Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Desmopressin
Drug ID BADD_D00616
Description Desmopressin (dDAVP), a synthetic analogue of 8-arginine vasopressin (ADH), is an antidiuretic peptide drug modified by deamination of 1-cysteine and substitution of 8-L-arginine by 8-D-arginine. ADH is an endogenous pituitary hormone that has a crucial role in the control of the water content in the body. Upon release from the stimulation of increased plasma osmolarity or decreased circulating blood volume, ADH mainly acts on the cells of the distal part of the nephron and the collecting tubules in the kidney [T28]. The hormone interacts with V1, V2 or V3 receptors with differing signal cascade systems. Desmopressin displays enhanced antidiuretic potency, fewer pressor effects due to V2-selective actions, and a prolonged half-life and duration of action compared to endogenous ADH [A31661]. It has been employed clinically since 1972 and is available in various formulations including intranasal solution, intravenous solution, oral tablet and oral lyophilisate [A31662]. Desmopressin is indicated for the treatment of polyuric conditions including primary nocturnal enuresis, nocturia, and diabetes insipidus. It was also newly approved for the treatment of mild classical hemophilia and von Willebrand's disease for minor surgeries. The active ingredient in most formulations is desmopressin acetate. Nocdurna, or desmopressin acetate, was approved by the FDA on June 21st, 2018 for the treatment of nocturia due to nocturnal polyuria in adults. It is available as a sublingual tablet.
Indications and Usage - Indicated for the treatment of nocturia due to nocturnal polyuria in adults who awaken at least 2 times per night to void (intranasal). - Indicated as antidiuretic replacement therapy in the management of central cranial diabetes insipidus and for management of the temporary polyuria and polydipsia following head trauma or surgery in the pituitary region (intranasal/parenteral). - Indicated for patients with hemophilia A with factor VIII coagulant activity levels greater than 5% or mild to moderate classic von Willebrand's Disease (Type I) with factor VIII levels greater than 5% during surgical procedures and postoperatively to maintain hemostasis (parenteral).
Marketing Status approved
ATC Code H01BA02
DrugBank ID DB00035
KEGG ID D00291
MeSH ID D003894
PubChem ID 5311065
TTD Drug ID D0U7SH
NDC Product Code 41701-007; 62938-0023; 52416-108; 52416-115; 60870-0440; 62938-0024
UNII ENR1LLB0FP
Synonyms Deamino Arginine Vasopressin | Arginine Vasopressin, Deamino | 1-Desamino-8-arginine Vasopressin | Vasopressin, 1-Desamino-8-arginine | Desmopressin | Vasopressin, Deamino Arginine | 1-Deamino-8-D-arginine Vasopressin | Vasopressin, 1-Deamino-8-D-arginine | Adiuretin SD | Apo-Desmopressin | DDAVP | Octostim | Desmotabs | Octim | Desmopressine Ferring | Ferring, Desmopressine | Desmospray | Nocutil | Desmopressin Acetate | Acetate, Desmopressin | Desmopressin Monoacetate, Trihydrate | Monoacetate, Trihydrate Desmopressin | Trihydrate Desmopressin Monoacetate | Desmopressin Monoacetate | Monoacetate, Desmopressin | Minirin | Minurin | Adiuretin | Desmogalen
Chemical Information
Molecular Formula C46H64N14O12S2
CAS Registry Number 16679-58-6
SMILES C1CC(N(C1)C(=O)C2CSSCCC(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N2)CC(=O)N)CCC(=O)N)C C3=CC=CC=C3)CC4=CC=C(C=C4)O)C(=O)NC(CCCN=C(N)N)C(=O)NCC(=O)N
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice.
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Thrombocytopenia01.08.01.0020.000855%-
Thrombosis24.01.01.006---
Tinnitus04.04.01.002; 17.04.07.004--
Unresponsive to stimuli17.02.05.0310.000855%-
Upper respiratory tract infection11.01.13.009; 22.07.03.011--
Urethral disorder20.07.01.002---
Urinary incontinence17.05.01.008; 20.02.02.0100.001882%
Urinary retention20.02.02.011--
Urinary tract disorder20.08.01.001---
Urticaria10.01.06.001; 23.04.02.001--
Vertigo04.04.01.003; 17.02.12.002--
Visual impairment06.02.10.013---
Vomiting07.01.07.0030.002566%
Water intoxication05.03.03.003; 14.05.06.004; 19.07.03.0040.002138%-
Weight increased13.15.01.006--
Wheezing22.03.01.009--
Brain oedema12.01.10.010; 17.07.02.0030.001283%
Eye oedema06.08.03.013---
Eye pruritus06.04.05.006---
Nasal discomfort22.12.03.012---
Musculoskeletal discomfort15.03.04.001---
Inappropriate antidiuretic hormone secretion05.03.03.001; 14.05.07.0010.002566%-
Affect lability19.04.01.001---
Cognitive disorder17.03.03.003; 19.21.02.0010.000855%
Vasodilation procedure25.03.01.001---
Angiopathy24.03.02.007---
Hepatic enzyme increased13.03.04.028---
Bladder disorder20.03.01.002---
Cardiac disorder02.11.01.003---
Connective tissue disorder10.04.04.026; 15.06.01.006---
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ADReCS-Target
Drug Name ADR Term Target
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