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Vasopressin Market Size, Share & Trends Analysis Report By Type (Intravenous Injection, Intramuscular Injection, And Subcutaneous Injection), Application (Vasodilatory Shock, Anti-Diuretic Hormone Deficiency, Ventricular Tachycardia & Fibrillation, And Gastrointestinal Bleeding), Region (North America, Europe, Asia-Pacific, Middle East & Africa, and South America)—Forecast till 2028

Categories: Life Science

Formate :

The global Vasopressin market is valued at 1004.6 million US$ in 2021 and is expected to grow at a CAGR of 14.5% during 2021-2026.


Vasopressin, likewise called antidiuretic hormone (ADH), arginine vasopressin (AVP), or argipressin is a hormone integrated as a peptide prohormone in neurons in the nerve center, and is changed over to AVP. It at that point goes down the axon of that cell, which ends in the back pituitary, and is delivered from vesicles into the flow because of extracellular liquid hypertonicity (hyperosmolality). AVP has two essential capacities. To begin with, it builds the measure of without solute water reabsorbed once again into the flow from the filtrate in the kidney tubules of the nephrons. Second, AVP tightens arterioles, which expands fringe vascular obstruction and raises blood vessel pulse. A third capacity is conceivable. Some AVP might be delivered legitimately into the mind from the nerve center and may assume a significant function in social conduct, sexual inspiration, and pair holding, and maternal reactions to push. Vasopressin actuates the separation of undifferentiated cells into cardiomyocytes and advances heart muscle homeostasis. It has a short half-life, between 16–24 minutes.


Vasopressin is an enemy of the diuretic hormone. It is found in many warm-blooded animals, and its function as the water-managing particle has been known for a very long time. Vasopressin is a nine amino corrosive peptide discharged from the back pituitary. The antidiuretic hormone binds to receptors in the kidney's distal or collecting tubules, promoting water reabsorption back into the circulation. It is utilized to treat diabetes insipidus and certain states of the stomach after medical procedures or during stomach x-beams. It is infused into a muscle or under the skin, or into a vein through an IV.


Antidiuretics tie with receptor cells present in the kidney and increment water reabsorption by animating aquaporins present in layers of kidney tubules. These aquaporins transport solute-free water from the tubules to the blood by diminishing the osmolality of plasma cells. As the grouping of plasma cells builds, the pace of antidiuretic hormone discharge increments in the blood which expands the reabsorption of water. This builds water maintenance and pee focus. Insufficiency of antidiuretic hormones causes two kinds of diabetes insipidus: cranial diabetes insipidus and nephrogenic diabetes insipidus. The manifestations of diabetes insipidus are increments in water admission to remunerate the loss of water. In uncommon circumstances, diabetes insipidus can create during pregnancy and lead to gastrointestinal diabetes insipidus.


Cranial diabetes happens when there isn't sufficient antidiuretic hormone present in the body to control pee creation. It is the most widely recognized sort of diabetes insipidus which happens when the pituitary organ or the nerve center doesn't work appropriately. Nephrogenic diabetes insipidus happens when the kidneys neglect to work appropriately within the sight of antidiuretic hormone. It is caused because of kidney glitch. To treat diabetes insipidus, desmopressin and vasopressin are utilized which recreate the capacity of antidiuretic hormone work. The most widely recognized meds utilized for the treatment of nephrogenic diabetes insipidus are thiazide diuretics, which help to diminish the measure of pee created by the kidney. The acquired type of nephrogenic diabetes insipidus is because of change in AVPR quality, in exceptionally uncommon cases roughly 10% of acquired diabetes insipidus results from the transformation in aquaporin 2 quality. The obtained type of nephrogenic diabetes insipidus can prompt blister arrangement in the kidney, high calcium levels in the blood, and lead to kidney diseases.


The predominance pace of diabetes insipidus in the U.S. is around 1 of every 6,666, while the pervasiveness pace of diabetes insipidus among the all-inclusive community is roughly 1 out of 25,000 people. Significant drivers of the Vasopressin market are developing mindfulness, the rising pervasiveness of diabetes, expanding geriatric populace, increment in stoutness in the youthful age, and government activities to elevate research identified with the investigation of antidiuretics and their utilization to control diabetes insipidus. The significant expense related with the medication, rigid administrative situations in drug improvement, hazard factors related to antidiuretics, for example, over the top dying, wooziness, and hematoma during an assortment of a blood tests from people on diuretics are probably going to limit the antidiuretics market during the figure time frame. 


The global market is divided into three categories: type, application, and geography. Based on type, the global market is segmented into intravenous injection, intramuscular injection, and subcutaneous injection. Based on application, the global market is divided into vasodilatory shock, anti-diuretic hormone deficiency, ventricular tachycardia & fibrillation, and gastrointestinal bleeding. Based on region, the global market is segmented into North America, Europe, Asia Pacific, the Middle East and Africa, and South America.


Major players in the global market include Pfizer, Novartis AG, F Hoffmann-La Roche, bioMérieux, Merck & Co., Sanofi, Cayman Chemical, and JHP Pharmaceuticals LLC, Fresenius Kabi Canada, Par Pharmaceutical, Ferring Pharmaceuticals, Shanghai Soho-Yiming Pharmaceuticals, Astellas Pharma, and others.

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Vasopressin Market Size, Share & Trends Analysis R...

RD Code : HP21