Diabetes Insipidus (DI) Treatments

Find Diabetes Insipidus (DI) Treatments

Generic Name

Desmopressin Acetate

Brand Names
DDAVP, Desmoda
FDA approval date: May 01, 1984
Classification: Factor VIII Activator
Form: Injection, Spray, Tablet, Solution

What is DDAVP (Desmopressin Acetate)?

Hemophilia A DDAVP Injection 4 mcg/mL is indicated for patients with hemophilia A with factor VIII coagulant activity levels greater than 5%. DDAVP will often maintain hemostasis in patients with hemophilia A during surgical procedures and postoperatively when administered 30 minutes prior to scheduled procedure. DDAVP will also stop bleeding in hemophilia A patients with episodes of spontaneous or trauma-induced injuries such as hemarthroses, intramuscular hematomas or mucosal bleeding. DDAVP is not indicated for the treatment of hemophilia A with factor VIII coagulant activity levels equal to or less than 5%, or for the treatment of hemophilia B, or in patients who have factor VIII antibodies. In certain clinical situations, it may be justified to try DDAVP in patients with factor VIII levels between 2% to 5%; however, these patients should be carefully monitored. von Willebrand's Disease DDAVP Injection 4 mcg/mL is indicated for patients with mild to moderate classic von Willebrand's disease with factor VIII levels greater than 5%. DDAVP will often maintain hemostasis in patients with mild to moderate von Willebrand's disease during surgical procedures and postoperatively when administered 30 minutes prior to the scheduled procedure. DDAVP will usually stop bleeding in mild to moderate von Willebrand's patients with episodes of spontaneous or trauma-induced injuries such as hemarthroses, intramuscular hematomas or mucosal bleeding. Those von Willebrand's disease patients who are least likely to respond are those with severe homozygous von Willebrand's disease with factor VIII coagulant activity and factor VIII von Willebrand factor antigen levels less than 1%. Other patients may respond in a variable fashion depending on the type of molecular defect they have. Bleeding time and factor VIII coagulant activity, ristocetin cofactor activity, and von Willebrand factor antigen should be checked during administration of DDAVP to ensure that adequate levels are being achieved. DDAVP is not indicated for the treatment of severe classic von Willebrand's disease and when there is evidence of an abnormal molecular form of factor VIII antigen. Diabetes Insipidus DDAVP Injection 4 mcg/mL is indicated as antidiuretic replacement therapy in the management of central diabetes insipidus and for the management of the temporary polyuria and polydipsia following head trauma or surgery in the pituitary region. DDAVP is ineffective for the treatment of nephrogenic diabetes insipidus. DDAVP is also available as an intranasal preparation. However, this means of delivery can be compromised by a variety of factors that can make nasal insufflation ineffective or inappropriate. These include poor intranasal absorption, nasal congestion and blockage, nasal discharge, atrophy of nasal mucosa, and severe atrophic rhinitis. Intranasal delivery may be inappropriate where there is an impaired level of consciousness. In addition, cranial surgical procedures, such as transsphenoidal hypophysectomy, create situations where an alternative route of administration is needed as in cases of nasal packing or recovery from surgery.
Save this treatment for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Tired of the same old research?
Check Latest Advances

Related Clinical Trials

Bleeding Reduction in Acute and Chronic KidnEy patienTs Having Surgery (BRACKETS) Pilot Trial

Summary: The BRACKETS pilot study is a multicentre, prospective, randomized controlled trial of prophylactic preoperative tranexamic acid (TXA) versus placebo and, using a partial factorial design, of prophylactic preoperative desmopressin versus placebo.

Phase II Prospective Evaluation of Desmopressin Stimulation Test Performance in ACTH-dependent Cushing s Syndrome

Background: Cushing syndrome (CS) is a set of diseases that develop when the body produces too much adrenocorticotropic hormone (ACTH). ACTH stimulates the production of a hormone called cortisol. Excess cortisol can cause serious issues, such as diabetes, high blood pressure, weight gain, and mood changes. Diagnosing CS early can be difficult. One test used to diagnose CS, the desmopressin (Desmo) stimulatio...

Desmopressin (DDAVP) Stimulation for 18F-FDG-PET Detection of Pituitary Adenoma in Cushing's Disease

Summary: This study is designed as a single institution trial. The study utilizes safe and clinically-validated tools for preoperative workup of patients with small pituitary tumors. DDAVP stimulation and 18F-labeled fluoro-deoxyglucose (FDG) uptake for PET-imaging will be used to detect MRI-negative pituitary adenomas in patients with Cushing s disease. Patients who have MRI-negative pituitary microadenom...

Brand Information

    DDAVP (Desmopressin Acetate)
    WARNING: HYPONATREMIA
    DDAVP can cause hyponatremia. Severe hyponatremia can be life-threatening, leading to seizures, coma, respiratory arrest, or death
    DDAVP is contraindicated in patients at increased risk of severe hyponatremia, such as patients with excessive fluid intake, illnesses that can cause fluid or electrolyte imbalances, and in those using loop diuretics or systemic or inhaled glucocorticoids
    Ensure the serum sodium concentration is normal before starting or resuming DDAVP. Measure serum sodium within 7 days and approximately 1 month after initiating therapy, and periodically during treatment. More frequently monitor serum sodium in patients 65 years of age and older and in patients at increased risk of hyponatremia
    If hyponatremia occurs, DDAVP may need to be temporarily or permanently discontinued
    1DOSAGE FORMS AND STRENGTHS
    Injection: DDAVP is a sterile, aqueous, colorless solution available as:
    • 4 mcg/mL in single-dose ampule
    • 40 mcg/10 mL (4 mcg/mL) in multiple-dose vial
    2CONTRAINDICATIONS
    DDAVP Injection is contraindicated in patients with known hypersensitivity to desmopressin acetate or to any of the components of DDAVP Injection
    DDAVP Injection is contraindicated in patients with the following conditions due to an increased risk of hyponatremia:
    • Moderate to severe renal impairment defined as a creatinine clearance below 50 mL/min
    • Hyponatremia or a history of hyponatremia
    • Known or suspected syndrome of inappropriate antidiuretic hormone (SIADH) secretion
    • Polydipsia
    • Concomitant use with loop diuretics
    • Concomitant use with systemic or inhaled glucocorticoids
    • During illnesses that can cause fluid or electrolyte imbalance, such as gastroenteritis, salt-wasting nephropathies, or systemic infection
    DDAVP Injection is contraindicated in patients with the following conditions because fluid retention increases the risk of worsening the underlying condition:
    • Heart failure
    • Uncontrolled hypertension
    3ADVERSE REACTIONS
    The following clinically significant adverse reactions are described elsewhere in the labeling:
    • Hyponatremia
    • Hypotension and Hypertension
    • Increased risk of thrombosis in patients with von Willebrand's Disease Type IIB
    • Hypersensitivity reactions
    • Fluid retention
    The following adverse reactions have been identified during post-approval use of DDAVP Injection. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.
    Cardiovascular: Hypertension, hypotension, tachycardia, thrombotic events, fluid retention
    4OVERDOSAGE
    Overdosage of DDAVP Injection leads to prolonged duration of action with an increased risk of water retention and hyponatremia. Signs of overdose may include headaches, abdominal cramps, nausea, facial flushing, confusion, drowsiness, problems with passing urine and rapid weight gain due to fluid retention
    There is no known specific antidote for desmopressin acetate or DDAVP Injection 4 mcg/mL.
    5DESCRIPTION
    DDAVP Injection (desmopressin acetate) is a synthetic vasopressin analog for intravenous or subcutaneous use. It is chemically defined as follows:
    Mol. Wt. 1183.34
    Empirical Formula: C
    Chemical Structure
    1-(3-mercaptopropionic acid)-8-D-arginine vasopressin monoacetate (salt) trihydrate.
    DDAVP solution for injection is a sterile solution in a 1 mL single-dose ampule: Each mL contains 4 mcg of desmopressin acetate which is equivalent to 3.6 mcg of desmopressin free base. The inactive ingredients are sodium chloride, hydrochloric acid and water for injection. Sodium chloride is used to adjust tonicity. Hydrochloric acid is used to adjust pH.
    DDAVP solution for injection is a sterile solution in a 10 mL multiple-dose vial: Each mL contains 4 mcg of desmopressin acetate which is equivalent to 3.6 mcg of desmopressin free base. The inactive ingredients are sodium chloride, chlorobutanol (5 mg per mL), hydrochloric acid and water for injection. Sodium chloride is used to adjust tonicity. Hydrochloric acid is used to adjust pH.
    6PRINCIPAL DISPLAY PANEL - 10 mL Vial Carton
    NDC 55566-2300-0
    Rx ONLY
    DDAVP
    desmopressin
    40 mcg/10 mL
    For Intravenous and
    One 10 mL
    FERRING
    PRINCIPAL DISPLAY PANEL - 10 mL Vial Carton
    7PRINCIPAL DISPLAY PANEL - 1 mL Ampule Carton
    NDC-55566-2200-0
    Rx ONLY
    DDAVP
    desmopressin
    4 mcg/mL
    PRESERVATIVE FREE
    Ten x 1 mL single-dose
    FERRING
    PRINCIPAL DISPLAY PANEL - 1 mL Ampule Carton
    DDAVP has been selected.