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Common side effects include trouble sleeping, nausea, sexual problems, and feeling tired. Escitalopram was approved for medical use in the United States in Escitalopram has FDA approval for the treatment of major depressive disorder in adolescents and adults, and generalized anxiety disorder in adults. In Australia it is approved for major depressive disorder. Escitalopram was approved by regulatory authorities for the treatment of major depressive disorder on the https://business.amwell.com basis of four placebo controlled, double-blind trials, three of which demonstrated a statistical superiority over placebo. Controversy existed regarding the effectiveness of escitalopram compared with its predecessor, citalopram. Escitalopram appears effective in treating social anxiety disorder. Escitalopram, as well as other SSRIs, is effective in reducing the symptoms of premenstrual syndrome, whether taken in the luteal phase only or continuously.

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Escitalopram affects chemicals in the brain that may become unbalanced and cause depression and anxiety. It is used to treat depression, obsessive-compulsive disorder OCD, and generalized anxiety disorder GAD in adults and adolescents who are at least 12 years old. The recommended starting dose is 10mg per day, which is also the maintenance dose for many patients. We also carry the generic S Citadep is manufactured in India by Cipla. Do not take this medication if you are allergic to escitalopram, citalopram, or any ingredients of the medication. It is known that the medication citalopram, which is similar to escitalopram, passes into breast milk. If you are a breast-feeding mother and are taking escitalopram, it may affect your baby. Talk to your doctor to see if you should continue breast-feeding. There may be an interaction between escitalopram and other medications such as: alcohol, fluconazole, itraconazole, lithium, omeprazole, pimozide, quinine, tetrabenazine, warfarin, etc.

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Urinary excretion of phenytoin and its metabolites occurs partly with glomerular filtration but more importantly by tubular secretion. Because phenytoin is hydroxylated in the liver by an enzyme system which is saturable at high plasma levels, small incremental doses may increase the half-life and produce very substantial increases in serum levels, when these are in the upper range.


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