Desmopressin Acetate 0.033 mg/ml Oral Suspension is a compounded medication, uniformly dispersed in a liquid medium for easy administration. It is used in the treatment of conditions such as Nephrogenic Diabetes Insipidus, Primary Nocturnal Enuresis, Central Diabetes Insipidus, Von Willebrand Disease, and Hemophilia A.

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.
Desmopressin Acetate 0.033 mg/ml Oral Suspension is a compounded medication designed to treat a range of conditions, including diabetes insipidus, nocturnal enuresis, and von Willebrand disease. This medication functions by augmenting the quantity of antidiuretic hormone in the body, which aids in reducing urine production and enhancing water absorption in the kidneys. The formulation is available in an oral suspension form, a liquid dosage form where one or more ingredients are uniformly dispersed throughout a liquid medium, creating a homogeneous mixture for administration. This form is easy to consume and can be taken with or without food.
For patients suffering from diabetes insipidus, Desmopressin Acetate 0.033 mg/ml Oral Suspension can help manage the condition by reducing the volume of urine produced and increasing the absorption of water in the kidneys. This can alleviate symptoms such as excessive thirst and frequent urination.
In the case of nocturnal enuresis, Desmopressin Acetate 0.033 mg/ml Oral Suspension can help decrease the volume of urine produced during the night, thereby reducing the frequency of bedwetting incidents.
For patients with von Willebrand disease, Desmopressin Acetate 0.033 mg/ml Oral Suspension can aid in increasing the amount of clotting factor VIII in the body, which can help mitigate the risk of bleeding.
If you have any queries about this formulation or how it can assist in treating your condition, please do not hesitate to contact us at Bayview Pharmacy. We are here to provide you with the necessary information and support.
Desmopressin Acetate 0.033 mg/ml Oral Suspension is a compounded formulation designed for the treatment of central diabetes insipidus, primary nocturnal enuresis, and the management of increased thirst and/or urination associated with certain types of head trauma or surgery involving the pituitary gland. This medication should be taken as directed by your healthcare provider, and it is crucial to adhere to the prescribed dosage without deviation.
It's important to note that Desmopressin Acetate 0.033 mg/ml Oral Suspension may interact with other medications, including diuretics, lithium, and nonsteroidal anti-inflammatory drugs (NSAIDs). Therefore, it is essential to inform your healthcare provider about all medications, vitamins, and herbal supplements you are currently taking.
Some potential side effects of Desmopressin Acetate 0.033 mg/ml Oral Suspension include dizziness, drowsiness, or blurred vision. It is advised not to drive or operate heavy machinery until you understand how this medication affects you. Additionally, this medication may cause dehydration, so ensure to drink plenty of fluids while taking it.
Desmopressin Acetate 0.033 mg/ml Oral Suspension may cause an increase in blood pressure, sodium, potassium, calcium, magnesium, uric acid, and creatinine levels in the blood. Regular monitoring of these levels is recommended while taking this medication. If you have any questions about the interactions of Desmopressin Acetate 0.033 mg/ml Oral Suspension, please consult with your healthcare provider.
Desmopressin Acetate 0.033 mg/ml Oral Suspension is a compounded medication that is used to manage a variety of health conditions. This includes central diabetes insipidus, nocturnal enuresis, also known as bedwetting, and von Willebrand disease. The medication functions by increasing the levels of antidiuretic hormone (ADH) in the body, which aids in water retention and reduces urine production.
For the management of central diabetes insipidus, Desmopressin Acetate 0.033 mg/ml Oral Suspension is typically administered orally once or twice daily. The specific dosage and frequency of administration are determined based on the individual patient's response to the medication.
In the case of nocturnal enuresis, Desmopressin Acetate 0.033 mg/ml Oral Suspension is usually taken orally once daily, typically at bedtime. Again, the exact dosage and frequency of administration are tailored to the individual patient's response to the medication.
For patients with von Willebrand disease, Desmopressin Acetate 0.033 mg/ml Oral Suspension is generally taken orally once or twice daily. The dosage and frequency of administration are adjusted based on the individual patient's response to the medication.
Desmopressin Acetate 0.033 mg/ml Oral Suspension is generally well tolerated by most patients. However, some may experience side effects such as headache, nausea, vomiting, abdominal pain, and dizziness. If any of these side effects occur, it is recommended that patients contact their healthcare provider immediately.
If you have any questions about Desmopressin Acetate 0.033 mg/ml Oral Suspension or its use in treating these health conditions, please do not hesitate to reach out for more information.
Desmopressin Acetate 0.033 mg/ml Oral Suspension is a liquid medication that contains the active ingredient Desmopressin Acetate. It is a homogeneous mixture where the active ingredient is uniformly dispersed throughout a liquid medium.
This medication is taken orally. The exact dosage and frequency will be determined by your healthcare provider based on your specific condition and response to treatment.
Desmopressin Acetate is used to control the amount of urine your kidneys make. It is often used to treat conditions like diabetes insipidus and certain kinds of head injury or surgery. It can also be used to manage bedwetting problems.
Some common side effects include headache, nausea, upset stomach, or flushing of the face. If any of these effects persist or worsen, notify your doctor or pharmacist promptly.
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. Take your next dose at the regular time. Do not double the dose to catch up.
Before starting this medication, inform your doctor about all the products you use, including prescription drugs, nonprescription drugs, and herbal products. Some products may interact with Desmopressin Acetate, affecting how it works.
Store at room temperature away from light and moisture. Do not store in the bathroom. Keep all medications away from children and pets.
If someone has overdosed and has serious symptoms such as passing out or trouble breathing, call emergency services immediately. Symptoms of overdose may include confusion, drowsiness, persistent/severe headache, sudden weight gain, or seizures.
Consult your doctor before using this medication if you are pregnant, planning to become pregnant, or are breastfeeding. The risks and benefits will be discussed with your healthcare provider.
If you have an allergic reaction, such as rash, itching/swelling (especially of the face/tongue/throat), severe dizziness, or trouble breathing, seek immediate medical attention.
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