|
Pronunciation |
|
(deks
troe thye ROKS
een) |
|
|
U.S. Brand
Names |
|
Choloxin® |
|
|
Generic
Available |
|
No |
|
|
Synonyms |
|
Dextrothyroxine Sodium |
|
|
Pharmacological Index |
|
Antilipemic Agent (Miscellaneous) |
|
|
Use |
|
Reduction of elevated serum cholesterol |
|
|
Pregnancy Risk
Factor |
|
C |
|
|
Contraindications |
|
Euthyroid patients with one of the following: Organic heart disease
(including ischemic); congestive heart failure, advanced renal or hepatic
disease, history of myocardial infarction, cardiac arrhythmias, rheumatic heart
disease, hypertension, history of ischism |
|
|
Warnings/Precautions |
|
Use with caution in patients with a history of angina pectoris, severe
hypertension, or myocardial infarction, Do not use for treatment of obesity due
to risk of life-threatening toxicity. Discontinue 2 weeks prior to elective
surgery. Increased serum thyroxine levels are to be expected; do not interpret
as hypermetabolism. |
|
|
Adverse
Reactions |
|
<1% (Limited to important or life-threatening symptoms): Myocardial
infarction, angina, arrhythmias, insomnia, headache, alopecia, rash, weight
loss, tremor, paresthesia, visual disturbances, tinnitus,
diaphoresis |
|
|
Drug
Interactions |
|
Warfarin's effects are increased; avoid concurrent use or decrease warfarin's
dose and monitor INR closely.
Cholestyramine decreases the absorption of dextrothyroxine; separate
administration.
TCAs may increase nervousness, CNS stimulation, tachycardia, and other
arrhythmias.
Beta-blockers may decrease the pharmacologic effects of dextrothyroxine.
Digoxin's efficacy may be reduced with exacerbation of arrhythmias or heart
failure.
Antidiabetic agents may need dose increased to combat hyperglycemia caused by
dextrothyroxine. |
|
|
Mechanism of
Action |
|
Unclear mechanism, thought to increase the liver breakdown of
cholesterol |
|
|
Pharmacodynamics/Kinetics |
|
Absorption: Poorly absorbed from GI tract (25%)
Serum half-life: 18 hours |
|
|
Usual Dosage |
|
Oral:
Adults: 1-2 mg/day, increase at 1-2 mg at intervals of 4 weeks, up to a
maximum of 8 mg/day |
|
|
Dietary
Considerations |
|
Low-fat, low-cholesterol may be recommended |
|
|
Cardiovascular
Considerations |
|
There is no clear benefit for the use of dextrothyroxine in the management of
hyperlipidemia |
|
|
Mental Health: Effects
on Mental Status |
|
May cause insomnia |
|
|
Mental Health:
Effects on Psychiatric
Treatment |
|
Concurrent use with TCAs may increase their toxicity |
|
|
Dental Health: Local
Anesthetic/Vasoconstrictor
Precautions |
|
No information available to require special precautions |
|
|
Dental Health:
Effects on Dental Treatment |
|
No effects or complications reported |
|
|
Patient
Information |
|
If chest pain, palpitations, sweating, diarrhea develop during therapy,
discontinue drug |
|
|
Nursing
Implications |
|
If chest pain, palpitations, sweating, and/or diarrhea develop during
therapy, discontinue drug |
|
|
Dosage Forms |
|
Tablet, as sodium: 2 mg, 4 mg, 6
mg |
|
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