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Clemastine (Monograph)

Brand names: Dayhist, Tavist
Drug class: First Generation Antihistamines

Medically reviewed by Drugs.com on Jan 22, 2024. Written by ASHP.

Introduction

First generation antihistamine; an ethanolamine derivative.101 102 103 a b

Uses for Clemastine

Allergic Rhinitis

Symptomatic relief of rhinorrhea, sneezing, lacrimation, itching eyes, or oronasopharyngeal itching associated with allergic rhinitis (e.g., hay fever) or other upper respiratory allergies.101 102 103 104 105 a

Allergic Skin Disorders

Management of mild, uncomplicated allergic skin manifestations of urticaria and angioedema.101 102 103 a

Common Cold

Self-medication for temporary relief of symptoms associated with the common cold (e.g., rhinorrhea, sneezing).105 a

Clemastine Dosage and Administration

Administration

Oral Administration

Administer orally as tablets or oral solution.101 102 103 a

Dosage

Available as clemastine fumarate; dosage expressed in terms of the salt.101 102 103 104

1.34 mg clemastine fumarate equivalent to 1 mg clemastine.101 103 104 105 a

Individualize dosage according to patient’s response and tolerance.101 102 103 a b

Pediatric Patients

Allergic Conditions
Allergic Rhinitis
Oral

Children 6 to <12 years of age: Initially, 0.67 mg twice daily (as oral solution).101 103 a Because single doses of up to 3.02 mg have been well tolerated, may increase dosage as necessary, not to exceed 4.02 mg daily.101 103 a

Children ≥12 years of age: 1.34 mg every 12 hours (as tablets or oral solution); this is the maximum dosage recommended for self-medication.104 105 a When used under the direction of a clinician, may increase dosage as necessary, not to exceed 8.04 mg daily.101 102 103 a

Allergic Skin Disorders
Oral

Children 6 to <12 years of age: Initially, 1.34 mg twice daily (as oral solution).101 May increase dosage as necessary, not to exceed 4.02 mg daily.101 103 a

Children ≥12 years of age: 2.68 mg 1–3 times daily (as tablets or oral solution), not to exceed 8.04 mg daily.101 102 103 a

Common Cold
Oral

Self-medication in children ≥12 years of age: Usually, 1.34 mg every 12 hours (as tablets), not to exceed 2.68 mg daily unless otherwise directed by a clinician.a

Adults

Allergic Conditions
Allergic Rhinitis
Oral

Initially, 1.34 mg every 12 hours (as tablets or oral solution); this is the maximum dosage recommended for self-medication.a When used under the direction of a clinician, may increase dosage as necessary, not to exceed 8.04 mg daily.101 102 103 a

Allergic Skin Disorders
Oral

2.68 mg 1–3 times daily (as tablets or oral solution), not to exceed 8.04 mg daily.101 102 103 a

Common Cold
Oral

Self-medication: Usually, 1.34 mg every 12 hours (as tablets), not to exceed 2.68 mg daily unless otherwise directed by a clinician.a

Prescribing Limits

Pediatric Patients

Allergic Conditions
Allergic Rhinitis
Oral

Children 6 to <12 years of age: Maximum 4.02 mg daily.101 a

Children ≥12 years of age: For self-medication, maximum 1.34 mg every 12 hours.a When used under the direction of a clinician, maximum 8.04 mg daily.101 102 a

Allergic Skin Disorders
Oral

Children 6 to <12 years of age: Maximum 4.02 mg daily.101 a

Children ≥12 years of age: Maximum 8.04 mg daily.101 102 a

Common Cold
Oral

Children ≥12 years of age: For self-medication, maximum 2.68 mg daily unless otherwise directed by a clinician.a

Adults

Allergic Conditions
Allergic Rhinitis
Oral

Self-medication: Maximum 1.34 mg every 12 hours.a When used under the direction of a clinician, maximum 8.04 mg daily.101 102 a

Allergic Skin Disorders
Oral

Maximum 8.04 mg daily.101 102 a

Common Cold
Oral

Self-medication: Maximum 2.68 mg daily unless otherwise directed by a clinician.a

Special Populations

Geriatric Patients

Reduce dosage if mild adverse effects occur.b (See Geriatric Use under Cautions.)

Cautions for Clemastine

Contraindications

Warnings/Precautions

Warnings

Concomitant Diseases

Because of anticholinergic effects, use with extreme caution in patients with angle-closure glaucoma, stenosing peptic ulcer, pyloroduodenal obstruction, bladder neck obstruction, or symptomatic prostatic hypertrophy.101 102 103 b

Use with caution in patients with history of bronchial asthma, increased IOP, hyperthyroidism, or cardiovascular disease (e.g., hypertension).101 102 103

CNS Effects

Risk of drowsiness.101 103 b (See CNS Depressants under Interactions and also see Advice to Patients.)

Possible excitability (especially in children).104 105 b (See Pediatric Use under Cautions.)

Specific Populations

Pregnancy

Category B.101 103 106

Lactation

Distributed into milk.c Some manufacturers recommend discontinuance of nursing or the drug because of potential risk to nursing infants (see Contraindications under Cautions).101 102 103 s However, AAP states that the drug may be used with caution during breast-feeding.106

Pediatric Use

Contraindicated in neonates and premature infants.101 103 a

Possible paradoxical excitement (e.g., restlessness, insomnia, tremors, euphoria, nervousness, delirium, palpitation, seizures), especially in children.104 105 b

Safety and efficacy of tablets not established in children <12 years of age.102 a Safety and efficacy of oral solution not established in children <6 years of age.101 103 a

Risk of overdosage and toxicity (including death) in children <2 years of age receiving OTC preparations containing antihistamines, cough suppressants, expectorants, and nasal decongestants alone or in combination for relief of symptoms of upper respiratory tract infection.d v Limited evidence of efficacy for these preparations in this age group; appropriate dosages not established.d Therefore, FDA recommended not to use such preparations in children <2 years of age;e safety and efficacy in older children under evaluation.g i Because children 2–3 years of age also are at increased risk of overdosage and toxicity, some manufacturers of oral nonprescription cough and cold preparations agreed to voluntarily revise the product labeling to state that such preparations should not be used in children <4 years of age.f g h i FDA recommends that parents and caregivers adhere to dosage instructions and warnings on the product labeling that accompanies the preparation and consult a clinician about any concerns.f g h Clinicians should ask caregivers about use of OTC cough/cold preparations to avoid overdosage.d

Geriatric Use

Possible increased risk of dizziness, sedation, and hypotension in patients ≥60 years of age.101 102 103 (See Geriatric Patients under Dosage and Administration.)

Common Adverse Effects

Sedation,101 102 103 sleepiness,101 102 103 dizziness,101 102 103 disturbed coordination,101 102 103 epigastric distress,101 102 103 thickening of bronchial secretions.101 102 103

Drug Interactions

Specific Drugs and Laboratory Tests

Drug or Test

Interaction

Comments

CNS depressants (e.g., alcohol, hypnotics, sedatives, tranquilizers)

Possible additive CNS depression101 102 103 104 105 b

Avoid concomitant use101 103

MAO inhibitors

MAO inhibitors prolong and intensify anticholinergic effects of antihistamines101 102 103 b

Concomitant use contraindicated102

Test, antigen or histamine

Inhalation-challenge testing with histamine or antigen: Possible suppression of test responsek l m n o p q r

Antigen skin testing: Possible suppression of wheal and flare reactionsk l m n o p q r

Clemastine Pharmacokinetics

Absorption

Bioavailability

Rapidly and almost completely absorbed from the GI tract.101 102 103 a

Peak plasma concentrations achieved within 2–5 hours following oral administration.101 102 103 s t u

Onset

Antihistaminic effect is maximal within 5–7 hours.101 102 103 s

Duration

Antihistaminic effect persists for 10–12 hours and, in some individuals, up to 24 hours.101 102 103 s

Distribution

Extent

Distribution into human body fluids and tissues not fully characterized.c s

Distributed into milk.c

Elimination

Metabolism

Exact metabolic fate not clearly established, but appears to be extensively metabolized.s t u

Elimination Route

Excreted principally in urine as unchanged drug and metabolites.101 102 103 s t

Stability

Storage

Oral

Tablets

Tight, light-resistant containers at 20–25°C.102

Oral Solution

Tight, light-resistant, upright containers103 at 20–25°C.101 103

Actions

Advice to Patients

Preparations

Excipients in commercially available drug preparations may have clinically important effects in some individuals; consult specific product labeling for details.

Please refer to the ASHP Drug Shortages Resource Center for information on shortages of one or more of these preparations.

* available from one or more manufacturer, distributor, and/or repackager by generic (nonproprietary) name

Clemastine Fumarate

Routes

Dosage Forms

Strengths

Brand Names

Manufacturer

Oral

Solution

0.67 mg/5 mL*

Clemastine Fumarate Syrup

Tablets

1.34 mg*

Clemastine Fumarate Tablets

Dayhist Allergy

Major

Tavist Allergy (formerly Tavist-1) (scored)

Novartis

2.68 mg*

Clemastine Fumarate Tablets (scored)

AHFS DI Essentials™. © Copyright 2024, Selected Revisions February 1, 2016. American Society of Health-System Pharmacists, Inc., 4500 East-West Highway, Suite 900, Bethesda, Maryland 20814.

References

101. Teva Pharmaceuticals. Clemastine fumarate syrup prescribing information. Sellersville, PA; 2003 Apr.

102. Teva Pharmaceuticals. Clemastine fumarate tablets prescribing information. Sellersville, PA; 2003 Aug.

103. Major Pharmaceuticals. Clemastine fumarate syrup prescribing information. Livonia, MI; 2001 May.

104. Major Pharmaceuticals. Dayhist Allergy product information. Livonia, MI. From Major Pharmaceuticals website. Accessed 2008 Jan 17. http://major-pharm.com/index.php?NR=consumer

105. Novartis. East Hanover, NJ: Personal communication.

106. Clemastine. In: Briggs GG, Freeman RK, Yaffe SJ. Drugs in pregnancy and lactation. 7th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2005:341-2.

a. AHFS Drug Information 2008. McEvoy GK, ed. Clemastine Fumarate. Bethesda, MD: American Society of Health-System Pharmacists; 2008:14-5.

b. AHFS Drug Information 2008. McEvoy GK, ed. Antihistamines General Statement. Bethesda, MD: American Society of Health-System Pharmacists; 2008:1-8.

c. Kok THHG, Taitz LS, Bennett MJ et al. Drowsiness due to clemastine transmitted in breast milk. Lancet. 1982; 1:914-5. http://www.ncbi.nlm.nih.gov/pubmed/6122135?dopt=AbstractPlus

d. Srinivasan A, Budnitz D, Shehab N et al. Infant deaths associated with cough and cold medications—two states, 2005. MMWR Morb Mortal Wkly Rep. 2007; 56:1-4. http://www.ncbi.nlm.nih.gov/pubmed/17218934?dopt=AbstractPlus

e. Food and Drug Administration. FDA news: FDA releases recommendations regarding use of over-the-counter cough and cold products. Rockville, MD; 2008 Jan 17. From the FDA web site. http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/2008

f. Food and Drug Administration. Over the counter cough and cold medications. Rockville, MD; October 2008. From FDA website. http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm094913.htm

g. Food and Drug Administration. FDA statement: FDA statement following CHPA’s announcement on nonprescription over-the-counter cough and cold medicines in children. 2008 Oct 8. From the FDA website. http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/2008/ucm116964.htm

h. Consumer Healthcare Products Association. Statement from CHPA on the voluntary label updates to oral OTC children’s cough and cold medicines. 2008 Oct 7. http://www.chpa-info.org/10_07_08_pedcc.aspx

i. Heavey S. Don’t use cold drugs in kids under 4: manufacturers. Reuters, 2008 Oct 8. From Reuters website. http://uk.reuters.com/articlePrint?articleId=UKTRE4965S520081008

j. Cook TJ, MacQueen DM, Wittig HJ et al. Degree and duration of skin test suppression and side effects with antihistamines: a double blind controlled study with five antihistamines. J Allergy Clin Immunol. 1973; 51:71-7. http://www.ncbi.nlm.nih.gov/pubmed/4405284?dopt=AbstractPlus

k. Galant SP, Bullock J, Wong D et al. The inhibitory effect of antiallergy drugs on allergen and histamine induced wheal and flare response. J Allergy Clin Immunol. 1973; 51:11-21. http://www.ncbi.nlm.nih.gov/pubmed/4118408?dopt=AbstractPlus

l. Chipps BE, Talamo RC, Mellits ED et al. Immediate (IgE-mediated) skin testing in the diagnosis of allergic disease. Ann Allergy. 1978; 41:211-5. http://www.ncbi.nlm.nih.gov/pubmed/81630?dopt=AbstractPlus

m. Galant SP, Zippin C, Bullock J et al. Allergy skin test: I. Antihistamine inhibition. Ann Allergy. 1972; 30:53-63. http://www.ncbi.nlm.nih.gov/pubmed/4400814?dopt=AbstractPlus

n. Diamond GA, Dilibero RJ. Pharmacologic modification of the immediate intradermal skin reaction. Ann Allergy. 1966; 24:288-90. http://www.ncbi.nlm.nih.gov/pubmed/5328526?dopt=AbstractPlus

o. Kern GW IV. Letter to the editors. Clin Allergy. 1982; 12:321. http://www.ncbi.nlm.nih.gov/pubmed/6125277?dopt=AbstractPlus

p. Arnaud A, Vervloet D, Ostorero M et al. Effets des anti-histaminiques (H1 et H2) sur différents types de tests cutanés explorant l’allergie a médiation humorale ou cellulaire. (French; with English abstract.) Nouv Presse Med. 1980; 9:2849. Letter.

q. Johnson CE, Weiner JS, Wagner DS et al. Effect of H1- and H2-receptor blockade on the inhibition of immediate cutaneous reactions. Clin Pharm. 1984; 3:60-4. http://www.ncbi.nlm.nih.gov/pubmed/6141860?dopt=AbstractPlus

r. Smith JA, Mansfield LE, de Shazo RD. An evaluation of the pharmacologic inhibition of the immediate and late cutaneous reaction to allergen. J Allergy Clin Immunol. 1980; 65:118-21.

s. Sandoz Pharmaceuticals Corporation. Tavist (clemastine fumarate) Syrup prescribing information. In: Huff BB, ed. Physicians’ desk reference. 41st ed. Oradell, NJ: Medical Economics Company Inc; 1987:1792-3.

t. Tham R, Norlander B, Hagermark O et al. Gaschromatography of clemastine (a study of plasma kinetics and biological effect). Arzneimittelforschung. 1978; 28:1017-20. http://www.ncbi.nlm.nih.gov/pubmed/35180?dopt=AbstractPlus

u. Paton DM, Webster DR. Clinical pharmacokinetics of H1-receptor antagonists (the antihistamines). Clin Pharmacokinet. 1985; 10:477-97. http://www.ncbi.nlm.nih.gov/pubmed/2866055?dopt=AbstractPlus

v. Food and Drug Administration. Cough and cold medications in children less than two years of age. Rockville, MD; 2007 Jan 12. From FDA website. http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm150441.htm