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Nitrofurantoin 2 mg/mL Oral Suspension is a liquid dosage form where nitrofurantoin is uniformly dispersed in a liquid medium, ensuring a homogeneous mixture for administration.
This formulation is primarily used to treat urinary tract infections (UTIs).
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.
Nitrofurantoin 2 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 to treat urinary tract infections (UTIs) caused by susceptible strains of bacteria. Nitrofurantoin works by interfering with bacterial cell wall synthesis, ultimately leading to the death of the bacteria.
When considering the use of Nitrofurantoin 2 mg/mL Oral Suspension, it is crucial to be aware of potential drug interactions that may affect the efficacy and safety of the treatment. One significant interaction is with antacids containing magnesium trisilicate, which can reduce the absorption of nitrofurantoin, leading to decreased effectiveness. Patients should be advised to avoid taking such antacids concurrently with this medication.
Another important interaction is with probenecid and sulfinpyrazone, which are medications used to treat gout. These drugs can inhibit the renal tubular secretion of nitrofurantoin, resulting in increased blood levels and potential toxicity. Therefore, concurrent use should be avoided or closely monitored by healthcare professionals.
Additionally, nitrofurantoin may interact with certain antibiotics, such as quinolones, potentially reducing their antibacterial efficacy. It is advisable to avoid using nitrofurantoin in combination with quinolones unless absolutely necessary and under the guidance of a healthcare provider.
Patients with renal impairment should use nitrofurantoin with caution, as reduced kidney function can lead to accumulation of the drug and increased risk of adverse effects. It is essential for prescribers to assess renal function before initiating treatment and adjust the dosage accordingly.
For patients taking oral contraceptives, it is important to note that while nitrofurantoin is not known to significantly reduce the effectiveness of birth control pills, it is always prudent to use additional contraceptive methods as a precautionary measure during antibiotic treatment.
Healthcare providers should also be aware of the potential for nitrofurantoin to cause pulmonary reactions, particularly in patients with pre-existing lung conditions. Monitoring for respiratory symptoms is recommended, and any new or worsening symptoms should be promptly evaluated.
As with any medication, it is essential for both patients and prescribers to be vigilant about potential interactions and side effects. If you have any questions or concerns regarding the use of Nitrofurantoin 2 mg/mL Oral Suspension, please reach out to us for further information and guidance.
Nitrofurantoin 2 mg/mL Oral Suspension is a liquid dosage form designed to deliver the active pharmaceutical ingredient, nitrofurantoin, in a homogeneous mixture. This formulation ensures that the medication is evenly dispersed throughout the liquid medium, allowing for precise dosing and ease of administration, particularly for patients who may have difficulty swallowing tablets or capsules. The suspension is carefully compounded to maintain stability and efficacy, ensuring that each milliliter contains an accurate dose of 2 mg of nitrofurantoin.
Nitrofurantoin is an antibiotic that is primarily used to treat urinary tract infections (UTIs) caused by susceptible strains of bacteria. It works by interfering with the bacterial cell wall synthesis and protein synthesis, ultimately leading to the death of the bacteria. The oral suspension form allows for rapid absorption in the gastrointestinal tract, leading to effective concentrations in the urinary tract where the infection is located.
For prescribers, the nitrofurantoin 2 mg/mL oral suspension offers a flexible dosing option, particularly useful for pediatric patients or those requiring dose adjustments based on renal function or other clinical considerations. The liquid form allows for easy titration of doses, ensuring that patients receive the appropriate amount of medication tailored to their specific needs. Additionally, the suspension can be flavored to improve palatability, enhancing patient compliance, especially in children.
The liquid form is easy to swallow and can be measured accurately using a dosing syringe or cup, ensuring that the correct dose is administered each time. Patients should be advised to shake the bottle well before each use to ensure the medication is evenly distributed throughout the suspension. It is also important to complete the full course of therapy as prescribed, even if symptoms improve, to ensure the infection is fully eradicated and to prevent the development of antibiotic resistance.
If you have any questions about this formulation or its use, 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 to ensure the safe and appropriate use of nitrofurantoin 2 mg/mL oral suspension.
Nitrofurantoin 2 mg/mL Oral Suspension is a liquid dosage form of the antibiotic nitrofurantoin, where the active ingredient is uniformly dispersed in a liquid medium to create a homogeneous mixture for easy administration.
This oral suspension is used to treat urinary tract infections caused by certain bacteria. It works by stopping the growth of bacteria.
Store the suspension at room temperature, away from light and moisture. Do not freeze. Keep it out of reach of children and pets.
Shake the bottle well before each use. Measure the prescribed dose using a special measuring device or spoon. Do not use a household spoon to avoid incorrect dosing.
Yes, it is recommended to take this medication with food to enhance absorption and reduce stomach upset.
If you miss a dose, take it as soon as you remember. If it is near the time of the next dose, skip the missed dose and resume your usual dosing schedule. Do not double the dose to catch up.
Common side effects may include nausea, headache, and diarrhea. If you experience severe side effects such as persistent cough, chest pain, or signs of an allergic reaction, seek medical attention immediately.
Yes, but the dosage and duration of treatment should be determined by a healthcare professional based on the child's age, weight, and medical condition.
Consult your healthcare provider before using this medication during pregnancy. It should only be used if clearly needed and prescribed by a healthcare professional.
It is advisable to avoid alcohol while taking this medication, as it may increase the risk of side effects and reduce the effectiveness of the treatment.
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.
Search by NCPDP 4106882, or by name and ZIP: Bayview Pharmacy, Warwick, RI 02886. Select it as the destination pharmacy and save it as a favorite. Click any value to copy it.
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
