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Pronunciation |
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(dye
hye droe tak IS ter
ole) |
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U.S. Brand
Names |
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DHT™; Hytakerol® |
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Generic
Available |
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Yes |
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Synonyms |
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Dichysterol |
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Pharmacological Index |
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Vitamin D Analog |
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Use |
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Treatment of hypocalcemia associated with hypoparathyroidism; prophylaxis of
hypocalcemic tetany following thyroid surgery |
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Pregnancy Risk
Factor |
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A/D (if dose exceeds RDA recommendation) |
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Contraindications |
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Hypercalcemia, known hypersensitivity to
dihydrotachysterol |
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Warnings/Precautions |
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Calcium-phosphate product (serum calcium and phosphorus) must not exceed 70;
avoid hypercalcemia; use with caution in coronary artery disease, decreased
renal function (especially with secondary hyperparathyroidism), renal stones,
and elderly |
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Adverse
Reactions |
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>10%:
Endocrine & metabolic: Hypercalcemia
Renal: Elevated serum creatinine, hypercalciuria
<1%: Convulsions, polydipsia, nausea, vomiting, anorexia, weight loss,
polyuria, anemia, weakness, metastatic calcification, renal damage
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Overdosage/Toxicology |
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Symptoms of overdose include hypercalcemia, anorexia, nausea, weakness,
constipation, diarrhea, vague aches, mental confusion, tinnitus, ataxia,
depression, hallucinations, syncope, coma; polyuria, polydypsia, nocturia,
hypercalciuria, irreversible renal insufficiency or proteinuria, azotemia; will
spread tissue calcifications, hypertension
Following withdrawal of the drug, treatment consists of bed rest, liberal
intake of fluids, reduced calcium intake, and cathartic administration. Severe
hypercalcemia requires I.V. hydration and forced diuresis. Urine output should
be monitored and maintained at >3 mL/kg/hour. I.V. saline can quickly and
significantly increase excretion of calcium into the urine. Calcitonin,
cholestyramine, prednisone, sodium EDTA and mithramycin have all been used
successfully to treat the more resistant cases of vitamin D-induced
hypercalcemia. |
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Drug
Interactions |
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Decreased effect/levels of vitamin D: Cholestyramine, colestipol, mineral
oil; phenytoin and phenobarbital may inhibit activation and decrease
effectiveness
Increased toxicity: Thiazide diuretics increase calcium |
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Stability |
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Protect from light |
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Mechanism of
Action |
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Synthetic analogue of vitamin D with a faster onset of action; stimulates
calcium and phosphate absorption from the small intestine, promotes secretion of
calcium from bone to blood; promotes renal tubule resorption of
phosphate |
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Pharmacodynamics/Kinetics |
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Peak hypercalcemic effect: Within 2-4 weeks
Duration: Can be as long as 9 weeks
Absorption: Well absorbed from the GI tract
Elimination: In bile and feces; stored in liver, fat, skin, muscle, and bone
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Usual Dosage |
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Oral:
Infants and young Children: Initial: 1-5 mg/day for 4 days, then 0.1-0.5
mg/day
Older Children and Adults: Initial: 0.8-2.4 mg/day for several days followed
by maintenance doses of 0.2-1 mg/day
Nutritional rickets: 0.5 mg as a single dose or 13-50 mcg/day until healing
occurs
Renal osteodystrophy: Maintenance: 0.25-0.6 mg/24 hours adjusted as necessary
to achieve normal serum calcium levels and promote bone healing
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Monitoring
Parameters |
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Monitor renal function, serum calcium, and phosphate concentrations; if
hypercalcemia is encountered, discontinue agent until serum calcium returns to
normal |
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Reference Range |
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Calcium (serum): 9-10 mg/dL (4.5-5 mEq/L) |
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Mental Health: Effects
on Mental Status |
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None reported |
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Mental Health:
Effects on Psychiatric
Treatment |
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Concurrent use with phenytoin or phenobarbital may decrease
effectiveness |
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Dental Health: Local
Anesthetic/Vasoconstrictor
Precautions |
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No information available to require special precautions |
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Dental Health:
Effects on Dental Treatment |
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No effects or complications reported |
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Patient
Information |
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Take exact dose prescribed; do not take more than recommended. Your
prescriber may recommend a special diet. Do not increase calcium intake without
consulting prescriber. Avoid magnesium supplements or magnesium-containing
antacids. You may experience nausea, vomiting, or metallic taste (frequent small
meals, frequent mouth care, or sucking hard candy may help); hypotension (use
caution when rising from sitting or lying position or when climbing stairs or
bending over). Report chest pain or palpitations; acute headache, dizziness, or
feeling of weakness; unresolved nausea or vomiting; persistent metallic taste;
unrelieved muscle or bone pain; or CNS irritability. |
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Nursing
Implications |
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Monitor symptoms of hypercalcemia (weakness, fatigue, somnolence, headache,
anorexia, dry mouth, metallic taste, nausea, vomiting, cramps, diarrhea, muscle
pain, bone pain, and irritability) |
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Dosage Forms |
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Capsule (Hytakerol®): 0.125 mg
Solution:
Oral Concentrate (DHT™): 0.2 mg/mL (30 mL)
Oral, in oil (Hytakerol®): 0.25 mg/mL (15 mL)
Tablet (DHT™): 0.125 mg, 0.2 mg, 0.4 mg
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References |
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Letsou AP and Price LS, "Health Aging and Nutrition: An Overview," Clin
Geriatr Med, 1987, 3(2):253-60.
Myrianthopoulos M, "Dietary Treatment of Hyperlipidemia in the Elderly,"
Clin Geriatr Med, 1987, 3(2):343-59.
Riggs BL and Melton LJ, "The Prevention and Treatment of Osteoporosis," N
Engl J Med, 1992, 327(9):620-7.
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