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Amitop (Amitriptyline)
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Amitop

Amitop is not FDA-approved to treat insomnia (trouble falling or staying asleep), but one of the side effects of the medication is sleepiness, especially when you first start taking it. Because of this, you may want to take it in the evening or before bedtime when you first start taking it.

Other names for this medication:
Abamax, Amiclozor, Amicure, Amitrim, Amitrip, Amitrol, Amitryn, Amitryptyline, Amitwix, Amity, Amrea, Aptric, Arpidox, Chlotrip, Cotrip, Estiline, Libral, Librodep, Limbitrol, Lodep, Maxitrip, Mitrip, Psycomer, Raitrip, Ristryl, Ronet, Sarotena, Sereval, Tridep, Trixide, Tryline, Typlin, Typteez

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Also known as: Amitriptyline

Description

Amitop target is the treatment of depression. Amitop 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 Amitop is Amitriptyline. Amitop is also known as Amitriptyline, Amitryptyline, Amidon, Amitryn, Tryptanol, Endep, Elatrol, Tryptizol, Trepiline, Laroxyl, Saroten, Triptyl, Amitrip. Brand names of Amitop are Amitop, Endep, Vanatrip.

Dosage

Usual Adult Dose for Depression:

OUTPATIENTS: -Initial dose: 75 mg orally per day in divided doses; this may be increased to 150 mg/day (if needed) -Maintenance dose: 40 to 100 mg orally per day -Maximum dose: 150 mg/day Alternate outpatient treatment regimen: 50 to 100 mg orally as a single dose at bedtime; this may be increased by 25 or 50 mg as needed at bedtime to a total of 150 mg/day INPATIENTS: -Initial dose: 100 mg orally per day -Maintenance dose: 40 to 100 mg orally as a single dose at bedtime -Maximum dose: 300 mg/day Comments: -Dose increases should preferably be made in the late afternoon or at bedtime due to the sedative effect. -The full therapeutic effect may take as long as 30 days to develop. -Maintenance doses should be reduced to the lowest amount that will maintain relief of symptoms when satisfactory improvement has been obtained. -Maintenance therapy should be continued for 3 months or longer to lessen the possibility of relapse. Use: Relief of symptoms of depression

Usual Geriatric Dose for Depression:

10 mg orally 3 times a day AND 20 mg orally once a day at bedtime Comments: -The full therapeutic effect may take as long as 30 days to develop. -Elderly patients should be monitored carefully and serum levels obtained as clinically appropriate. -Dose adjustments should be made according to clinical response. Use: Relief of symptoms of depression

Usual Pediatric Dose for Depression:

12 years or older: 10 mg orally 3 times a day AND 20 mg orally once a day at bedtime Comments: -The full therapeutic effect may take as long as 30 days to develop. -Dose adjustments should be made according to clinical response. Use: Relief of symptoms of depression

Detailed Amitop dosage information

Overdose

If you overdose Amitop and you don't feel good you should visit your doctor or health care provider immediately. Symptoms of Amitop 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 Amitop 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 Amitop if you are allergic to amitriptyline, or:

if you have recently had a heart attack.

Do not use Amitop 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 Amitop 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.

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

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The purpose of this study is to compare outcomes between patients treated with CRT that attained a cCR and opted for a vigilant surveillance to those of the patients who had a complete pathologic response (cPR) following proctectomy. Patients with shallow anterior chambers found in routine health examinations were evaluated with UBM scan. Both offensive and defensive sperm competitive abilities were found to be significantly repeatable only across matings involving ejaculates of the same pair of males competing within the same female. Alteration of domain architectural complexity of signaling proteins and repeated lineage-specific reshaping of architectures might have played a major role in the emergence of new signaling interactions in different eukaryotes. The results reveal the potential of the proposed informatics system for computer-aided IVD diagnosis from MRI in large-scale research studies and as a possible adjunct for clinical diagnosis. ST-segment elevation myocardial infarction caused by pLAD compared with mLAD occlusion results in larger infarcts and greater mortality even with contemporary reperfusion therapy. The experimental results showed that phosphorus existed in a more stable form with capping than without capping.

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In recent years, the number of cases in which a ventricular assist device is required for serious heart failure not responding to conventional mechanical circulatory assistance, has been increasing. The pyloric region was characterized by the presence of abundant gastrin-, somatostatin-, and neurotensin-immunoreactive cells. The synthetic approach takes advantage of disulfide chemistry to specifically modify only the cysteine residues within peptides and covalently links C16 groups via disulfide bridges using a new thioalkylating reagent, hexyldexyldithiopyridine. Breast cancer diagnosis using self-organizing map for sonography. Interaction between the renal excretion rates of beta 2-microglobulin and gentamicin in man. Here, we report the discovery and characterization of a second generation clinical MDM2 inhibitor, RG7388, with superior potency and selectivity.

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Highly sensitive covalently functionalized light-addressable potentiometric sensor for determination of biomarker. We describe the TX system which incorporates ventricular pacing and is driven by T wave sensing determined by the QT interval. Immunization with CAT or GLU constructs resulted in significantly reduced dental caries after infection with S. These results suggest that the B19 parvovirus promoter includes a complex regulatory region containing multiple sequences which affect promoter strength and that the GC-box motif is a major controlling sequence for in vitro transcription. We aimed to evaluate the liver disease stages of patients with HCV-NHL.

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Disease-free survival and overall survival are equivalent between patients treated with neoadjuvant chemotherapy and patients treated with the same regimen postoperatively. Development of a solid phase extraction procedure for HPLC-DAD determination of several angiotensin II receptor antagonists in human urine using mixture design. In this article, the recent patients relating to bird flu infection covering the diagnostic and treatment aspects for both avian species and human are reviewed and discussed. Pyridine was used as odorant in four different concentrations investigating the ability to detect the stimulus and the acuity to estimate its intensity. Due to their properties, microbial SACs have been exploited in environmental remediation techniques. Acute Luminal Gain after Stenting: Comparison of Gianturco-Roubin and Palmaz-Schatz Stents. This case highlights the essential diagnostic and therapeutic features of a common malignancy seen primarily in young men. The distribution of the fat tissue in the subcutaneous layer is described. We have developed an Escherichia coli system for expression, solubilization and purification of the adrenal cytochrome. A simplified method for detecting macroamylasemia by measuring serum amylase activity at different reaction temperatures.

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