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Aurex (Citalopram)

Aurex is an antidepressant medication that works in the brain. It is approved for the treatment of major depressive disorder (MDD). Aurex may also be helpful when prescribed “off-label” for obsessive-compulsive disorder, panic disorder, social phobia (also known as social anxiety disorder), posttraumatic stress disorder, eating disorders, premenstrual dysphoric disorder, and alcohol dependence. “Off-label” means that it hasn’t been approved by the Food and Drug Administration for this condition. Your mental health provider should justify his or her thinking in recommending an “off-label” treatment. They should be clear about the limits of the research around that medication and if there are any other options.

Other names for this medication:
Citalopram, Celexa, Akarin, Arpolax, Aurex, Belmazol, Calton, Celapram, Celius, Ciazil, Cilift, Cimal, Ciprager, Cipram, Cipramil, Ciprapine, Ciprotan, Cital, Citalec, Citapram, Citara, Citaxin, Citol, Citopam, Citox, Citrex, Citrol, Citronil, Dalsan, Depramil, Elopram, Eostar, Humorap, Hydertan, Laira, Lopram, Lopraxer, Opra, Oropram, Prisdal, Proximax, Relaxol, Sepram, Seropram, Somac, Talohexal, Talosin, Temperax, Verisan, Vodelax, Zebrak, Zentius,

Similar Products:
Afungil, Sergel, Kipferon, Vidalista, Gabapentina, Efferven, Amoxi, Keftab, Azelastina, Geramox, Cefodox, Aldactazide, Glaveral, Stocrin, Amoxicilina, Alizar, Mebendazol, Zipantola, Tefilin, Zoloft, Proxime, Ranitidina, Oftaquix, Senexon, Alprostadil,

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An effective drug delivery system delivers the therapeutically active moieties at the right time, rate and in a reproducible manner to target sites for the effectively the human illnesses. The purpose of this study was to find a simple, effective 1-step articular cartilage repair method.

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Labeled fiber terminals were identified in the dorsal horn and the central cervical nucleus in the spinal cord, and in the intermediate nucleus, cuneate nucleus, external cuneate nucleus and the caudal portion of the nucleus of the solitary tract (NTS) in the brainstem. Interaction of DHS-I with maxi-K channels from bovine aortic smooth muscle was studied after incorporating single channels into planar lipid bilayers.

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