Fexofenadine

From Wikipedia, the free encyclopedia
  (Redirected from Telfast)
Jump to: navigation, search
Fexofenadine
Fexofenadine2DCSD.svg
Systematic (IUPAC) name
(±)-4-[1 hydroxy-4-[4-(hydroxydiphenylmethyl)-1-piperidinyl]-butyl]-α, α-dimethyl benzeneacetic acid
Clinical data
Trade names Allegra, Axodin
AHFS/Drugs.com monograph
MedlinePlus a697035
Licence data US FDA:link
Pregnancy cat.
Legal status
Routes Oral
Pharmacokinetic data
Bioavailability 30-41%[1]
Protein binding 60-70%[2]
Metabolism Hepatic (≤5% of dose)[2]
Half-life 14.4 hours
Excretion Feces (~80%) and urine (~10%) as unchanged drug[2]
Identifiers
CAS number 83799-24-0 YesY
ATC code R06AX26
PubChem CID 3348
DrugBank DB00950
ChemSpider 3231 YesY
UNII E6582LOH6V YesY
KEGG D07958 YesY
ChEBI CHEBI:5050 YesY
ChEMBL CHEMBL914 YesY
Chemical data
Formula C32H39NO4 
Mol. mass 501.68
 N (what is this?)  (verify)

Fexofenadine (trade names Allegra, Fexidine, Telfast, Fastofen, Tilfur, Vifas, Telfexo, Allerfexo) is an antihistamine pharmaceutical drug used in the treatment of allergy symptoms, such as hay fever, nasal congestion, and urticaria.[3] It is often said to be a third-generation antihistamine, which means that its effect are limited to the periphery, that is, outside the brain and spinal cord, which is where most antihistamines mediate their sedating effects, hence fexofenadine produces minimal sedation.[4]

Medical uses[edit]

Fexofenadine is used for relief from physical symptoms associated with seasonal allergic rhinitis and for treatment of chronic urticaria.[4] It does not cure but rather prevents the aggravation of rhinitis and urticaria and reduces the severity of the symptoms associated with those conditions, providing relief from repeated sneezing, runny nose, itchy eyes and general body fatigue.

Dosage[edit]

Fexofenadine has been demonstrated to be safe and effective for children ages 2–5 years old and 6–11 years old in treatment of seasonal allergic rhinitis.[5][6]

  • Renal Impairment: Due to decreased renal elimination in patients with creatinine clearance of less than 80mL/min, it is recommended that patients with renal impairment are started on a lower dose.[7]
  • Hepatic Impairment: Perhaps because only a small percentage of fexofenadine is metabolized in the liver, altered levels of drug are not seen in patients with hepatic impairment and therefore doses do not need to be adjusted in this population.[7]

Side effects[edit]

The most common side effects demonstrated in adults were headache, back pain, miosis or pinpoint pupils, drowsiness, and menstrual cramps. There have also been reports of anxiety and insomnia. The most common side effects demonstrated during clinical trials were cough, upper respiratory tract infection, fever, and otitis media for children ages 6 to 11 and fatigue for children ages 6 months to 5 years.[7]

Additionally, the half-life of fexofenadine is shorter than cetirizine, so it often must be taken twice daily.[8] However, there is also evidence that cetirizine causes more sleepiness than fexofenadine.[9]

Overdose[edit]

The safety profile of fexofenadine is quite favorable, as no cardiovascular or sedative effects have been shown to occur even when taking 10 times the recommended dose.[10] Research on humans ranges from a single 800 mg dose, to a twice-daily 690 mg dose for a month, with no clinically significant adverse effects, when compared to a placebo. No deaths occurred in testing on mice, at 5000 mg/kg body weight, which is one-hundred and ten times (110x) the maximum recommended dose for an adult human.[7] If overdose were to occur, likely seen as dizziness, dry mouth, and/or drowsiness, supportive measures are recommended. It does not appear that hemodialysis is an effective mode to remove fexofenadine from the blood.[7]

Mechanism of action[edit]

Fexofenadine is a second-generation selectively peripheral H1-blocker. Blockage prevents the activation of the H1 receptors by histamine, preventing the symptoms associated with allergies from occurring. Fexofenadine does not readily cross the blood–brain barrier and is therefore unlikely to cause drowsiness. It also exhibits no anticholinergic, antidopaminergic, alpha1-adrenergic, or beta-adrenergic-receptor-blocking effects.[7]

Pharmacokinetics[edit]

Absorption: After oral application, maximum plasma concentrations are reached after two to three hours. Fexofenadine should not be taken with a high fat meal, as mean concentrations of fexofenadine in the bloodstream is seen to be reduced from 20-60% depending on form of medication (tablet, ODT, or suspension).[7]

Distribution: Fexofenadine is 60-70% bound to plasma proteins, mostly albumin.[7]

Metabolism: Only a 5% is metabolized in the liver.[7]

Elimination: Most of the substance is eliminated unchanged via the feces (80%) and urine (11–12%).[7]

Interactions[edit]

Taking erythromycin or ketoconazole while taking fexofenadine does increase the plasma levels of fexofenadine, but this increase does not influence the QT interval. The reason for this effect is likely to do transport-related effects, specifically involving p-glycoprotein.[7]

Fexofenadine is not to be taken with apple, orange, or grapefruit juice because it could decrease absorption of the drug and should therefore be taken with water.[7] Grapefruit juice can significantly reduce the plasma concentration of fexofenadine.[11]

Antacids containing aluminium or magnesium should not be taken within 15 minutes of fexofenadine as they reduce the absorption of fexofenadine by almost 50%.[7]

Special populations[edit]

Fexofenadine is a pregnancy category C and should be used if the benefits outweigh the risks.[12]

No studies have been done to evaluate the presence of fexofenadine in breast milk. Therefore, nursing women are urged to take caution while using fexofenadine.[7]

No sufficient studies have been done in patients over age 65. Therefore, it is advised that elderly patients use caution when using fexofenadine, particularly when there is concern for renal impairment.[7]

History[edit]

The older antihistaminic agent terfenadine was found to metabolize into the related carboxylic acid, fexofenadine. Fexofenadine was found to retain all of the biological activity of its parent while giving fewer adverse reactions in patients, so terfenadine was replaced in the market by its metabolite.[13] Fexofenadine was originally synthesized in 1993 by Massachusetts-based biotechnology company Sepracor, which then sold the development rights to Hoechst Marion Roussel (now part of Sanofi-Aventis), and was later approved by the Food and Drug Administration (FDA) in 1996. Albany Molecular Research Inc. (AMRI) holds the patents to the intermediates and production of fexofenadine HCl along with Roussel. Since that time, it has achieved blockbuster drug status with global sales of $1.87B USD in 2004 (with $1.49B USD coming from the United States). AMRI received royalty payments from Aventis that enabled the growth of AMRI.

On January 25, 2011, the FDA approved over-the-counter sales of fexofenadine in the United States, and Sanofi-Aventis' version became available on March 4, 2011.[14]

See also[edit]

References[edit]

  1. ^ Lappin G, Shishikura Y, Jochemsen R, Weaver RJ, Gesson C, Houston B, Oosterhuis B, Bjerrum OJ, Rowland M, Garner C (May 2010). "Pharmacokinetics of fexofenadine: evaluation of a microdose and assessment of absolute oral bioavailability". Eur J Pharm Sci 40 (2): 125–31. doi:10.1016/j.ejps.2010.03.009. PMID 20307657. 
  2. ^ a b c Smith, SM; Gums, JG (July 2009). "Fexofenadine: biochemical, pharmacokinetic and pharmacodynamic properties and its unique role in allergic disorders.". Expert Opinion on Drug Metabolism & Toxicology 5 (7): 813–22. doi:10.1517/17425250903044967. PMID 19545214. 
  3. ^ Bachert, C (May 2009). "A review of the efficacy of desloratadine, fexofenadine, and levocetirizine in the treatment of nasal congestion in patients with allergic rhinitis". Clin Ther 31 (5): 921–44. doi:10.1016/j.clinthera.2009.05.017. PMID 19539095. Retrieved 18 April 2014. 
  4. ^ a b Compalati, E; Baena-Cagnani, R; Penagos, M; Badellino, H; Braido, F; Gómez, RM; Canonica, GW; Baena-Cagnani, CE (2011). "Systematic review on the efficacy of fexofenadine in seasonal allergic rhinitis: a meta-analysis of randomized, double-blind, placebo-controlled clinical trials.". International Archives of Allergy and Immunology 156 (1): 1–15. doi:10.1159/000321896. PMID 21969990. 
  5. ^ Segall, N; Grubbe RE; Levy AL; Maloney MJ; Nayak AS; Kittner B; Quesada JT. (Jul–Aug 2008). "Pharmacokinetics, Safety and Tolerability of an Oral Suspension of Fexofenadine for Children with Allergic Rhinitis". Allergy Asthma Proc. 29 (4): 380–5. doi:10.2500/aap.2008.29.3136. PMID 18702885. Retrieved 17 April 2014. 
  6. ^ Phan, H; Moeller, Nahata (2009). "Treatment of Allergic Rhinitis in Infants and Children: Efficacy and Safety of Second-Generation Antihistamines and the Leukotriene Receptor Antagonist Montelukast". Drugs 69 (18): 2541–76. doi:10.2165/9884960-000000000-00000. PMID 19943707. Retrieved 17 April 2014. 
  7. ^ a b c d e f g h i j k l m n o Allegra (fexofenadine hydrochloride) tablets, ODT, and oral suspension package insert. Sanofi-Aventis; 2007.
  8. ^ Church, Martin; Church, Diana (2013). "Pharmacology of antihistamines". Indian Journal of Dermatology 58 (3): 219–224. doi:10.1097/WOX.0b013e3181f385d9. PMC 3666185. PMID 23282332. Retrieved 18 April 2014. 
  9. ^ Tashiro, M; Sakurada Y, Iwabuchi K, Mochizuki H, Kato M, Aoki M, Funaki Y, Itoh M, Iwata R, Wong DF, Yanai K (Aug 2004). "Central effects of fexofenadine and cetirizine: measurement of psychomotor performance, subjective sleepiness, and brain histamine H1-receptor occupancy using 11C-doxepin positron emission tomography.". J Clin Pharmacol 44 (8): 890–900. doi:10.1177/0091270004267590. PMID 15286093. Retrieved 18 April 2014. 
  10. ^ Philpot, EE (Jan–Feb 2000). "Safety of second generation antihistamines". Allergy Asthma Proc 21 (1): 15–20. doi:10.2500/108854100778249033. PMID 10748947. 
  11. ^ Shirasaka, Y; Mori T; Murata Y; Nakanishi T; Tamai I (Feb 19, 2014). "Substrate- and Dose-Dependent Drug Interactions with Grapefruit Juice Caused by Multiple Binding Sites on OATP2B1". Pharm Res. doi:10.1007/s11095-014-1305-7. PMID 24549825. 
  12. ^ Mazzotta, P; Loebstein R; Koren G (Apr 1999). "Treating allergic rhinitis in pregnancy. Safety considerations.". Drug Saf. 20 (4): 361–75. doi:10.2165/00002018-199920040-00005. PMID 10230583. Retrieved 18 April 2014. 
  13. ^ Daniel Lednicer (1999). The Organic Chemistry of Drug Synthesis 6. New York: Wiley Interscience. pp. 38–40. ISBN 0-471-24510-0. 
  14. ^ "Allegra | FAQs". Sanofi-Aventis. Retrieved 5 July 2011. 

External links[edit]