Fexofenadine

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Fexofenadine chemical structure
Fexofenadine
Systematic (IUPAC) name
2-[4-[1-hydroxy-4-[4-(hydroxy-diphenyl-

methyl)-1-piperidyl]butyl]phenyl]-2- methyl-propanoic acid

Identifiers
CAS number 83799-24-0
ATC code R06A626
PubChem 3348
DrugBank APRD00349
Chemical data
Formula C32H39NO4
Mol. weight 501.656
Pharmacokinetic data
Bioavailability Not yet established
Protein binding 60-70%
Metabolism Hepatic (5% of dose)
Half life 14.4 hours
Excretion Biliary , fecal and renal
Therapeutic considerations
Pregnancy cat.

C (US)
B2 (Australia)

Legal status

Prescription Only (US, UK)
OTC (Canada, Australia)

Routes Oral

Fexofenadine hydrochloride (brand names include Allegra® and Telfast®) is an antihistamine drug used in the treatment of hayfever and similar allergy symptoms. It was developed as a successor of and alternative to terfenadine, an antihistamine with potentially fatal contraindications. Fexofenadine, like other second-generation antihistamines, does not readily enter the brain from the blood, and so causes less drowsiness than first-generation histamine-receptor antagonists.

Contents

[edit] Common Side Effects

  • Nausea
  • Vomiting
  • Weakness
  • Drowsiness, sleepiness
  • Depression

[edit] Overdose

Reports of Fexofenadine overdose are infrequent, and because of this, the effects are not well established. No deaths occurred in testing on mice, at 5000 mg/kg, which is 110 times the maximum recommended dose for an adult human. Further research shows no deaths in rats at the same concentration, which equates four hundred times the recommended dose in an adult human. 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.

[edit] History

Fexofenadine was developed by Hoechst Marion Roussel (now part of Aventis) and approved by the Food and Drug Administration (FDA) in 1996. 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).

[edit] References

  • Synthesis: J. Org. Chem. 1994, 59, 2620.
  • Biological effects: Mol. Pharmacol. 1993, 44, 1240.

[edit] External links


Antihistamines (primarily R06) edit
Aminoalkyl ethers:

Bromazine, Carbinoxamine, Clemastine, Chlorphenoxamine, Diphenylpyraline, Diphenhydramine, Doxylamine

Substituted alkylamines:

Brompheniramine, Chlorphenamine, Dexbrompheniramine , Dexchlorpheniramine, Dimetindene, Pheniramine, Talastine

Substituted ethylene diamines:

Chloropyramine, Histapyrrodine, Mepyramine, Methapyrilene

Phenothiazine derivatives:

Alimemazine, Hydroxyethylpromethazine, Isothipendyl, Mequitazine, Methdilazine, Oxomemazine, Promethazine

Piperazine derivatives:

Buclizine, Cetirizine, Chlorcyclizine, Cinnarizine, Cyclizine, Hydroxyzine, Levocetirizine, Meclozine, Oxatomide

Others for systemic use:

Acrivastine, Antazoline, Astemizole, Azatadine , Azelastine, Bamipine, Cyproheptadine, Deptropine, Desloratadine, Ebastine, Epinastine, Ketotifen, Loratadine, Mebhydrolin, Mizolastine, Phenindamine, Pimethixene, Pyrrobutamine, Rupatadine, Terfenadine, Triprolidine

For topical use:

Bamipine, Chloropyramine, Chlorphenoxamine, Clemastine, Dimetindene, Diphenhydramine, Isothipendyl, Mepyramine , Promethazine, Thenalidine

Antiallergic agents
excluding corticosteroids
:

Antazoline, Azelastine , Fexofenadine

Other antiallergics:

Emedastine, Epinastine, Ketotifen, Olopatadine


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