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Trazodon (Trazodone)
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Trazodone

Trazodon oral tablet is a prescription drug. It’s available only as a generic drug. Generic drugs usually cost less than brand-name drugs. Trazodon is used to treat depression in adults. Trazodon belongs to a class of drugs called antidepressants. A class of drugs is a group of medications that work in a similar way. These drugs are often used to treat similar conditions. It isn’t fully understood how Trazodon works. It may increase serotonin activity in your brain. Serotonin is a chemical in your brain that can help stabilize your mood.

Other names for this medication:
Trazodone, Desyrel, Azona, Donaren, Mesyrel, Nestrolan, Oleptro, Reslin, Trant, Trazodon, Trazodona,

Similar Products:
Planor, Aricept, Tamec, Dival, Finast, Secalip, Vals, Liperial, Lipicon, Ucerax, Ramicor, Zient, Celcox, Biomoxil, Rheumatac, Spiron, Bisoce, Aquazide, Zodem, Benicar, Celtium, Clavumox, Promoxil, Onapil, Ulcoreks, Aroxin, Concore, Lopo, Isoptin, Rebetron, Lanton, Wymox, Drusa, Cital, Dols, Dolex, Paine, Tramex, Zotrole, Ozepran, Torivas, Tenofovir, Amoxival, Indophtal, Longamox, Pantocalm, Norilet, Biocid,

Trazodon comes as a tablet and as an extended-release (long-lasting) tablet to take by mouth. The tablet is usually taken with a meal or light snack two or more times a day. The extended-release tablet is usually taken once a day at bedtime on an empty stomach, either one hour before or two hours after a meal. To help you remember to take Trazodon, take it around the same time every day. Follow the directions on your prescription label carefully, and ask your doctor or pharmacist to explain any part you do not understand. Take Trazodon exactly as directed. Do not take more or less of it, take it more often, or take it for a longer time than prescribed by your doctor.

Swallow the extended-release tablets whole or broken in half on the score mark; do not chew or crush them.

Your doctor may start you on a low dose of Trazodon and gradually increase your dose, not more than once every 3 to 4 days. Your doctor may decrease your dose once your condition is controlled.

Trazodon controls depression, but does not cure it. It may take 2 weeks or longer before you feel the full benefit of Trazodon. Continue to take Trazodon even if you feel well.

Do not stop taking Trazodon without talking to your doctor. If you suddenly stop taking Trazodon, you may experience withdrawal symptoms such as anxiety, agitation, or difficulty falling asleep or staying asleep. Your doctor will probably decrease your dose gradually.

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Several characters of the chick intestinal sucrase resembled those of the intestinal sucrase-isomaltase complex of some mammals (rabbit, rat and human). Such data could assist in advocacy for these patients and should influence end-of-life care strategies in hospital. Splenocytes from MOG-immunized lit/lit mice proliferated normally in response to MOG peptide, suggesting that activation of MOG-specific T cells in GHRHR-deficient mice is not impaired.

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Characterization of new DsbB-like thiol-oxidoreductases of Campylobacter jejuni and Helicobacter pylori and classification of the DsbB family based on phylogenomic, structural and functional criteria. These data suggest that purine nucleotides act as proliferation signals for neural progenitor cells, and thereby serve as negative regulators of terminal neuronal differentiation.

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Surgical treatment of arteriovenous angiomas localised in the corpus callosum, basal ganglia and near the brain stem. Quality of life of nursing home residents with dementia: validation of the German version of the ICECAP-O.

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Angiotensin receptor blocker selectivity at the AT1- and AT2-receptors: conceptual and clinical effects. Posttraumatic stress disorder (PTSD) is a chronic and debilitating anxiety disorder. Acute transverse myelitis with urinary retention due to mycoplasma pneumoniae infection: a case report

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This paper discusses different routes to gaining insight from closed loop learning control experiments. The process of liver damage was fulminant with massive diffuse centrilobular necroses, lymphoid-eosinophilic infiltration in the portal tracts, and the development of liver failure. ABCA1-stimulation inhibited HCV cell entry, acting on virus-host cell fusion, but had no impact on virus attachment, replication, or assembly/secretion.

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Early administration of infliximab for severe ipilimumab-related diarrhea in a critically ill patient. These data suggest that oral pirenzepine may have a therapeutic potential for preventing malignant ventricular arrhythmias after infarction. Neither the enhanced nor the reduced trkB activity influenced MK-801-induced neurotoxic effects in the posterior cingulate cortex of mouse brain, which indicates that increased BDNF production neither protects nor exacerbates neurotoxic effects of NMDA receptor antagonists. The in vitro antimalarial activity of a series of 2- and 8-trifluoromethyl- and 2,8-bis(trifluoromethyl)quinoline-4-(5-pyrimidino) and N4-ethyl-5-nitroimidazolo)methylene ketones was assessed against the chloroquine-sensitive strain (D10) of Plasmodium falciparum. We demonstrate that stable mixed donor:host hematopoietic chimerism, achieved by a non-myeloablative bone marrow transplant from a histocompatible littermate, reverses the disease phenotype in CLAD.

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