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Amitrim (Amitriptyline)
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Amitrim

Amitrim is used to treat mental/mood problems such as depression. Amitrim may help improve mood and feelings of well-being, relieve anxiety and tension, help you sleep better, and increase your energy level. Amitrim belongs to a class of medications called tricyclic antidepressants. It works by affecting the balance of certain natural chemicals in the brain.

Other names for this medication:
Amicure, Amidez, Amimax, Amitin, Amitop, Amitrim, Amitrip, Amitriptyline, Amitrol, Amitryptyline, Amitwix, Amline, Amoten, Amrea, Amsha, Amtipax, Amtran, Amypres, Arpidox, Bluneel, Chlotrip, Crypton, Emotrip, Endep, Eptanol, Estiline, Goldep, Kamitrin, Latilin, Libotryp, Librodep, Limbitrol, Limbival, Maxitrip, Mitryp, Nextrip, Psycomer, Relidep, Ristryl, Ronet, Sarotena, Sereval, Tablin, Teedep, Tridep, Tryptomec, Typteez

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Also known as: Amitriptyline

Description

Amitrim target is the treatment of depression. Amitrim is acting by increasing the amounts of certain natural substances in the brain that are needed to maintain mental balance. It is tricyclic antidepressant. Generic name of Amitrim is Amitriptyline. Amitrim is also known as Amitriptyline, Amitryptyline, Amidon, Amitryn, Tryptanol, Endep, Elatrol, Tryptizol, Trepiline, Laroxyl, Saroten, Triptyl, Amitrip. Brand names of Amitrim are Amitrim, Endep, Vanatrip.

Dosage

Take Amitrim tablets orally with water, with or without food. Take Amitrim for one to four times a day at the same time. The treatment can be resulting after 4 weeks. If you want to achieve most effective results do not stop taking Amitrim suddenly.

Overdose

If you overdose Amitrim and you don't feel good you should visit your doctor or health care provider immediately. Symptoms of Amitrim overdosage: seizures, loss of consciousness for a period of time, seeing things or hearing voices that do not exist, agitation, feeling drowsy, rigid muscles, vomiting, high temperature, cold body temperature, problems concentrating, abnormal heartbeats, confusion.

Storage

Store at room temperature between 20 and 25 degrees C (68 and 77 degrees F) away from moisture and heat. Throw away any unused medicine after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Amitrim are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.

Contraindications

You should not use Amitrim if you are allergic to amitriptyline, or:

if you have recently had a heart attack.

Do not use Amitrim if you have used an MAO inhibitor in the past 14 days. A dangerous drug interaction could occur. MAO inhibitors include isocarboxazid, linezolid, methylene blue injection, phenelzine, rasagiline, selegiline, tranylcypromine, and others.

Tell your doctor if you have used an "SSRI" antidepressant in the past 5 weeks, such as citalopram, escitalopram, fluoxetine (Prozac), fluvoxamine, paroxetine, sertraline (Zoloft), trazodone, or vilazodone.

To make sure Amitrim is safe for you, tell your doctor if you have ever had:

bipolar disorder (manic-depression) or schizophrenia; mental illness or psychosis; liver disease; heart disease; a heart attack, stroke, or seizures; diabetes (amitriptyline may raise or lower blood sugar); glaucoma; or problems with urination.

Some young people have thoughts about suicide when first taking an antidepressant. Your doctor should check your progress at regular visits. Your family or other caregivers should also be alert to changes in your mood or symptoms.

Tell your doctor if you are pregnant or breastfeeding.

Amitrim is not approved for use by anyone younger than 12 years old.

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Complications of subconjunctival 5-fluorouracil following glaucoma filtering surgery. Calcium-binding protein parvalbumin is associated with fast contracting muscle fibres. This analysis of the results of a randomized, controlled trial evaluating the effects of epoetin alfa (EPO) therapy on transfusion requirements, hemoglobin (Hb), and quality of life (QOL) in patients with cancer receiving platinum-based chemotherapy was conducted to evaluate the effect of initial Hb level on study outcomes. Histologically, the mesenteric tumor was composed of spindle cells showing both neural and smooth muscle differentiation. Neuronal expression of p53 dominant-negative proteins in adult Drosophila melanogaster extends life span. Quantitative T- and B-lymphocyte interrelationships in the peripheral blood in eczema patients in the process of naphthalane therapy using an immunomodulator. The highly polymorphic genes of the major histocompatibility complex (MHC) determine, in part, the odor cues and behavior of an individual.

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Murine models for autoimmune disease indicate the indispensable roles of the inhibitory Fc receptor in the suppression of such disorders, whereas activating-type FcRs are crucial for the onset and exacerbation of the disease. A cumulative dose-response study for metocurine was performed on 11 burned and 11 non-burned children during thiopentone, nitrous oxide in oxygen and narcotic anaesthesia. Influence of blanching treatments on Salmonella during home-type dehydration and storage of potato slices. The impact of taxing working memory on negative and positive memories. Two enzymes were purified from actinomycin-synthesizing Streptomyces chrysomallus which could be identified as peptide synthetases involved in the biosynthesis of actinomycin. Reinterventions after the Ross procedure are a concern for patients and treating physicians.

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The thalloid liverwort Plagiochasma rupestre supports arbuscular mycorrhiza-like symbiosis in vitro. Therapeutic interventions following loxosceles bites range from dapsone treatment to hyperbaric oxygen therapy, but the most promising therapy is the use of the antiserum, commercially available in certain South-American countries where loxosceles bites are common. The activities of glucose and gluconate dehydrogenases that are responsible for direct oxidation of glucose to 2-ketogluconic acid, were 2-3 times higher during the active growth of the culture than in the stationary phase. These barriers are brimming with fluids that bind, transport, cleave or degrade bacterial cells and their endotoxic by-products. A significant decrease in pump dysfunction and explantation was seen after 2007 compared to the period 2000-2007. Other standard laboratory tests were normal, as were absorptiometry measurements at the lumbar spine and femur. The presence of lymphocytes in L cell culture enhanced their differentiation, assessed by morphological, proliferative and biophysical criteria.

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