Most popular brand: Strattera
Active ingredient: Atomoxetine
Available dosage forms: 10, 25, 40 mg
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Atomoxetine general information
There were not any serious adverse events associated with atomoxetine. In addition, He was in the principals office three or more times weekly. Our measures may also have limited our capacity to detect changes. Also will not seem to be physically addictive.
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Those that have taken the drug on a long-term (i.e. years) might notice that a number of the weight they lost after a moderate period of time began to return. Some folks report significant weight reduction during the very first few weeks of remedy, but the upcoming few weeks they might gain all that weight back. Generally this is a somewhat considerable quantity of weight to lose in this kind of short-term, but might happen.
I began looking into medication this past year. The sole side effect we noticed was he would get a bit more whiney than usual within the evening, once the medication was wearing off. When that was corrected, the patient managed to sleep again and managed to work at a superior rate. 100 mg every day taken once before bed for the time of two years nausea in the beginning, agitation in the beginning, sleeplessness initially.
The dosage in relationship to your own weight probably will play a part in determining simply how much weight you wind up losing. 1 person may shed weight as they are extremely nauseous, while another may shed weight simply since the drug speeds their metabolism. Understand you can have a certain pack of genes that make you more probable to shed weight on Strattera. It may likewise be used to treat or protect against low blood potassium.
Since different individuals react differently to Strattera in regard to weight, it’s vital to know why. It’s also crucial to stay in mind that anytime a drug is stimulating, it might give a person more energy which they can utilize to participate in physical activity which likewise results in weight loss. 6 Atomoxetine doesn’t have monoamine releasing effects, thus isn’t considered to possess the abuse potential of stimulants. 2 Antiobesity drugs are demonstrated to improve weight loss when combined with interventions geared toward modifying lifestyle.
In the event of men, thinning or lack of hair in the hairline or leading of the head consist of a number of the normal indications of baldness. This is mainly due to how these drugs are inclined to make people gain weight. Modest weight reduction can cut back health risks related to obesity.
After four years of using Stratterra, I wouldn’t ever switch to another ADHD medication. Other drugs are taken in conjunction with strattera to assist the patient function for an optimal level every day. Ideal solution seems to be to choose the meds with or following food, and also to attempt to acquire a decent quantity of sleep. I wondering if altering the dose will provide help.
Stimulants pills are used to heal ADD for at least three decades. Non stimulant therapy, the 2nd line treatment for ADHD, involves the application of non-stimulant drugs. You might also wish to consider an all-natural alternative to the medications mentioned previously. Buproprion SR and XL have also been applied for remedying adults, but it’s less effective in comparison to amphetamine.
It’s as vital that you sleep at the proper time (in a continuous, uninterrupted manner) as it’s in order to get enough of it. Codeine and selegiline can also be used to take care of narcolepsy symptoms. Such chemical imbalances may occur because of the aforementioned changes which might be related to anxiety as well as depression. Chantix is believed to cause homicidal ideas and actions because of its capacity to boost a neurotransmitter called dopamine within the brain.
Although nearly every sort of prescription drug is is more than likely to be abused in a single way or another, there are lots of types of prescription drugs which are abused more frequently than many others. It’s a widely held belief that a lot of medications used to take care of symptoms of ADHD are similar inside their effectiveness. Side effects are usually mild, and have a tendency to decrease or disappear when the patient has been taking the medication for some time. If other medications are tried and aren’t effective for a patient, it’s likely that a more powerful variation is required.
Ignoring ADHD may be equally dangerous. Also people that have epilepsy are at a greater risk for ADHD. Medication isn’t a cure, but may be an invaluable assistance. The objective of medication is to trim the symptoms with the purpose to provide the child the liberty to learn academic, social, and other life skills.
Atomoxetine: information for professionals
Atomoxetinum ( genus. Atomoxetini)
Pharmacological action. Highly selective potent inhibitor of presynaptic norepinephrine vectors with minimal affinity for the other. Noradrenergic receptors, as well as others. Receptors of neurotransmitters. It does not apply to psychostimulants and is not derived from amphetamine. Syndrome “cancellation” is not marked.
The pharmacokinetics. Quickly and almost completely absorbed after oral administration. T C max ; 1 –. 2 hours well distributed in the body. Communication with proteins ; high (especially albumin). It is metabolized in the liver involving the cytochrome CYP2D6. The main image is oxidized metabolite 4 – gidroksiatomoksetin glyukuroniruetsya quickly. By pharmacological activity equivalent atomoxetine but circulates in plasma at much lower concentrations. People with inadequate activity of CYP2D6 4 – gidroksiatomoksetin can be formed using other cytochrome P450 isoenzymes, but more slowly.. T 1/2 ; 3.6 hours in patients with high intensity and 21 h metabolism ; with reduced. Shown mainly in the urine as 4 – gidroksiatomoksetin – About – glyukuronida.Farmakokinetika in children and adolescents is similar to the pharmacokinetics in adults.
Indications. Attention Deficit Hyperactivity Disorder.
Contra. Hypersensitivity, angle-closure glaucoma, simultaneous reception of MAO inhibitors. lactation, children’s age (up to 6 years).
with caution. Hypertension, tachycardia, stroke, hypotension, and the disease, its cause, pregnancy.
Dosing Inside, regardless of meals (or during meals), 1 time per day in the morning or in the event of side effects .; 2 times a day (morning and late afternoon or early evening).
Children and adolescents with a body weight up to 70 kg: the recommended initial daily dose of ; 0.5 mg / kg, which was increased to 1.2 mg / kg, not earlier than 3 days. If there is no improvement of the daily dose can be increased to a maximum ; 1.8 mg / kg (or 120 mg) no earlier than 2 – 4 weeks after starting the drug.
The recommended maintenance dose ; 1.2 mg / kg / day.
Children and adolescents weighing over 70 kg and adults: The recommended initial daily dose of ; 40 mg, which was increased to 80 mg not earlier than 3 days. If there is no improvement of the daily dose can be increased to a maximum ; 120 mg not earlier than 2 – 4 weeks after starting the drug. The recommended maintenance dose ; 80 mg.
In patients with moderate hepatic impairment (class B classification Child – Pugh) starting and maintenance dose is reduced by 50%. In patients with severe hepatic impairment (Class C classification Child – Pugh) starting and maintenance dose is reduced to 25% of the usual dose of.
Side effects Very often (more than 10%), often (1 – 10%)., Not often (0,1 – 1%).
Children and adolescents: the most frequently ; abdominal pain, loss of appetite (18% and 16% respectively).
In connection with the reduction of appetite reduction in body weight was observed at the beginning of treatment an average of 0.5 kg (weight loss increased at higher doses). After the initial weight loss, it showed a slight increase in body mass during prolonged therapy. Development Indicators (weight and height) after 2 years of treatment are close to normal. There were nausea and vomiting (9% and 11% respectively), especially during the first month of treatment, increased heart rate 6 / min, systolic and diastolic blood pressure of 2 mm Hg.
From the nervous system: often ; dizziness, drowsiness, early morning awakening, irritability, emotional lability.
From the senses: frequently ; mydriasis.
From the CCC. often not ; palpitations, sinus tachycardia.
From the digestive system: very often ; abdominal pain, vomiting; frequently ; dyspepsia (including constipation, nausea).
For the skin: often ; dermatitis, pruritus, rash.
From a metabolism: very often ; loss of appetite; frequently ; anorexia, weight loss.
Allergic reactions: skin rash, angioedema, urticaria.
Others: frequently ; fatigue, flu.
The following adverse events occurred in 2% of patients with low activity of Cytochrome CYP2D6 were 2 times or more statistically significantly more often in patients with reduced metabolism compared to patients with high activity of CYP2D6. appetite reduction (24.1% and 17% respectively), insomnia (10.5% and 6.8%, respectively), quality of sleep disturbance (3.8% and 1.5%, respectively), enuresis (3% and 1, 2%, respectively), low mood (3% and 1%, respectively), tremor (5.1% and 1.1%, respectively), early morning awakening (3% and 1.1%, respectively), conjunctivitis (3% and 1 5%, respectively), syncope (2.1% and 0.7%, respectively), mydriasis (2.5% and 0.7% respectively). In adults: increase in heart rate of 6 / min, systolic blood pressure by 3 mm Hg diastolic and 1 mm Hg .; orthostatic hypotension (0.2%), syncope (0,8%).
From the nervous system: very often ; insomnia; frequently ; dizziness, sleep quality violation, headache, early morning awakening, decreased libido, insomnia, drowsiness, weakness.
From the CCC. frequently ; “Tides” of blood, palpitation, tachycardia; often not ; cold sensation in the lower extremities.
From the digestive system: very often ; dry mouth, nausea; frequently ; abdominal pain, dyspepsia (including constipation, flatulence).
From a metabolism: very often ; loss of appetite; frequently ; weight loss.
For the skin: often ; dermatitis, increased sweating.
With the genitourinary system: often ; difficulty urinating, urinary retention, dysmenorrhea, abnormal ejaculation and erection, orgasm disturbance, prostatitis.
Allergic reactions: skin rash, angioedema, urticaria.
Overdose Symptoms:. Drowsiness, agitation, hyperactivity, conduct disorder, disturbance of the digestive tract function. mydriasis, tachycardia, dry mouth, seizures. Reported cases of acute overdose with fatal outcome while taking atomoxetine in combination with others. PM.
Treatment: gastric lavage, activated charcoal, monitoring heart activity and vital signs, ventilator. symptomatic and supportive therapy. Dialysis is not effective..
Interaction Atomoxetine should not be used for a minimum of 2 – weeks after discontinuation of MAO inhibitors. MAO inhibitors treatment should begin within 2 – weeks after the lifting of Atomoxetine.
Beta 2 – adrenostimulyatorov ; the risk of side effects from the CCC (increased heart rate and blood pressure).
It does not cause clinically significant inhibition or induction of cytochrome P450 isoenzymes, including SYP1A2. CYP3A. CYP2D6 and CYP2C9.
Patients with severe metabolic CYP2D6 inhibitors CYP2D6 Atomoxetine increase the concentration in plasma to a level similar to that of patients with reduced metabolism of CYP2D6.
vasoconstrictive drugs ; the risk of increased blood pressure.
PM. raising the pH of gastric juice (hydrochloride magnesium / aluminum hydroxide, omeprazole) does not affect the bioavailability of Atomoxetine.
PM. affecting the secretion of norepinephrine ; may increase or synergistic effect.
Special instructions. Treatment should be under the supervision of a doctor who has experience of working with patients with a syndrome of concentration of attention deficit hyperactivity disorder.
Cancel the drug does not require a gradual reduction of the dose.
On the background of the drug in clinical trials in children and adolescents increases the risk of suicidal thoughts. During these clinical studies reported a suicide attempt; completed suicide was not.
Many patients during the treatment period there was an increase in heart rate (less than 10 / min) and / or increase in blood pressure (less than 5 mm Hg), which in most cases had no clinical significance.
Cases of orthostatic hypotension have been reported, therefore caution should be exercised when administering the drug for conditions and diseases, leading to hypotension.
In the case of jaundice or laboratory test abnormality, indicative of abnormal liver function, treatment of atomoxetine should be abolished. Rarely, hepatotoxicity manifested by increased activity of “liver” enzymes, hyperbilirubinemia and jaundice.
The efficacy and safety in children under 6 years of age and in elderly patients has not been established. The effectiveness of treatment for over 1.5 years, as well as safety for the duration of therapy more than 2 years has not been studied.
In children and adolescents weighing more than 70 kg and safety in adults a single dose of 120 mg and the total daily dose of 150 mg has not been evaluated. In children and adolescents with a body weight up to 70 kg safety of single and total daily doses greater than 1.8 mg / kg is not known.
Aggressive behavior or hostility is often observed in children and adolescents with attention deficit hyperactivity disorder concentration. Communication aggressive behavior or hostility with taking Atomoxetine has not been established (they were observed in patients receiving the drug with no statistically significant differences when compared with the placebo group). During treatment, patients should be observed for signs of aggressive behavior or hostility.
During pregnancy, the drug is prescribed only if the potential benefit to the mother outweighs the potential risk to the fetus.
It is not known if atomoxetine is excreted in breast milk. It is necessary to refuse the appointment during breastfeeding.
The drug may be accompanied by sleepiness. In this regard, during the period of treatment should be taken when activities potentially hazardous activities that require high concentration and speed of psychomotor reactions (including driving).
National Register of Medicinal Products. Official publication: in 2 v. – M. Medical Council, 2009 – Volume 2, Part 1 – 568 p .; Part 2 -. 560