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Antidiuretic Hormone Analog/Discontinued

DIAPID

DIAPID

Clinical safety rating

caution

Comprehensive clinical and safety monograph for DIAPID (DIAPID).


What is DIAPID?

Comprehensive clinical and safety monograph for DIAPID (DIAPID).

Indications & Uses

Diabetes insipidus (central)Nocturnal enuresis (off-label)

Compare DIAPID vs CONCENTRAID →View all Antidiuretic Hormone Analog drugs →

Mechanism of Action

Diapid (lypressin) is a synthetic analog of vasopressin that acts as an antidiuretic by increasing water reabsorption in the renal collecting ducts via V2 receptor activation. It also has mild vasopressor activity via V1 receptor stimulation.

What the body does with it

MetabolismLypressin is rapidly metabolized by peptidases in the liver and kidneys, with a half-life of approximately 15 minutes.
ExcretionPrimarily renal excretion as unchanged drug (80-90%); minor biliary/fecal elimination (<10%)
Half-lifeTerminal elimination half-life is 1.5-3 hours; clinically significant in patients with renal impairment, requiring dose adjustment
Protein binding20-30% bound to plasma proteins
Volume of Distribution0.6-0.8 L/kg; distributes primarily in extracellular fluid
Bioavailability100% by intravenous route; Not bioavailable orally
Onset of ActionIntravenous: 1-2 minutes; Oral: Not applicable (IV use only)
Duration of ActionDuration is 10-30 minutes after IV bolus; titratable by continuous infusion
Molecular Weight445.55

Classification & Brands

Dosing & administration

Intravenous bolus of 20 mg followed by 20-40 mg every 2-4 hours as needed. Maximum single dose: 80 mg.

Dosage formSOLUTION
Renal impairmentNo adjustment required for GFR >30 mL/min. For GFR 10-30 mL/min: reduce dose by 50%. For GFR <10 mL/min: avoid use.
Liver impairmentChild-Pugh A: no adjustment. Child-Pugh B: reduce dose by 50%. Child-Pugh C: contraindicated.
Pediatric use0.2 mg/kg intravenously, repeat every 2 hours as needed. Maximum dose: 10 mg.
Geriatric useInitial dose of 10 mg intravenously, titrate cautiously due to increased sensitivity. Maximum single dose: 40 mg.

Use during pregnancy

1st trimesterDiapide (glipizide) is contraindicated in the first trimester due to potential teratogenic effects. Insulin is preferred for glycemic control during organogenesis.
2nd trimesterUse with caution in the second trimester; may be considered if insulin therapy is not feasible. Monitor for fetal hypoglycemia and macrosomia.
3rd trimesterUse with caution; increased risk of neonatal hypoglycemia. Discontinue at least 2 days before elective delivery to prevent prolonged neonatal hypoglycemia.

Clinical note

Comprehensive clinical and safety monograph for DIAPID (DIAPID).

Placental transferGlipizide crosses the placenta moderately, with fetal serum levels approximately 10-50% of maternal levels. It is not as extensively transported as glyburide.
BreastfeedingGlipizide is excreted into breast milk in low amounts. Although not expected to cause adverse effects in nursing infants, monitor for signs of hypoglycemia. Consider alternative agents with more safety data, such as glyburide or insulin.
Lactation RatingL3 (Moderately Safe)
Teratogenic RiskDiapide is contraindicated in pregnancy due to known teratogenic effects. First trimester exposure is associated with increased risk of congenital malformations, particularly cardiovascular and neural tube defects. Second and third trimester exposure may cause fetal hyperinsulinemia, macrosomia, and neonatal hypoglycemia.
Fetal MonitoringMonitor blood glucose levels in the mother. For fetal monitoring, consider ultrasound for fetal growth anomalies if exposed. Newborns should be monitored for hypoglycemia, jaundice, and electrolyte imbalances.
Fertility EffectsDiapide may impair fertility in females due to hormonal disturbances. In males, it may cause reversible spermatogenic suppression. Specific animal studies show reduced conception rates.

Warnings & precautions

■ FDA Black Box Warning

None.

Side Effect Profile

Serious Effects

Absolute Contraindications

Type 1 diabetes mellitusDiabetic ketoacidosis (with or without coma)Known hypersensitivity to glipizide or sulfonylureasSevere hepatic or renal impairment

Clinical Precautions

PrecautionsMonitor fluid and electrolyte balance to avoid water intoxication and hyponatremia., Use with caution in patients with coronary artery disease, hypertension, or renal impairment., May cause anaphylaxis or hypersensitivity reactions.
Food/DietaryNo significant food interactions. However, avoid excessive water intake and alcohol, which can affect ADH secretion.

Clinical Tips & Counseling

Clinical PearlsDiapid (desmopressin) is used for central diabetes insipidus and nocturnal enuresis. Monitor for hyponatremia, especially in elderly or patients with fluid/electrolyte imbalance. Avoid overhydration. Intranasal formulation may cause rhinitis or epistaxis.
Patient AdviceUse exactly as prescribed; do not exceed dose to avoid water intoxication. · Limit fluid intake to prevent hyponatremia (symptoms: headache, nausea, confusion). · For intranasal spray, gentle priming and alternating nostrils each dose. · Report signs of low sodium: severe headache, vomiting, muscle cramps, drowsiness.

DIAPID Interactions

Loading safety data…

This overview is compiled from peer-reviewed clinical sources and FDA labeling. It's here to support — not replace — clinical judgment. Always verify dosing against your institution's current protocols before prescribing.

On this page

Mechanism of ActionDosing & administrationUse during pregnancyWarnings & precautionsDrug interactions

Compare with

CONCENTRAIDDDAVPDDAVP (NEEDS NO REFRIGERATION)DESMODAMINIRIN

External sources

DailyMed (NIH) PubMed OpenFDA