Ditazole: Difference between revisions
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{{DISPLAYTITLE:Ditazole}} | |||
== | == Ditazole == | ||
Ditazole | [[File:Ditazole.svg|thumb|right|Chemical structure of Ditazole]] | ||
'''Ditazole''' is a [[non-steroidal anti-inflammatory drug]] (NSAID) that is used for its [[analgesic]], [[antipyretic]], and [[anti-inflammatory]] properties. It is a member of the [[azole]] class of compounds, characterized by the presence of a five-membered ring containing at least one nitrogen atom. | |||
Ditazole is | |||
== | == Mechanism of Action == | ||
Ditazole works by inhibiting the [[cyclooxygenase]] (COX) enzymes, which are responsible for the conversion of [[arachidonic acid]] into [[prostaglandins]]. Prostaglandins are lipid compounds that play a key role in the mediation of [[inflammation]], [[pain]], and [[fever]]. By reducing the production of prostaglandins, ditazole helps alleviate these symptoms. | |||
== | == Pharmacokinetics == | ||
After oral administration, ditazole is absorbed from the [[gastrointestinal tract]]. It is metabolized in the [[liver]] and excreted primarily through the [[kidneys]]. The half-life of ditazole varies depending on the dosage and individual patient factors. | |||
== | == Clinical Uses == | ||
Ditazole is used in the treatment of various conditions associated with pain and inflammation, such as: | |||
* [[Rheumatoid arthritis]] | |||
* [[Osteoarthritis]] | |||
* [[Musculoskeletal pain]] | |||
* [[Dysmenorrhea]] | |||
* [[ | |||
* [[ | |||
* [[ | |||
* [[ | |||
[[ | == Side Effects == | ||
[[Category: | Common side effects of ditazole include: | ||
[[Category: | * [[Gastrointestinal discomfort]] | ||
* [[Nausea]] | |||
* [[Dizziness]] | |||
* [[Headache]] | |||
Serious side effects, although rare, may include: | |||
* [[Gastrointestinal bleeding]] | |||
* [[Allergic reactions]] | |||
* [[Renal impairment]] | |||
== Contraindications == | |||
Ditazole should not be used in patients with: | |||
* Known hypersensitivity to ditazole or other NSAIDs | |||
* Active [[peptic ulcer disease]] | |||
* Severe [[hepatic]] or [[renal impairment]] | |||
== Related pages == | |||
* [[Non-steroidal anti-inflammatory drug]] | |||
* [[Cyclooxygenase]] | |||
* [[Prostaglandin]] | |||
[[Category:Non-steroidal anti-inflammatory drugs]] | |||
[[Category:Azoles]] | |||
Latest revision as of 03:47, 13 February 2025
Ditazole[edit]

Ditazole is a non-steroidal anti-inflammatory drug (NSAID) that is used for its analgesic, antipyretic, and anti-inflammatory properties. It is a member of the azole class of compounds, characterized by the presence of a five-membered ring containing at least one nitrogen atom.
Mechanism of Action[edit]
Ditazole works by inhibiting the cyclooxygenase (COX) enzymes, which are responsible for the conversion of arachidonic acid into prostaglandins. Prostaglandins are lipid compounds that play a key role in the mediation of inflammation, pain, and fever. By reducing the production of prostaglandins, ditazole helps alleviate these symptoms.
Pharmacokinetics[edit]
After oral administration, ditazole is absorbed from the gastrointestinal tract. It is metabolized in the liver and excreted primarily through the kidneys. The half-life of ditazole varies depending on the dosage and individual patient factors.
Clinical Uses[edit]
Ditazole is used in the treatment of various conditions associated with pain and inflammation, such as:
Side Effects[edit]
Common side effects of ditazole include:
Serious side effects, although rare, may include:
Contraindications[edit]
Ditazole should not be used in patients with:
- Known hypersensitivity to ditazole or other NSAIDs
- Active peptic ulcer disease
- Severe hepatic or renal impairment