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DDAVP NASAL SPRAY (DESMOPRESSIN ACETATE): WARNINGS
DDAVP Nasal Spray (Desmopressin Acetate) is for intranasal use only.
DDAVP Nasal Spray should only be used in patients where orally administered formulations are not feasible.
Very rare cases of hyponatremia have been reported from world-wide postmarketing experience in patients treated with DDAVP (Desmopressin Acetate). This drug is a potent antidiuretic which, when administered, may lead to water intoxication and/or hyponatremia.
Unless properly diagnosed and treated hyponatremia can be fatal. Therefore, fluid restriction is recommended and should be discussed with the patient and/or guardian. Careful medical supervision is required.
When DDAVP Nasal Spray (Desmopressin) is administered, in particular in pediatric and geriatric patients, fluid intake should be adjusted downward in order to decrease the potential occurrence of water intoxication and hyponatremia. All patients receiving DDAVP Nasal Spray (Desmopressin Acetate) therapy should be observed for the following signs or symptoms associated with hyponatremia: headache, nausea/vomiting, decreased serum
sodium weight gain, restlessness, fatigue, lethargy, disorientation, depressed reflexes, loss of appetite, irritability, muscle weakness, muscle spasms or cramps and abnormal mental status such as hallucinations, decreased consciousness and confusion. Severe symptoms may include one or a combination of the following: seizure, coma and/or respiratory arrest. Particular attention should be paid to the possibility of the rare occurrence of an extreme decrease in plasma osmolality that may result in seizures which could lead to coma.
DDAVP (Desmopressin) Nasal Spray should be used with caution in patients with habitual or psychogenic polydipsia who may be more likely to drink excessive amounts of water, putting them at greater risk of
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DDAVP Nasal Spray prescribing information
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