Cyclofenil

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Cyclofenil is a synthetic estrogenic compound that has been used in the treatment of various medical conditions, primarily in the field of gynecology and endocrinology. It is known to exert estrogen-like effects on certain tissues, while also possessing some anti-estrogen properties, making it a unique agent in the management of hormonal disorders.

Medical Uses[edit | edit source]

Cyclofenil has been utilized in the management of menstrual disorders, such as dysmenorrhea (painful menstruation) and amenorrhea (absence of menstruation). It has also been used in the treatment of infertility related to inadequate luteal phase support, by promoting the secretion of progesterone in the second half of the menstrual cycle. Additionally, cyclofenil has found application in the treatment of estrogen deficiency symptoms in postmenopausal women, offering an alternative to traditional hormone replacement therapy (HRT).

Mechanism of Action[edit | edit source]

Cyclofenil functions by binding to estrogen receptors (ER) in target tissues, which include the uterus, breasts, and brain. Its action is selective, as it can act as an estrogen agonist or antagonist depending on the tissue type and the presence of endogenous estrogen. In tissues where estrogen activity is needed, cyclofenil can mimic the effects of estrogen, whereas in tissues where estrogen's effects need to be mitigated, it can block the receptor and prevent estrogen's action.

Pharmacokinetics[edit | edit source]

The pharmacokinetic profile of cyclofenil includes its absorption, distribution, metabolism, and excretion (ADME) characteristics. After oral administration, cyclofenil is absorbed from the gastrointestinal tract. It undergoes extensive metabolism in the liver and is excreted primarily in the urine. The half-life of cyclofenil allows for once or twice daily dosing in most therapeutic applications.

Adverse Effects[edit | edit source]

While cyclofenil is generally well-tolerated, some individuals may experience side effects, which can include nausea, headache, and dizziness. Due to its estrogenic activity, there is a potential risk of stimulating the growth of estrogen-dependent tumors, and thus, it should be used with caution in individuals with a history of or predisposition to such conditions.

Contraindications[edit | edit source]

Cyclofenil is contraindicated in individuals with known hypersensitivity to the drug, as well as in those with a history of estrogen-dependent tumors. It should also be used with caution in patients with liver dysfunction, as its metabolism may be impaired.

Interactions[edit | edit source]

Drug interactions with cyclofenil can occur, particularly with medications that affect liver enzymes responsible for its metabolism. Such interactions can alter the effectiveness and safety profile of cyclofenil, necessitating adjustments in dosing or the consideration of alternative therapies.

Conclusion[edit | edit source]

Cyclofenil represents an important option in the management of certain gynecological and endocrinological disorders, offering benefits in cases where estrogenic or anti-estrogenic effects are desired. However, its use must be carefully considered in light of potential side effects, contraindications, and drug interactions.

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