Guaifenesin

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Guaifenesin
Guaifenesin.svg
Systematic (IUPAC) name
(RS)-3-(2-methoxyphenoxy)propane-1,2-diol
Clinical data
Trade names Mucinex
AHFS/Drugs.com monograph
MedlinePlus a682494
Licence data US FDA:link
Pregnancy
category
  • US: C (Risk not ruled out)
Legal status
Routes of
administration
Oral
Pharmacokinetic data
Metabolism Renal
Biological half-life 1-5 hours[1]
Identifiers
CAS Number 93-14-1 YesY
ATC code R05CA03 (WHO) QM03BX90 (WHO)
PubChem CID: 3516
IUPHAR/BPS 7617
DrugBank DB00874 YesY
ChemSpider 3396 YesY
UNII 495W7451VQ YesY
KEGG D00337 YesY
ChEMBL CHEMBL980 YesY
Chemical data
Formula C10H14O4
Molecular mass 198.216 g/mol
  • O(c1ccccc1OC)CC(O)CO
  • InChI=1S/C10H14O4/c1-13-9-4-2-3-5-10(9)14-7-8(12)6-11/h2-5,8,11-12H,6-7H2,1H3 YesY
  • Key:HSRJKNPTNIJEKV-UHFFFAOYSA-N YesY
  (verify)

Guaifenesin INN /ɡwˈfɛnsɪn/ or guaiphenesin (former BAN), also glyceryl guaiacolate,[2] is an expectorant drug sold over the counter and usually taken orally to assist the bringing up (expectoration) of phlegm from the airways in acute respiratory tract infections.

History

Similar medicines derived from the guaiac tree were in use as a generic remedy by American indigenous peoples when explorers reached North America in the 16th century. The Spanish encountered guaiacum wood "when they conquered Santo Domingo; it was soon brought back to Europe, where it acquired an immense reputation in the sixteenth century as a cure for syphilis and certain other diseases..."[3]

The 1955 edition of the Textbook of Pharmacognosy states: "Guaiacum has a local stimulant action which is sometimes useful in sore throat. The resin is used in chronic gout and rheumatism, whilst the wood is an ingredient in the compound concentrated solution of sarsaparilla, which was formerly much used as an alternative in syphilis."[3]

Guaifenesin was first approved by the Food and Drug Administration (FDA) in 1952. Although previously deemed "Generally Regarded as Safe" in its original approval, the drug received a New Drug Application for the extended-release version, which won approval on July 12, 2002. Because of this, the FDA then issued letters to other manufacturers of timed-release guaifenesin to stop marketing their unapproved versions, leaving Adams Respiratory Therapeutics in control of the market. Adams was subsequently acquired by Reckitt Benckiser, based on the strength of the marketing generated by Adams' Mucinex brand.[4][5]

Availability

Guaifenesin is sold as pills or syrups under many brand names. Single-ingredient formulations of guaifenesin are available, and it is also included in many other over-the-counter cough and cold remedy combinations (usually in conjunction with dextromethorphan, acetaminophen, ephedrine, pseudoephedrine, or phenylephrine). Guaifenesin is available under countless brand names and formulations, some of which are:

Medical uses

Cough

The principal use of guaifenesin is in the treatment of coughing. A Cochrane Collaboration meta-analysis of over-the-counter medicines for acute cough in children and adults concluded that there was not enough high-quality clinical data to prove or disprove the effectiveness of any examined drug including guaifenesin.[6] Guaifenesin is sometimes combined with dextromethorphan, an antitussive, such as in Mucinex DM or Robitussin DM.[7]

Other uses

The guaifenesin protocol uses guaifenesin as an unapproved fibromyalgia treatment, despite the fact that a one-year double-blind study indicates that the treatment performs no better than placebo.[8][9] Guaifenesin has not been approved by the FDA for the treatment of fibromyalgia.

Based on a small, non-blinded study,[10] guaifenesin has been promoted to facilitate conception, by thinning and increasing cervical mucus, during the few days before ovulation.[11]

Mechanism of action

Guaifenesin is thought to act as an expectorant by increasing the volume and reducing the viscosity of secretions in the trachea and bronchi. It has been said to aid in the flow of respiratory tract secretions, allowing ciliary movement to carry the loosened secretions upward toward the pharynx.[12] Thus, it may increase the efficiency of the cough reflex and facilitate removal of the secretions.

Guaifenesin has muscle relaxant and anticonvulsant properties and may be acting as an NMDA receptor antagonist.[13]

Side-effects

Side-effects of guaifenesin include nausea, vomiting, formation of kidney stones,[14] diarrhea, and constipation.[15] Nausea and vomiting can be reduced by taking guaifenesin with meals.[2] The risk of forming kidney stones during prolonged use can be reduced by maintaining good hydration and increasing the pH of urine. Rarely, severe allergic reactions may occur, including a rash or swelling of the lips or face, which may require urgent medical assistance. Mild dry mouth or chapped lips may also occur when taking this medication. Drinking a glass of water is recommended each time one takes guaifenesin.[16]

Guaifenesin increases the analgesic effect of paracetamol (acetaminophen) and aspirin, increases the sedative effects of alcohol, tranquilisers, sleep-pills and total anesthetics. Guaifenesin increases the effects of medication that decrease muscle tone.[citation needed]

Veterinary use

Guaifenesin's neurological properties first became known in the late 1940s. Guaifenesin is a centrally acting muscle relaxant used routinely in large-animal veterinary surgery. Guaifenesin is used in combination with, for example, propofol, since guaifenesin does not produce analgesia nor does it produce unconsciousness.[17][18]

See also

References

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  12. Gutierrez, K. (2007). Pharmacotherapeutics: Clinical Reasoning in Primary Care. W.B. Saunders Co.
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  15. Guaifenesin Side Effects http://www.drugs.com/sfx/guaifenesin-side-effects.html
  16. Guaifenesin http://www.nlm.nih.gov/medlineplus/druginfo/meds/a682494.html
  17. Tranquilli, W. J., Thurmon, J. C., and Grimm, K. A. 2007. Lumb and Jones’ Veterinary Anesthesia and Analgesia. Blackwell Publishing. Chapter: Centrally Acting Muscle Relaxants.
  18. Lua error in package.lua at line 80: module 'strict' not found.

External links