Amoxicillin
|
|
| Systematic (IUPAC) name |
| (2S,5R,6R)- 6-{[(2R)-2-amino- 2-(4-hydroxyphenyl)- acetyl]amino}- 3,3-dimethyl- 7-oxo- 4-thia- 1-azabicyclo[3.2.0]heptane- 2-carboxylic acid |
| Clinical data |
| Trade names |
Actimoxi, Alphamox, Amocla,Tycil, Amoxil, Trimox, among others |
| AHFS/Drugs.com |
monograph |
| MedlinePlus |
a685001 |
| Pregnancy cat. |
A (AU) B (US) |
| Legal status |
POM (UK) ℞-only (US) |
| Routes |
Oral, intravenous |
| Pharmacokinetic data |
| Bioavailability |
95% oral |
| Metabolism |
less than 30% biotransformed in liver |
| Half-life |
61.3 minutes |
| Excretion |
renal |
| Identifiers |
| CAS number |
26787-78-0 Y |
| ATC code |
J01CA04 QG51AA03 |
| PubChem |
CID 33613 |
| DrugBank |
DB01060 |
| ChemSpider |
31006 Y |
| UNII |
9EM05410Q9 Y |
| KEGG |
D07452 Y |
| ChEBI |
CHEBI:2676 Y |
| ChEMBL |
CHEMBL1082 Y |
| Chemical data |
| Formula |
C16H19N3O5S |
| Mol. mass |
365.4 g/mol |
SMILES
- O=C(O)[C@@H]2N3C(=O)[C@@H](NC(=O)[C@@H](c1ccc(O)cc1)N)[C@H]3SC2(C)C
|
InChI
-
InChI=1S/C16H19N3O5S/c1-16(2)11(15(23)24)19-13(22)10(14(19)25-16)18-12(21)9(17)7-3-5-8(20)6-4-7/h3-6,9-11,14,20H,17H2,1-2H3,(H,18,21)(H,23,24)/t9-,10-,11+,14-/m1/s1 Y
Key:LSQZJLSUYDQPKJ-NJBDSQKTSA-N Y
|
Y (what is this?) (verify)
|
Amoxicillin (INN), formerly amoxycillin (BAN) in some markets, and abbreviated amox, is a moderate-spectrum, bacteriolytic, β-lactam antibiotic used to treat bacterial infections caused by susceptible microorganisms. It is usually the drug of choice within the class because it is better absorbed, following oral administration, than other β-lactam antibiotics. Amoxicillin is one of the most common antibiotics prescribed for children.
Amoxicillin is susceptible to degradation by β-lactamase-producing bacteria, which are resistant to a broad spectrum of β-lactam antibiotics, such as penicillin. For this reason, it is often combined with clavulanic acid, a β-lactamase inhibitor. This increases effectiveness by reducing its susceptibility to β-lactamase resistance.
|
Contents
- 1 Medical uses
- 2 Adverse effects
- 2.1 Nonallergic amoxicillin rash
- 2.2 Interaction
- 3 Mechanism of action
- 4 Spectrum of Bacterial Susceptibility and Resistance
- 5 Formulations
- 5.1 Modes of delivery
- 5.2 Proprietary preparations
- 6 References
- 7 Further reading
- 8 External links
|
Medical uses
Amoxicillin is used in the treatment of a number of infections including: acute otitis media, streptococcal pharyngitis, pneumonia, skin infections, urinary tract infections, salmonella, lyme disease, and chlamydia infections.[1] It is also used to prevent bacterial endocarditis in high risk people who are having dental work done, to prevent strep pneumococus infections in those without a spleen, and for both the prevention and the treatment of anthrax.[1] The UK however does not recommend its use for infectious endocarditis prophylaxis.[2] These recommendations have not appeared to have changed the rates of infection.[3]
Amoxicillin or amoxicillin-clavulanate are recommended by guidelines as the first-choice drug for bacterial sinusitis. However, most sinusitis is caused by viruses, for which it is ineffective.[4][5] Amoxicillin is occasionally used for the treatment of skin infections, such as acne vulgaris.[6] Amoxicillin is often an effective treatment for cases of acne vulgaris that have responded poorly to other antibiotics, like doxycycline and minocycline.[7]
Adverse effects
Side-effects are as those for other beta-lactam antibiotics. Side-effects include nausea, vomiting, rashes, and antibiotic-associated colitis. Loose bowel movements (diarrhea) may also occur. Rarer side-effects include mental changes, lightheadedness, insomnia, confusion, anxiety, sensitivity to lights and sounds, and unclear thinking. Immediate medical care is required upon the first signs of these side-effects.
The onset of an allergic reaction to amoxicillin can be very sudden and intense - emergency medical attention must be sought as quickly as possible. The initial onset of such a reaction often starts with a change in mental state, skin rash with intense itching (often beginning in fingertips and around groin area and rapidly spreading), and sensations of fever, nausea, and vomiting. Any other symptoms that seem even remotely suspicious must be taken very seriously. However, more mild allergy symptoms, such as a rash, can occur at any time during treatment, even up to a week after treatment has ceased. For some people who are allergic to amoxicillin the side-effects can be deadly.
Use of the amoxicillin/clavulanic acid combination for more than one week has caused mild hepatitis in some patients. Young children having ingested acute overdoses of amoxicillin manifested lethargy, vomiting and renal dysfunction.[8][9]
Nonallergic amoxicillin rash
Somewhere between 3% and 10% of children taking amoxicillin (or ampicillin) show a late-developing (>72 hours after beginning medication and having never taken penicillin-like medication previously) rash, which is sometimes referred to as the "amoxicillin rash." The rash can also occur in adults.
The rash is described as maculopapular or morbilliform (measles-like; therefore, in medical literature, it is called "amoxicillin-induced morbilliform rash"[10]). It starts on the trunk and can spread from there. This rash is unlikely to be a true allergic reaction, and is not a contraindication for future amoxicillin usage, nor should the current regimen necessarily be stopped. However, this common amoxicillin rash and a dangerous allergic reaction cannot easily be distinguished by inexperienced persons, and therefore a healthcare professional is often required to distinguish between the two.[11]
A nonallergic amoxicillin rash may also be an indicator of infectious mononucleosis: Some studies indicate approximately 80-90% of patients with acute Epstein Barr virus infection treated with amoxicillin or ampicillin develop such a rash.[12]
-
Nonallergic amoxicillin rash 8 days after first dose, 24 hours after rash began. Diagnosed by a pediatric resident at local university hospital.
-
Eight hours after first photo, individual spots have grown and begun to merge.
-
Twenty-three hours after first photo, the color appears to be fading, and much of rash has spread to confluence.
Interaction
Amoxicillin may interact with the following groups of drugs:
- Anticoagulants (e.g. warfarin, pradaxa)[13]
- Allopurinol (gout treatment)
- Birth control pills[citation needed]
- Certain antibiotics
- Cancer treatment (methotrexate)
- Uricosuric drugs
- Typhoid vaccine
Mechanism of action
Main article: Beta-lactam antibiotic
This drug acts by inhibiting the synthesis of bacterial cell walls. It inhibits cross-linkage between the linear peptidoglycan polymer chains that make up a major component of the cell walls of both Gram-positive and Gram-negative bacteria.
It has two ionizable groups in the physiological range (the amino group in alpha-position to the amide carbonyl group and the carboxyl group).
Spectrum of Bacterial Susceptibility and Resistance
Bacillus subtilis, Enterococcus, Haemophilus, Helicobacter and Moraxella species are generally susceptible to amoxicillin, while Citrobacter, Klebsiella and Pseudomonas aeruginosa are resistant to amoxicillin.[14] Some E. coli and Staphylococcus aureus have developed resistance to amoxicillin to varying degrees.
Formulations
Modes of delivery
Pharmaceutical manufacturers make amoxicillin in trihydrate form available as capsules, chewable and dispersible tablets plus syrup and pediatric suspension for oral use, and as the sodium salt for intravenous administration (although the IV formulation is not available in the United States[15]).
Amoxicillin is most commonly taken orally. The liquid forms are helpful where the patient might find it difficult to take tablets or capsules.
Research with mice (published in 2010) indicates successful delivery using intraperitoneally injected amoxicillin-bearing microparticles.[16]
Proprietary preparations
|
|
This section does not cite any references or sources. Please help improve this section by adding citations to reliable sources. Unsourced material may be challenged and removed. (February 2010) |
Novamoxin Prescription Drug - 500mg Amoxicillin Trihydrate
Amoxicillin is one of the semisynthetic penicillins discovered by Beecham scientists. The patent for amoxicillin has expired, thus amoxicillin is marketed under many trade names, including:
- Actimoxi
- Alphamox
- Amimox
- Amocla
- AMK
- Amoksibos
- Amoxiclav Sandoz
- Amoxidal
- Amoxil
- Amoxin
- Amoksiklav (with clavulanic acid)
- Amoxibiotic
- Amoxicilina
- Amoxidal
- Apo-Amoxi
- Arsogil
- Augmentin (with clavulanic acid)
|
- Bactox
- Betalaktam
- Bioxidona
- Cilamox
- Clamoxyl
- Clonamox
- Curam
- Dedoxil
- Dispermox
- Duomox
- Defender 625 mg (with clavulanic acid)
- E-Mox
- Enhancin
- Ezymox 500 mg
- Ezymox-DC (Dicloxacin)
- Gimalxina
- Geramox
- Hiconcil
- Isimoxin
- Klavax
|
- Klavocin
- Klavox
- Lamoxy
- Largopen
- Moxatag
- Moxilen
- Moxypen
- Moxyvit
- Nobactam
- Novamoxin
- Ospamox
- Panklav (with clavulanic acid)
- Optamox
- Pamoxicillin
- Panamox
- Polymox
|
- Polymoxyl (PPM Product, Cambodia)
- Samthongcillin
- Senox
- Sinacilin
- Spektramox (with clavulanic acid)
- Starmox
- Trimox
- Tolodina
- Tormoxin
- Unimox
- Wedemox
- Wymox
- Yucla
- Zerrsox
- Zimox
- Zoxicillin (Zafa)
|
References
- ^ a b "Amoxicillin". The American Society of Health-System Pharmacists. http://www.drugs.com/monograph/amoxicillin.html. Retrieved 3 April 2011.
- ^ "CG64 Prophylaxis against infective endocarditis: Full guidance". NICE. http://www.nice.org.uk/nicemedia/live/11938/40039/40039.pdf. Retrieved 8 June 2011.
- ^ Thornhill, MH; Dayer, MJ, Forde, JM, Corey, GR, Chu, VH, Couper, DJ, Lockhart, PB (2011-05-03). "Impact of the NICE guideline recommending cessation of antibiotic prophylaxis for prevention of infective endocarditis: before and after study". BMJ (Clinical research ed.) 342: d2392. doi:10.1136/bmj.d2392. PMC 3086390. PMID 21540258. //www.ncbi.nlm.nih.gov/pmc/articles/PMC3086390/.
- ^ American Academy of Allergy, Asthma, and Immunology. "Five Things Physicians and Patients Should Question". Choosing Wisely: an initiative of the ABIM Foundation (American Academy of Allergy, Asthma, and Immunology). http://choosingwisely.org/wp-content/uploads/2012/04/5things_12_factsheet_AAAAI.pdf. Retrieved August 14, 2012.
- ^ Ahovuo-Saloranta, A.; Rautakorpi, U. M.; Borisenko, O. V.; Liira, H.; Williams Jr, J. W.; Mäkelä, M. (2008). "Antibiotics for acute maxillary sinusitis". In Ahovuo-Saloranta, Anneli. Cochrane Database of Systematic Reviews. doi:10.1002/14651858.CD000243.pub2. edit
- ^ "Adolescent Acne: Management". http://www.medscape.com/viewarticle/430534_5.
- ^ "Amoxicillin and Acne Vulgaris". scienceofacne.com. 2012-09-05. http://scienceofacne.com/amoxicillin/. Retrieved 2012-08-17.
- ^ Cundiff J, Joe S. Amoxicillin-clavulanic acid-induced hepatitis. Amer. J. Otolaryngol. 28: 28-30, 2007.
- ^ R. Baselt, Disposition of Toxic Drugs and Chemicals in Man, 8th edition, Biomedical Publications, Foster City, CA, 2008, pp. 81-83.
- ^ "Role of delayed cellular hypersensitivity and adhesion molecules in amoxicillin-induced morbilliform rashes". Cat.inist.fr. http://cat.inist.fr/?aModele=afficheN&cpsidt=2654598. Retrieved 2010-11-13.
- ^ (Pichichero, 2005; Schmitt 2005)
- ^ Kagan, B (1977). "Ampicillin rash". Western Journal of Medicine 126 (4): 333–335. PMC 1237570. PMID 855325. //www.ncbi.nlm.nih.gov/pmc/articles/PMC1237570/.
- ^ British National Formulary 57 March 2009
- ^ "Amoxicillin spectrum of bacterial susceptibility and Resistance". http://www.toku-e.com/Upload/Products/PDS/20120604005406.pdf. Retrieved 8 April 2012.
- ^ www.UpToDate.com
- ^ Amoxicillin bearing microparticles: potential in treatment of Listeria monocytogenes infection in Swiss albino mice, Bioscience reports immediate publication, 2010-08-05, manuscript BSR 20100027
Further reading
- Neal, M. J. (2002). Medical pharmacology at a glance (4th ed.). Oxford: Blackwell Science. ISBN 0-632-05244-9.
- Pichichero ME (April 2005). "A review of evidence supporting the American Academy of Pediatrics recommendation for prescribing cephalosporin antibiotics for penicillin-allergic patients". Pediatrics 115 (4): 1048–57. doi:10.1542/peds.2004-1276. PMID 15805383. http://pediatrics.aappublications.org/cgi/content/full/115/4/1048.
- Schmitt, Barton D. (2005). Your child's health: the parents' one-stop reference guide to symptoms, emergencies, common illnesses, behavior problems, healthy development (2nd ed.). New York: Bantam Books. ISBN 0-553-38369-8.
- British National Formulary 45 March 2003
External links
- University of Michigan Mott's Children's Hospital article about "amoxicillin rash."[dead link] (Very similar to Schmitt 2005 content)[dead link]
- U.S. National Library of Medicine: Drug Information Portal - Amoxicillin
|
Antibacterials: cell envelope antibiotics (J01C-J01D)
|
|
| Intracellular |
- inhibit peptidoglycan subunit synthesis and transport: NAM synthesis inhibition (Fosfomycin)
- DADAL/AR inhibitors (Cycloserine)
- bactoprenol inhibitors (Bacitracin)
|
|
| Glycopeptide |
- inhibit PG chain elongation: Vancomycin# (Oritavancin
- Telavancin)
- Teicoplanin (Dalbavancin)
- Ramoplanin
|
|
β-lactams/
(inhibit PBP
cross-links) |
|
Penicillins
(penams)
|
|
Extended sp.
|
- aminopenicillins: Amoxicillin#
- Ampicillin# (Pivampicillin
- Hetacillin
- Bacampicillin
- Metampicillin
- Talampicillin)
- Epicillin
- carboxypenicillins: Carbenicillin (Carindacillin)
- Ticarcillin
- Temocillin
- ureidopenicillins: Azlocillin
- Piperacillin
- Mezlocillin
- other: Mecillinam (Pivmecillinam)
- Sulbenicillin
|
|
|
Narrow sp.
|
|
β-lactamase sensitive
|
- Benzylpenicillin (G)#: Clometocillin
- Benzathine benzylpenicillin#
- Procaine benzylpenicillin#
- Azidocillin
- Penamecillin
- Phenoxymethylpenicillin (V)#: Propicillin
- Benzathine phenoxymethylpenicillin
- Pheneticillin
|
|
|
β-lactamase resistant
|
- Cloxacillin# (Dicloxacillin
- Flucloxacillin)
- Oxacillin
- Meticillin
- Nafcillin
|
|
|
|
|
Penems
|
|
|
|
Carbapenems
|
- Biapenem
- Ertapenem
- antipseudomonal (Doripenem
- Imipenem
- Meropenem)
- Panipenem
|
|
|
Cephalosporins/Cephamycins
(cephems)
|
|
1st (PEcK)
|
- Cefazolin#
- Cefacetrile
- Cefadroxil
- Cefalexin
- Cefaloglycin
- Cefalonium
- Cefaloridine
- Cefalotin
- Cefapirin
- Cefatrizine
- Cefazedone
- Cefazaflur
- Cefradine
- Cefroxadine
- Ceftezole
|
|
|
2nd (HEN)
|
- Cefaclor
- Cefamandole
- Cefminox
- Cefonicid
- Ceforanide
- Cefotiam
- Cefprozil
- Cefbuperazone
- Cefuroxime
- Cefuzonam
- cephamycin (Cefoxitin
- Cefotetan
- Cefmetazole)
- carbacephem (Loracarbef)
|
|
|
3rd
|
- Cefixime#
- Ceftriaxone#
- antipseudomonal (Ceftazidime#
- Cefoperazone)
- Cefcapene
- Cefdaloxime
- Cefdinir
- Cefditoren
- Cefetamet
- Cefmenoxime
- Cefodizime
- Cefotaxime
- Cefpimizole
- Cefpiramide
- Cefpodoxime
- Cefsulodin
- Cefteram
- Ceftibuten
- Ceftiolene
- Ceftizoxime
- oxacephem (Flomoxef
- Latamoxef ‡)
|
|
|
4th (antips-)
|
- Cefepime
- Cefozopran
- Cefpirome
- Cefquinome
|
|
|
5th
|
- Ceftobiprole
- Ceftaroline fosamil
|
|
|
Veterinary
|
- Ceftiofur
- Cefquinome
- Cefovecin
|
|
|
|
Monobactams
|
- Aztreonam
- Tigemonam
- Carumonam
- Nocardicin A
|
|
|
β-lactamase inh.
|
- penam (Sulbactam
- Tazobactam)
- clavam (Clavulanic acid)
|
|
|
Combinations
|
- Amoxicillin/clavulanic acid#
- Imipenem/cilastatin#
- Ampicillin/flucloxacillin
- Ampicillin/sulbactam (Sultamicillin)
- Piperacillin/tazobactam
|
|
|
| Other |
- polymyxins/detergent (Colistin
- Polymyxin B)
- depolarizing (Daptomycin)
- hydrolyze NAM-NAG (Lysozyme)
- Gramicidin
|
|
- #WHO-EM
- ‡Withdrawn from market
- Clinical trials:
- †Phase III
- §Never to phase III
|
|
|
gr+f/gr+a (t)/gr-p (c)/gr-o
|
drug (J1p, w, n, m, vacc)
|
|
|
|
