m Changed protection level for "Articaine" ([Edit=Allow only autoconfirmed users] (expires 12:02, 9 July 2014 (UTC)) [Move=Allow only autoconfirmed users] (expires 12:02, 9 July 2014 (UTC)))
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{{SI}}
{{PillImage
'''Articaine''' is a dental local anesthetic. It is manufactured and distributed by Septodont under the brand name Septocaine. Articaine hydrochloride 4% with [[epinephrine]] 1:100,000 injection. Septocaine was first approved for use in Germany in 1976 and throughout Europe shortly after. Canada approved usage in 1982, with the US FDA following in 2000. Qualities such as fast acting nature and strength of dosage have made it more appealing for use by dentists than other available anesthetics such as [[novocaine]] and [[lidocaine]].
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== Structure and Metabolism ==
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Articaine is unique among local anesthetics because it contains a [[thiophene]] group, and also because it contains both [[ester]] and [[amide]] groups. Articaine is an amide anesthetic due to the amide intermediate chain, and undergoes hepatic metabolism. However, the associated ester group also allows plasma metabolism via pseudocholinesterase, purportedly increasing the rate of breakdown and reducing its toxicity. This difference in metabolism gives articaine the distinct advantage of having a 30 minute half life, as opposed to drugs such as lidocaine that have a 90 min. half life.
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== Complications ==
NO Serious complications have been associated with Septocaine. Long-term or transient [[paresthesia]] is among the worst of the reported side effects of Septocaine but does not occur as frequently as with lidocaine. (JD)
It should be noted that almost all recorded cases of long term numbness or parasthesia in a dental setting are associated with a mandibular nerve block type injection and simple infiltration injections are generally thought to be immune from such complications. For this reason many dentists have abandoned using articaine for mandibular nerve blocks.
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Black Box Warning
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See full prescribing information for complete Boxed Warning.
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Overview
Articaine is a {{{drugClass}}} that is FDA approved for the {{{indicationType}}} of {{{indication}}}. There is a Black Box Warning for this drug as shown here. Common adverse reactions include .
Adult Indications and Dosage
FDA-Labeled Indications and Dosage (Adult)
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Off-Label Use and Dosage (Adult)
Guideline-Supported Use
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There is limited information regarding Off-Label Guideline-Supported Use of Articaine in adult patients.
Non–Guideline-Supported Use
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There is limited information regarding Off-Label Non–Guideline-Supported Use of Articaine in adult patients.
Pediatric Indications and Dosage
FDA-Labeled Indications and Dosage (Pediatric)
Condition1
Dosing Information
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There is limited information regarding FDA-Labeled Use of Articaine in pediatric patients.
Off-Label Use and Dosage (Pediatric)
Guideline-Supported Use
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Developed by:
Class of Recommendation:
Strength of Evidence:
Dosing Information
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There is limited information regarding Off-Label Guideline-Supported Use of Articaine in pediatric patients.
Non–Guideline-Supported Use
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There is limited information regarding Off-Label Non–Guideline-Supported Use of Articaine in pediatric patients.
Contraindications
Condition1
Warnings
ConditionName:
See full prescribing information for complete Boxed Warning.
ConditionName:
Content
Description
Precautions
Description
Adverse Reactions
Clinical Trials Experience
There is limited information regarding Clinical Trial Experience of Articaine in the drug label.
Body as a Whole
Cardiovascular
Digestive
Endocrine
Hematologic and Lymphatic
Metabolic and Nutritional
Musculoskeletal
Neurologic
Respiratory
Skin and Hypersensitivy Reactions
Special Senses
Urogenital
Miscellaneous
Postmarketing Experience
There is limited information regarding Postmarketing Experience of Articaine in the drug label.