Synonym |
DDAVP |
Species |
Human |
Protein Accession |
P01160 |
Purity |
Greater than 95% as determined by SDS-PAGE |
Endotoxin Level |
Less than 1 EU/μg |
Biological Activity |
The activity was determined by measuring the concentration of cAMP that was produced by cells
after incubation with Desmopressin Acetate. The EC50 for this effect is typically 0.1-0.3 ng/mL.
|
Expression System |
E. coli |
Fusion Tag |
None |
Predicted Molecular Mass |
10608 Da |
Formulation |
Lyophilized from a 0.2 μm filtered solution of acetonitrile and TFA |
Reconstitution |
It is recommended to reconstitute the lyophilized Desmopressin Acetate in sterile 18 MΩ-cm H2O
not less than 100 µg/ml, which can then be further diluted to other aqueous solutions. |
Storage & Stability |
Store at -20°C upon receipt. A reconstitution is recommended to carry out in dark and cool area.
|
FAQ
What is Desmopressin Acetate and how does it work?
Desmopressin Acetate is a synthetic analog of
the natural hormone vasopressin. It plays an essential role in regulating the body’s water balance and
is commonly utilized in treating conditions that require the reduction of urine production. The primary
function of Desmopressin Acetate is to mimic the natural action of vasopressin, which involves
concentrating the urine and decreasing urine output. By binding to the V2 receptors in the renal
collecting ducts, Desmopressin Acetate prompts the reabsorption of water from the urine into the
kidney’s collecting duct system. This results in less frequent urination and reduced night-time
urination episodes, alleviating the symptoms of certain medical conditions including nocturnal enuresis
(bedwetting), diabetes insipidus, and certain clotting disorders like hemophilia A and von Willebrand's
disease.
Another critical benefit of Desmopressin Acetate is its role in increasing the levels of
coagulation factor VIII and von Willebrand factor in individuals who have certain bleeding disorders. It
achieves this through stimulating the release of these factors from the cells in which they are stored.
In doing so, Desmopressin Acetate provides a temporary boost to the clotting ability of a patient’s
blood, which is particularly useful in situations where spontaneous bleeding or excessive bleeding
during surgery could occur.
Furthermore, the advantage of using Desmopressin Acetate over natural
vasopressin is that it usually comes with fewer side effects, owing to its selective mechanism of action
mainly targeting the V2 receptors in renal tissue, while sparing the V1a receptors that are associated
with vasoconstriction and potential cardiovascular effects. This makes it a safer and more targeted
choice for patients requiring control over their water balance without the risk of causing hypertension
or other cardiovascular issues.
For patients experiencing issues related to desmopressin's
primary applications, this medication can provide notable improvements in quality of life, offering a
means to manage and mitigate the symptoms effectively. It is crucial, however, to engage with healthcare
professionals to determine the appropriateness of Desmopressin Acetate for each individual’s specific
health context and to ascertain the right dosing regimen to optimize effectiveness and
safety.
What conditions are treated with Desmopressin Acetate?
Desmopressin Acetate is a
versatile medication used to treat a variety of conditions that typically involve excessive urine
production or specific blood clotting disorders. Primarily, it is effective in managing central diabetes
insipidus, a condition in which the kidneys are unable to conserve water due to insufficient production
or action of the hormone vasopressin. This condition leads to excessive urine production and frequent
thirst, significantly impacting the patient’s hydration and comfort. By administering Desmopressin
Acetate, the patient’s ability to concentrate urine is restored, reducing urine output and normalizing
thirst.
Additionally, Desmopressin Acetate is widely applied in treating nocturnal enuresis or
bedwetting in children and adults. This condition can be distressing, often linked to the inability to
concentrate urine during nighttime hours. The drug effectively decreases the frequency of urination at
night and consequently minimizes bedwetting episodes, offering significant relief and improved sleep
quality for patients.
Another important use of Desmopressin Acetate is in the management of
certain bleeding disorders, specifically mild to moderate hemophilia A and von Willebrand's disease. In
these scenarios, the medication acts to increase the levels of clotting factor VIII and von Willebrand
factor, which are deficient or dysfunctional in affected individuals. This increase helps to improve
blood clotting capacity temporarily, which is particularly valuable during surgical procedures or to
manage spontaneous bleeding episodes.
In some cases, Desmopressin Acetate is also prescribed for
patients with renal concentrating defects that do not respond adequately to other forms of treatment,
offering an alternative for managing their symptoms effectively. It is imperative for healthcare
providers to assess each individual's eligibility for Desmopressin Acetate, considering potential
contraindications and ensuring that the therapy aligns well with the patient’s comprehensive care plan.
What are the potential side effects of taking Desmopressin Acetate?
While Desmopressin
Acetate is generally well tolerated, like any medication, it may cause side effects in some individuals.
The most significant risk associated with the use of Desmopressin Acetate is the possibility of
developing hyponatremia, a condition characterized by abnormally low levels of sodium in the blood.
Hyponatremia can arise due to the excessive reabsorption of water mediated by the drug, leading to an
imbalance in the body's electrolytes. Symptoms of hyponatremia may include headache, nausea, vomiting,
muscle cramps, and in severe cases, confusion, seizures, or coma. Therefore, monitoring sodium levels
and fluid intake is crucial for patients undergoing Desmopressin Acetate therapy, especially in the
early stages of treatment or during any dose adjustments.
Apart from hyponatremia, other side
effects may include headache, dizziness, and fatigue, which can occur as the body adjusts to the
medication. Many of these side effects tend to be mild and may resolve as treatment continues. Some
patients may also experience abdominal pain or nausea, which can be managed by adjusting the dosage or
timing of medication intake, under the guidance of a healthcare provider.
More rare but serious
side effects can include allergic reactions, characterized by rash, itching, swelling, severe dizziness,
or trouble breathing. It is imperative for patients to seek immediate medical attention if they
experience any signs of an allergic reaction.
Desmopressin Acetate can also interact with other
medications, leading to potential side effects or reduced effectiveness of either the desmopressin or
the concomitant medicine. Commonly interacting drugs include certain pain medications, antipsychotics,
antidepressants, and carbamazepine, which can enhance the antidiuretic effect of Desmopressin, thus
intensifying the risk of hyponatremia. It is vital to inform the healthcare provider of all the
medications and supplements currently being taken to minimize the risk of adverse
interactions.
Overall, while the benefits of Desmopressin Acetate in treating its indicated
conditions are substantial, vigilance is necessary to identify and mitigate potential side effects as
part of a comprehensive therapeutic strategy. Regular follow-up appointments with healthcare providers
are essential to ensure that the balance between efficacy and safety is maintained.
How should
Desmopressin Acetate be taken?
The administration of Desmopressin Acetate must be tailored to the
specific condition being treated and the individual characteristics of the patient. It is crucial for
the medication to be taken as prescribed by a healthcare professional, with close adherence to the
recommended dosage and schedule. Desmopressin Acetate comes in various forms, including oral tablets,
nasal sprays, and injectables, offering flexibility based on patient preference and the intended
use.
For conditions like central diabetes insipidus, Desmopressin Acetate is often administered
orally or via a nasal spray. Patients are advised to follow the precise instructions regarding the
timing and amount of each dose. Since the dosage may vary depending on factors such as age, weight, and
the severity of symptoms, it is essential to not make any adjustments without consulting a healthcare
provider.
In cases of nocturnal enuresis, the medication is usually taken once daily, typically
in the evening, to control urine production during the night and effectively reduce bedwetting episodes.
Patients must follow specific guidance on fluid intake restriction around the time of administration to
prevent overhydration and the associated risk of hyponatremia.
For bleeding disorders such as
hemophilia A and von Willebrand's disease, Desmopressin Acetate may be given as needed ahead of surgical
procedures or when there is evidence of bleeding. The mode of administration may be oral, intranasal, or
intravenously, depending on the clinical scenario and urgency.
A critical aspect of taking
Desmopressin Acetate is monitoring fluid intake, as excessive water consumption can lead to serious
complications, including hyponatremia. Patients are often advised to limit their fluid intake from one
hour before to eight hours after administration. This helps to maintain the delicate balance between
therapeutic efficacy and the minimization of adverse effects.
Missed doses should be handled
carefully. If a dose is missed, patients should take it as soon as they remember, unless it is close to
the time of the next scheduled dose. Doubling up on doses to make up for a missed one is typically not
recommended and should be discussed with a healthcare provider.
Finally, ongoing communication
with a healthcare provider is paramount. Regular follow-up visits may be needed to monitor the
effectiveness of the treatment, adjust doses if necessary, and check for any adverse effects, ensuring
optimal management of the patient's condition. By adhering strictly to the guidelines provided by
healthcare professionals and maintaining open lines of communication, patients can safely benefit from
the therapeutic effects of Desmopressin Acetate.
Who should not take Desmopressin
Acetate?
Desmopressin Acetate, while beneficial for many patients, is not suitable for everyone.
Individuals with certain medical conditions or risk factors may be advised against taking this
medication due to potential complications or ineffective outcomes. Primarily, those with a history of
hyponatremia should generally avoid Desmopressin Acetate, because the drug’s action in promoting water
reabsorption and reducing urine output can exacerbate low sodium levels, leading to potentially
dangerous conditions like seizures or coma.
Patients with moderate to severe renal impairment are
typically not candidates for Desmopressin Acetate. The drug is processed by the kidneys, and impaired
renal function can lead to decreased drug clearance and an increased risk of adverse effects such as
water intoxication and severe electrolyte imbalance. Additionally, those with a history of heart failure
or other conditions that cause fluid and electrolyte disturbances should use Desmopressin Acetate with
caution and under strict medical supervision.
Desmopressin Acetate is also not recommended for
individuals with known hypersensitivity to desmopressin or any of the inactive ingredients in the
formulation. Severe allergic reactions can occur if administered to those with such sensitivities,
hence, it is crucial to communicate any known allergies with healthcare providers prior to starting
treatment.
Furthermore, patients with polydipsia (habitual excessive drinking of fluids), whether
psychogenic or secondary to a condition like uncontrolled diabetes mellitus, may not respond well to
Desmopressin Acetate. The excessive fluid intake can lead to dilutional hyponatremia, which the
medication might aggravate, resulting in serious hyponatremic complications.
Pregnant or
breastfeeding women should discuss with their healthcare provider before starting Desmopressin Acetate.
Although some studies have not shown significant risk, the full effects of desmopressin on fetal
development and lactation remain not completely understood. Healthcare providers can help weigh the
benefits against any potential risks to ensure the safety of both the mother and the
child.
Ultimately, the determination of whether Desmopressin Acetate is appropriate for a patient
must be made in consultation with a healthcare provider. By thoroughly evaluating the patient’s entire
health profile and any existing medical conditions, healthcare professionals can provide personalized
guidance and recommendations, aiming to maximize therapeutic outcomes while minimizing potential risks.
Regular monitoring and communication are essential components of safely managing treatment with
Desmopressin Acetate.