Clemastine (Monograph)
Brand names: Dayhist, Tavist
Drug class: First Generation Antihistamines
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
OralChildren 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
OralChildren 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
OralInitially, 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
Oral2.68 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
OralChildren 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
OralChildren 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
OralSelf-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
OralMaximum 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
-
Use contraindicated in neonates and premature infants.101 103 a (See Pediatric Use under Cautions.)
-
Women who are breast-feeding.101 102 103 (See Lactation under Cautions.)
-
Patients receiving MAO inhibitor therapy.102 (See Interactions.)
-
Known hypersensitivity to clemastine, other antihistamines with similar chemical structure, or any ingredient in the formulation.101 102 103
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
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) |
||
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
-
Blocks H1-receptor sites, thereby preventing the action of histamine on the cell.101 103 b
-
Suppresses flare and pruritus that accompany the endogenous release of histamine.101 b
-
Antihistamines do not block the stimulating effect of histamine on gastric acid secretion, which is mediated by H2-receptors of the parietal cells.b
Advice to Patients
-
Risk of drowsiness; avoid alcohol and avoid engaging in hazardous tasks (e.g., operating machinery, driving a motor vehicle) until effects on individual are known.101 102 103 104 105
-
Importance of informing clinicians of existing or contemplated concomitant therapy, including prescription and OTC drugs and dietary or herbal supplements, as well as any concomitant illnesses.101 102 103 Importance of patients already receiving another CNS depressant (e.g., sedative, tranquilizer) not undertaking self-medication without first consulting a clinician.104
-
Importance of women informing clinicians if they are or plan to become pregnant or plan to breast-feed.101 102 103
-
Importance of informing patients of other important precautionary information.101 102 103 (See Cautions.)
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
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 2025, 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. https://pubmed.ncbi.nlm.nih.gov/6122135
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. https://pubmed.ncbi.nlm.nih.gov/17218934
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. https://pubmed.ncbi.nlm.nih.gov/4405284
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. https://pubmed.ncbi.nlm.nih.gov/4118408
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. https://pubmed.ncbi.nlm.nih.gov/81630
m. Galant SP, Zippin C, Bullock J et al. Allergy skin test: I. Antihistamine inhibition. Ann Allergy. 1972; 30:53-63. https://pubmed.ncbi.nlm.nih.gov/4400814
n. Diamond GA, Dilibero RJ. Pharmacologic modification of the immediate intradermal skin reaction. Ann Allergy. 1966; 24:288-90. https://pubmed.ncbi.nlm.nih.gov/5328526
o. Kern GW IV. Letter to the editors. Clin Allergy. 1982; 12:321. https://pubmed.ncbi.nlm.nih.gov/6125277
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. https://pubmed.ncbi.nlm.nih.gov/6141860
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. https://pubmed.ncbi.nlm.nih.gov/35180
u. Paton DM, Webster DR. Clinical pharmacokinetics of H1-receptor antagonists (the antihistamines). Clin Pharmacokinet. 1985; 10:477-97. https://pubmed.ncbi.nlm.nih.gov/2866055
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
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