If used to reduce spontaneous or traumatic bleeding, doses may be repeated after 8 hours to 12 hours and once daily thereafter, if needed, based upon clinical condition and von Willebrand factor and factor VIII levels. DDAVP, Stimate (desmopressin) dosing, indications, interactions The presence of platelet-vWF and normally functioning platelet glycoprotein (GP) IIb/IIIa seem to be essential for desmopressin's effect on platelets. eCollection 2022. Chlorpromazine: (Major) Additive hyponatremic effects may be seen in patients treated with desmopressin and drugs associated with water intoxication, hyponatremia, or SIADH including chlorpromazine. The woman had previously received desmopressin without the development of clinical symptoms of hyponatremia Meloxicam: (Major) Additive hyponatremic effects may be seen in patients treated with desmopressin and drugs associated with hyponatremia including NSAIDs. Preoperative doses may be given 2 hours prior to the scheduled procedure. Desmopressin can be started or resumed 3 days or 5 half-lives after the corticosteroid is discontinued, whichever is longer. Spironolactone; Hydrochlorothiazide, HCTZ: (Moderate) Monitor serum sodium more frequently during concomitant desmopressin and thiazide diuretic use due to increased risk of water intoxication with hyponatremia. A woman who took both desmopressin and ibuprofen was found in a comatose state. Response should be estimated by 2 parameters: adequate duration of sleep and adequate, not excessive, water turnover. Medically reviewed by Drugs.com. Use combination with caution, and monitor patients for signs and symptoms of hyponatremia. Flurbiprofen: (Major) Additive hyponatremic effects may be seen in patients treated with desmopressin and drugs associated with hyponatremia including NSAIDs. It is postulated that desmopressin-induced increases in FVIII and vWF are mediated through low-affinity, extrarenal V2 receptors. The woman had previously received desmopressin without the development of clinical symptoms of hyponatremia Methyclothiazide: (Moderate) Monitor serum sodium more frequently during concomitant desmopressin and thiazide diuretic use due to increased risk of water intoxication with hyponatremia. Blood samples were taken before and at predetermined time points up to 12 h after dosing. Repeat administration should be determined by laboratory response as well as the clinical condition of the patient. Fluid restrictions should be observed. Determine need for repeat dosage based on laboratory response and patient's clinical condition. Use combination with caution, and monitor patients for signs and symptoms of hyponatremia. As her serum sodium concentration was 121 mmol/L, and her plasma osmolality was low in the presence of a high-normal urine osmolality and normal sodium excretion, she was treated with fluid restriction. Of course, hypertonic bicarbonate could also be used, as discussed last week. Desmopressin can be started or resumed 3 days or 5 half-lives after the corticosteroid is discontinued, whichever is longer. Persons with renal disease may be at increased risk for low sodium concentrations, fluid overload, and electrolyte abnormalities. Brompheniramine; Carbetapentane; Phenylephrine: (Moderate) Although the pressor activity of desmopressin is very low compared to its antidiuretic activity, large doses of desmopressin should be used with other pressor agents like phenylephrine only with careful patient monitoring. A pharmacokinetic and pharmacodynamic comparison of desmopressin administered as whole, chewed and crushed tablets, and as an oral solution. As her serum sodium concentration was 121 mmol/L, and her plasma osmolality was low in the presence of a high-normal urine osmolality and normal sodium excretion, she was treated with fluid restriction. Selective serotonin reuptake inhibitors: (Minor) Additive hyponatremic effects may be seen in patients treated with desmopressin and drugs associated with water intoxication, hyponatremia, or SIADH including SSRIs. See Table 1 for volume of diluent to use. Fluid restriction should be observed, and fluid intake should be limited to a minimum from 1 hour before administration, until the next morning, or at least 8 hours after administration. DOSAGE AND ADMINISTRATION Hemophilia A and von Willebrand's Disease (Type I): Desmopressin Acetate Injection 4 mcg/mL is administered as an intravenous infusion at a dose of 0.3 mcg desmopressin acetate/kg body weight diluted in sterile physiological saline and infused slowly over 15 to 30 minutes. The use of desmopressin for nocturia is not recommended in pregnant women; nocturia is usually related to normal, physiologic changes during pregnancy that do not require treatment with desmopressin. 3 0 obj
Use combination with caution, and monitor patients for signs and symptoms of hyponatremia. 1.5-2 mg IM/SC = 6-7 mg PO. Dose range is 0.1 to 0.8 mg daily. Desmopressin | Davis's Drug Guide for Rehabilitation Professionals | F DDAVP/Desmopressin Injection - Summary of Product Characteristics (SmPC No statistically significant differences were detected between night and day except for terminal half-life, which was 3.1 h at night and 2.8 h in the daytime (P=0.02). A woman who took both desmopressin and ibuprofen was found in a comatose state. stream
TYPES OF IV TO PO THERAPY CONVERSIONS: There are three types of IV to PO therapy conversions as defi ned below: SEQUENTIAL THERAPY SWITCH THERAPY STEP DOWN THERAPY. Individualize dosing to prevent an excessive decrease in plasma osmolality, which can lead to hyponatremia and possible seizures. Use combination with caution, and monitor patients for signs and symptoms of hyponatremia. The woman had previously received desmopressin without the development of clinical symptoms of hyponatremia Oxybutynin: (Major) Hyponatremia-induced convulsions have been rarely reported when oxybutynin and desmopressin are used concomitantly. Treatment with ddAVP improves platelet-based coagulation in a rat model of traumatic hemorrhagic shock. The effect of DDAVP was measured on F VIII/vWF complex and on plasminogen activator release. Use combination with caution, and monitor patients for signs and symptoms of hyponatremia. Desmopressin may promote an increased exposure of platelet vWF to GPIIb/IIIa on the platelet surface upon activation of the platelet. 1/10 of intranasal dose . eCollection 2022. 1997;183:53-4. The pump will stay primed for up to 1 week. administration route. Desmopressin is found in breast milk, but not in significant amounts. Her serum sodium concentration was 124 mmol/L within a day and was 135 mmol/L by the second day. Hemophilia A and von Willebrand's Disease (Type I): The recommended dosage is 0.3 mcg/kg actual body weight (to a maximum of 20 mcg) administered by intravenous infusion over 15 minutes to 30 minutes. The recommended maintenance dose is 10 mcg/day to 40 mcg/day intranasally (0.1 mL/day to 0.4 mL/day) in 1 to 3 divided doses. During initial titration and continued therapy, observe and monitor closely; adjust treatment to the diurnal pattern of response. Fluid restriction was to be observed, with fluid intake was limited to a minimum from 1 hour before intranasal administration, until the next morning, or at least 8 hours after administration. The woman had previously received desmopressin without the development of clinical symptoms of hyponatremia Diflunisal: (Major) Additive hyponatremic effects may be seen in patients treated with desmopressin and drugs associated with hyponatremia including NSAIDs. 1:2. Fatal anaphylaxis has been reported with intravenous desmopressin. Guaifenesin; Phenylephrine: (Moderate) Although the pressor activity of desmopressin is very low compared to its antidiuretic activity, large doses of desmopressin should be used with other pressor agents like phenylephrine only with careful patient monitoring. Use in children requires careful fluid intake restrictions to prevent possible hyponatremia and water intoxication. Prior to treatment with DDAVP Injection, verify that factor VIII coagulant activity levels are >5% and exclude the presence of factor VIII autoantibodies. Use combination with caution, and monitor patients for signs and symptoms of hyponatremia. In additio Initiate at low dose and increase as necessary. Flunisolide: (Major) Desmopressin is contraindicated with concomitant inhaled or systemic corticosteroid use due to an increased risk of hyponatremia. Greatly enhanced ADH activity. Dosage form: injection In general, desmopressin is contraindicated in persons with heart failure or uncontrolled hypertension because fluid retention increases the risk for worsening of underlying conditions that are susceptible to volume status. Heparin: (Minor) Desmopressin has been shown to have an additive effect on the anticoagulant activity of heparin. After oral desmopressin, concentrations above the limit of quantification (2.5 pg/ml) were only detected in 51% of the samples. As her serum sodium concentration was 121 mmol/L, and her plasma osmolality was low in the presence of a high-normal urine osmolality and normal sodium excretion, she was treated with fluid restriction. Intranasal: <>
Desmopressin can be started or resumed 3 days or 5 half-lives after the corticosteroid is discontinued, whichever is longer. Administration of intranasal desmopressin may be compromised by nasal mucosa changes (e.g., nasal trauma, nasal surgery, nasal blockage, nasal mucosal atrophy, congestion, or severe atrophic rhinitis), cranial surgery, and nasal packing. Diabetes Insipidus: < 12 years: No definitive dosing available. Desmopressin is administered intravenously or subcutaneously.Desmopressin (DDAVP) injection has an antidiuretic hormone activity of 16 International Units/mL; 1 mcg desmopressin is equivalent to 4 International Units antidiuretic hormone activity.If given preoperatively, desmopressin injection should be given 30 minutes before the scheduled procedure.Visually inspect parenteral products for particulate matter and discoloration prior to administration whenever solution and container permit. Subscribe to Drugs.com newsletters for the latest medication news, new drug approvals, alerts and updates. BJU Int. Demonstration of an adequate improvement in coagulation profile after administration is recommended prior to any surgical procedures. Use combination with caution, and monitor patients for signs and symptoms of hyponatremia. In a single study of postpartum women receiving a single dose of intranasal desmopressin, a marked change in plasma concentration of desmopressin was seen; however, little, if any, change in assayable desmopressin was found in breast milk. Then i-Vents acuity will now have a 10 to signify there is a open i-Vent. This increase is dose-dependent, with an IV dosage of 0.4 mcg/kg producing a 300% to 400% maximum increase in Factor VIII activity. Vasopressin also causes constriction of vascular smooth muscle and contraction of smooth muscle in the GI tract and uterus. This site needs JavaScript to work properly. Monitor serum sodium concentrations within 1 week and then approximately 1 month after treatment initiation and periodically thereafter. However, individualized dosing is recommended due to high inter-patient variability in response. In the elderly, careful dosage selection and monitoring of renal function are recommended. Her serum sodium concentration was 124 mmol/L within a day and was 135 mmol/L by the second day. The 0.83 mcg dose did not meet all prespecified efficacy endpoints in clinical trials, but may have a lower risk of hyponatremia. Intranasal: 1 spray (1.5 mg/mL) in each nostril one time. Typical maintenance dose was 10 to 40 mcg/day (0.1 to 0.4 mL/day). Her serum sodium concentration was 124 mmol/L within a day and was 135 mmol/L by the second day. Neither GlobalRPh Inc. nor any other party involved in the preparation of this document shall be liable for any special, consequential, or exemplary damages resulting in whole or part from any user's use of or reliance upon this material. Two children with diabetes insipidus had decreasing desmopressin requirements with lamotrigine initiation. If doses other than these are required, the rhinal tube delivery system may be used.One spray (10 mcg) has an antidiuretic activity of about 40 International Units.The nasal spray must be primed prior to first use. Desmopressin can be started or resumed 3 days or 5 half-lives after the corticosteroid is discontinued, whichever is longer. PDF Intravenous Medication Guidelines for Adults - VCHCA ! Limit fluid intake to a minimum 1 hour before and 8 hours after administration. Patients previously receiving intranasal treatment may begin oral therapy the night following (24 hours) the last intranasal dose. The volume of diluent is weight-based. The easiest way to lookup drug information, identify pills, check interactions and set up your own personal medication records. 4 0 obj
The nasal spray should not be used to treat patients with type IIB von Willebrand's disease since platelet aggregation may be induced. 150 mcg into each nostril once for a total dose of 300 mcg. If the product has not been used for more than 3 days, re-prime by pumping 2 actuations into the air.Instruct the patient to blow their nose, tilt the head back slightly, and insert the nasal applicator into the left or right nostril, keeping the nasal applicator upright. Desmopressin is a man-made form of vasopressin and is used to replace a low level of vasopressin. Initially, 0.05 mg PO once daily. Levels of FVIII are also increased, which increases hemostasis by accelerating fibrin formation. Adjust dose based upon response to treatment estimated by two parameters: adequate duration of sleep and adequate, not excessive, water turnover. e-N;CM_[9,jPUO'@O%W]I,7wO;~ -O{GOiZb]]qJy=q4/I3>1&p#!EoA2hF"H kn.u,yQg Prilocaine; Epinephrine: (Minor) The antidiuretic response to desmopressin may be reduced in patients receiving high doses of epinephrine concomitantly. However, the amount of orally administered drug reduced for its i.p., i.m., s.c., or i.v. Demonstration of an adequate improvement in coagulation profile after administration is recommended prior to any surgical procedures. The woman had previously received desmopressin without the development of clinical symptoms of hyponatremia Candesartan; Hydrochlorothiazide, HCTZ: (Moderate) Monitor serum sodium more frequently during concomitant desmopressin and thiazide diuretic use due to increased risk of water intoxication with hyponatremia. As of 2007 in response to a FDA request for removal of the indication, the intranasal formulation is no longer indicated for the treatment of primary nocturnal enuresis secondary to post-marketing reports of hyponatremic-related seizures, which most often occurred in pediatric patients. Diabetes insipidus: 2-4 mcg/day IV push or SC. Desmopressin is also used to control bed-wetting. Fill in the blank - Do not enter the label - Rounding - Verify answer - Conversions - Practice questions. I would recommend making an appointment with your regular doctor to see what might be causing this. Desmopressin is a strong V2 agonist and has no effect on V1 receptors. Her serum sodium concentration was 124 mmol/L within a day and was 135 mmol/L by the second day. Her serum sodium concentration was 124 mmol/L within a day and was 135 mmol/L by the second day. Initial dose: 0.05 mg orally twice a day or Noctiva Nasal SprayNoctiva nasal spray delivers either 0.83 mcg or 1.66 mcg of desmopressin acetate (equivalent to 0.75 mcg or 1.5 mcg of desmopressin) per spray (0.1 mL).Two sprays of the 0.83 mcg nasal spray are not interchangeable with 1 spray of the 1.66 mcg nasal spray; the 1.66 mcg/0.1 mL nasal spray should be prescribed for patients who are or will be taking the 1.66 mcg dose.Do NOT shake the bottle.Prime the nasal spray before using for the first time by pumping 5 actuations into the air away from the face. Maximal dose-response increase in Factor VIII activity occurs at 0.3 to 0.4 mcg/kg desmopressin. PLEASE READ THE. Usual Adult Dose for Diabetes Insipidus Initial dose: 0.05 mg orally twice a day or 1 to 2 mcg IV twice a day or 1 to 2 mcg subcutaneously twice a day or 5 to 40 mcg spray intranasally twice a day or 0.1 to 0.4 mL via rhinal tube intranasally twice a day. Desmopressin, sold under the trade name DDAVP among others, is a medication used to treat diabetes insipidus, bedwetting, hemophilia A, von Willebrand disease, and high blood urea levels. Amiloride; Hydrochlorothiazide, HCTZ: (Moderate) Monitor serum sodium more frequently during concomitant desmopressin and thiazide diuretic use due to increased risk of water intoxication with hyponatremia. DDAVP, Minirin, Nocdurna, Stimate, +2 more. Olmesartan; Hydrochlorothiazide, HCTZ: (Moderate) Monitor serum sodium more frequently during concomitant desmopressin and thiazide diuretic use due to increased risk of water intoxication with hyponatremia. Drugs.com provides accurate and independent information on more than 24,000 prescription drugs, over-the-counter medicines and natural products. Twist off the seal from the dropper. For the treatment of hypothyroidism of any etiology, except during the recovery phase of subacute thyroiditis; used as a replacement in primary (thyroidal), secondary (pituitary), tertiary (hypothalamic), congenital (cretinism), or acquired hypothyroidism. In general, most reported clinical experience with desmopressin has not identified efficacy response differences between geriatric and younger patients. -, Br J Urol. Careers. Most patients respond to 1 to 2 doses; administer a second dose 8 to 24 hours after the first dose if needed. Store refrigerated 2 to 8C (36 to 46F). Her serum sodium concentration was 124 mmol/L within a day and was 135 mmol/L by the second day. It may be given in the nose, by injection into a vein, by mouth, or under the tongue. Sulindac: (Major) Additive hyponatremic effects may be seen in patients treated with desmopressin and drugs associated with hyponatremia including NSAIDs. The woman had previously received desmopressin without the development of clinical symptoms of hyponatremia Indomethacin: (Major) Additive hyponatremic effects may be seen in patients treated with desmopressin and drugs associated with hyponatremia including NSAIDs.
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