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Pronunciation |
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(KLEM
as
teen) |
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U.S. Brand
Names |
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Antihist-1®[OTC]; Tavist®;
Tavist®-1
[OTC] |
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Generic
Available |
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No |
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Synonyms |
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Clemastine Fumarate |
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Pharmacological Index |
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Antihistamine |
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Use |
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Perennial and seasonal allergic rhinitis and other allergic symptoms
including urticaria |
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Pregnancy Risk
Factor |
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C |
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Contraindications |
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Narrow-angle glaucoma, hypersensitivity to clemastine or any
component |
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Warnings/Precautions |
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Safety and efficacy have not been established in children <6 years of age;
bladder neck obstruction, symptomatic prostate hypertrophy, asthmatic attacks,
and stenosing peptic ulcer |
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Adverse
Reactions |
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>10%:
Central nervous system: Slight to moderate drowsiness
Respiratory: Thickening of bronchial secretions
1% to 10%:
Central nervous system: Headache, fatigue, nervousness, increased dizziness
Gastrointestinal: Appetite increase, weight gain, nausea, diarrhea, abdominal
pain, xerostomia
Neuromuscular & skeletal: Arthralgia
Respiratory: Pharyngitis
<1%: Edema, palpitations, depression, angioedema, photosensitivity, rash,
hepatitis, myalgia, paresthesia, bronchospasm, epistaxis |
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Overdosage/Toxicology |
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Symptoms of overdose include anemia, metabolic acidosis, hypotension,
hypothermia
There is no specific treatment for an antihistamine overdose, however, most
of its clinical toxicity is due to anticholinergic effects. For anticholinergic
overdose with severe life-threatening symptoms, physostigmine 1-2 mg (0.5 mg or
0.02 mg/kg for children) I.V., slowly may be given to reverse these effects.
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Drug
Interactions |
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Increased toxicity (CNS depression): CNS depressants, MAO inhibitors,
tricyclic antidepressants, phenothiazines |
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Mechanism of
Action |
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Competes with histamine for H1-receptor sites on effector cells in
the gastrointestinal tract, blood vessels, and respiratory
tract |
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Pharmacodynamics/Kinetics |
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Duration: 8-16 hours
Peak therapeutic effect: Within 5-7 hours
Absorption: Almost 100% from GI tract
Metabolism: In the liver
Elimination: In urine |
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Usual Dosage |
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Oral:
Children >12 years and Adults: 1.34 mg twice daily to 2.68 mg 3 times/day;
do not exceed 8.04 mg/day; lower doses should be considered in patients >60
years |
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Dietary
Considerations |
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Alcohol: Additive CNS effects, avoid use |
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Monitoring
Parameters |
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Look for a reduction of rhinitis, urticaria, eczema, pruritus, or other
allergic symptoms |
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Mental Health: Effects
on Mental Status |
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Drowsiness is common; may cause nervousness; rare reports of
depression |
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Mental Health:
Effects on Psychiatric
Treatment |
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Concurrent use with psychotropics may result in additive
sedation |
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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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Avoid alcohol; may cause drowsiness, may impair coordination or
judgment |
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Nursing
Implications |
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Raise bed rails, institute safety measures, assist with
ambulation |
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Dosage Forms |
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Syrup, as fumarate (citrus flavor): 0.67 mg/5 mL with alcohol 5.5% (120 mL)
Tablet, as fumarate: 1.34 mg, 2.68 mg |
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References |
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Copyright © 1978-2000 Lexi-Comp Inc. All Rights Reserved
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