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Clomifene Cirtrate is a nonsteroidal, ovulatory stimulant used to treat ovulatory dysfunction and polycystic ovary syndrome in women who, after other reasons for pregnancy failure have been ruled out, desire pregnancy and follow additional instructions that make pregnancy more likely to occur with this drug use (see below about dosage and use).It works by stimulating an increase in the amount of hormones that support the growth and release of a mature egg (ovulation).
Clominorex is a centrally acting sympathomimetic which is related to other drugs such as aminorex and pemoline. It was developed as an appetite suppressant.
Clomifene is a selective estrogen receptor modulator that increases production of gonadotropins by inhibiting negative feedback on the hypothalamus. It is used mainly for ovarian stimulation in female infertility due to anovulation.
Clomipramine is a tricyclic antidepressant. It had been used experimentally to reduce relapses in cocaine addicts, and to repair neurotransmitter damage caused by cocaine. It has also been used experimentally to treat dogs with severe anxiety disorders, OCD, or cognitive dysfunction syndrome.
Clomocycline is a tetracycline antibiotic that inhibits bacterial cell growth by inhibiting translation. It is lipophilic and easily diffuses across cell membranes or enters cells via porin channels in the bacterial membrane. It binds to the 30S ribosomal subunit and prevents the aminoacyl tRNA from binding to the A site of the ribosome-RNA complex. Clomocycline binding is reversible in nature. It may be used to treat acne, gum disease, and other bacterial infections such as chalmydia, brucellosis, bartonellosis and cholera. It is also effective against certain strains of malaria and may also be prescribed for the treatment of Lyme disease.
Clonazepam is a benzodiazepine derivative having anticonvulsant, muscle relaxant, and very potent anxiolytic properties. It is a chlorinated derivative of nitrazepam and therefore a nitrobenzodiazepine. Benzodiazepines such as clonazepam have a fast onset of action and high effectiveness rate and low toxicity in overdose but have drawbacks due to adverse reactions including paradoxical effects, drowsiness, and cognitive impairment. Cognitive impairments can persist for at least 6 months after withdrawal of clonazepam; it is unclear whether full recovery of memory functions occurs.
Clonidine is a medication used to treat several medical conditions. It is a direct-acting α2 adrenergic agonist and an imidazoline. It has been prescribed historically as an antihypertensive drug. It has found new uses, including treatment of some types of neuropathic pain, opioid detoxification, sleep hyperhidrosis, anaesthetic use, and off-label, to counter the side effects of stimulant medications such as methylphenidate or amphetamine. It is becoming a more accepted treatment for insomnia, as well as for relief of menopausal symptoms. It is increasingly used in conjunction with stimulants to treat attention-deficit hyperactivity disorder, for which it is administered in late afternoon or evening for sleep, and because it sometimes helps moderate ADHD-associated impulsive and oppositional behavior, and may reduce tics, a problem in which a part of the body moves repeatedly, quickly, suddenly and uncontrollably. Clonidine can be used in the treatment of Tourette syndrome. Its epidural use for pain during heart attack, postoperative and intractable pain has also been studied extensively. It has also been used to treat the hyperarousal symptoms of PTSD. It is also a mild sedative, and can be used as premedication before surgery or procedures. This medication may also be used to ease withdrawal symptoms associated with the long-term use of narcotics, alcohol and nicotine. In addition, clonidine has also been used for migraine headaches and hot flashes associated with menopause.
Clonitazene is an opioid analgesic of approximately three times the potency of morphine. It is related to etonitazene.
Clonixin is a non-steroidal anti-inflammatory drug. It also has analgesic, antipyretic, and platelet-inhibitory actions. It is used primarily in the treatment of chronic arthritic conditions and certain soft tissue disorders associated with pain and inflammation.
Clopenthixol is a typical antipsychotic drug of the thioxanthene class. It was introduced by Lundbeck in 1961. It is a racemic mixture of cis and trans isomers. Zuclopenthixol, the pure cis isomer, was later introduced by Lundbeck in 1962, and has been much more widely used. Both drugs are equally effective as antipsychotics and have similar adverse effect profiles, but clopenthixol is half as active on a milligram-to-milligram basis and appears to produce more sedation in comparison.
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