin reuptake inhibitors (SSRIs) and monoamine oxidase inhibitors (MAOIs). These interactions can lead to increased side effects or reduced efficacy of the antidepressants. It is important for prescribers to evaluate the risk-benefit ratio of concurrent use and consider alternative therapies if necessary.
Additionally, isoniazid may affect the metabolism of certain benzodiazepines, such as diazepam, leading to increased sedation and respiratory depression. Patients should be monitored for signs of excessive sedation, and dose adjustments of the benzodiazepine may be required.
Alcohol consumption should be minimized or avoided during isoniazid therapy, as it can exacerbate the risk of liver damage. Patients should be counseled on the importance of adhering to this recommendation to prevent potential hepatotoxicity.
For patients taking antacids, it is advisable to separate the administration of isoniazid and antacids by at least two hours, as antacids can interfere with the absorption of isoniazid, reducing its effectiveness.
It is essential for healthcare providers to review a patient's complete medication profile, including over-the-counter drugs and supplements, to identify any potential interactions with isoniazid. Patients should be encouraged to communicate openly about all medications they are taking to ensure appropriate treatment.
If you have any questions or need further information regarding the use of Isoniazid 5 mg/mL Oral Suspension and its potential drug interactions, please reach out to us at Bayview Pharmacy. Our team of knowledgeable compounding pharmacists is here to assist you.
Isoniazid 5 mg/mL Oral Suspension is a liquid dosage form designed to deliver the active pharmaceutical ingredient, isoniazid, in a homogeneous mixture. This formulation ensures that each milliliter of the suspension contains an exact concentration of 5 mg of isoniazid, providing consistent dosing for patients. The liquid medium allows for the uniform dispersion of isoniazid, making it easier to administer, especially for patients who may have difficulty swallowing tablets or capsules. This is particularly beneficial for pediatric patients or those with swallowing difficulties, ensuring they receive the correct dose without the challenges associated with solid dosage forms.
Isoniazid is an antibiotic that is primarily used in the treatment and prevention of tuberculosis (TB). It works by inhibiting the synthesis of mycolic acids, which are essential components of the mycobacterial cell wall. By disrupting the production of these acids, isoniazid effectively weakens and kills the bacteria responsible for tuberculosis. This mechanism of action makes isoniazid a critical component in the treatment regimen for TB, often used in combination with other antitubercular drugs to prevent the development of drug-resistant strains of the bacteria.
The oral suspension form of isoniazid provides several advantages in the treatment of tuberculosis. The liquid form allows for flexible dosing, which can be easily adjusted based on the patient's age, weight, and specific medical needs. This is particularly important in pediatric cases, where precise dosing is crucial for both efficacy and safety. Additionally, the suspension form can improve patient adherence to the treatment regimen, as it is often more palatable and easier to ingest than solid forms.
It is important to monitor patients for potential side effects, such as liver toxicity, and to ensure that they adhere to the prescribed treatment plan to achieve the best possible outcomes. Regular follow-up and patient education are essential components of successful tuberculosis management.
If you have any questions about this formulation or its use in treating tuberculosis, 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.
Isoniazid 5 mg/mL Oral Suspension is a liquid dosage form where the active ingredient, Isoniazid, is uniformly dispersed in a liquid medium, creating a homogeneous mixture for easy administration.
This oral suspension is primarily used for the treatment and prevention of tuberculosis (TB) by inhibiting the growth of the bacteria that cause the disease.
Store the suspension at room temperature, away from direct sunlight and moisture. Ensure the bottle is tightly closed when not in use to maintain its stability and effectiveness.
The suspension should be administered orally, using a proper measuring device to ensure accurate dosing. It is important to follow the healthcare provider's instructions regarding dosage and frequency.
It is generally recommended to take Isoniazid on an empty stomach, either 1 hour before or 2 hours after meals, to enhance absorption. However, if stomach upset occurs, it can be taken with food.
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, and mild skin rash. Serious side effects can include liver problems and peripheral neuropathy. Contact your healthcare provider if you experience any severe or persistent symptoms.
Yes, Isoniazid can interact with certain medications, including antacids, acetaminophen, and some anticonvulsants. It is important to inform your healthcare provider of all medications and supplements you are taking.
Isoniazid can be prescribed to children for the treatment and prevention of tuberculosis. The dosage will be determined by the healthcare provider based on the child's weight and medical condition.
Regular monitoring of liver function is recommended during treatment. Avoid alcohol consumption, as it can increase the risk of liver damage. Inform your healthcare provider of any existing medical conditions, especially liver disease or a history of alcoholism.
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