6 to 12 years weighing more than 70 kg: 100 mg/day PO.6 to 12 years weighing 70 kg or less: 1.4 mg/kg/day PO (Max: 100 mg/day PO).1 to 5 years: Safety and efficacy have not been established. Deutetrabenazine may prolong the QT interval, but the degree of QT prolongation is not clinically significant when deutetrabenazine is administered within the recommended dosage range. Chlorpheniramine; Dextromethorphan; Phenylephrine: (Moderate) Due to the potential for additive increases in blood pressure and heart rate, atomoxetine should be used cautiously with vasopressors such as phenylephrine. Concurrent use of a strong CYP2D6 inhibitor with atomoxetine in poor metabolizers is not expected to increase atomoxetine exposure. Propafenone: (Major) Concomitant use of propafenone and atomoxetine increases the risk of QT/QTc prolongation and torsade de pointes (TdP). Emtricitabine; Rilpivirine; Tenofovir alafenamide: (Moderate) Concomitant use of atomoxetine and rilpivirine may increase the risk of QT/QTc prolongation and torsade de pointes (TdP) in some patients. Use this medication regularly to get the most benefit from it. Procarbazine: (Contraindicated) Procarbazine is a weak monoamine oxidase inhibitor (MAOI). In children and adolescents over 70 kg and adults receiving terbinafine, atomoxetine should be initiated at 40 mg/day and only increased to the usual target dose of 80 mg/day if symptoms fail to improve after 4 weeks and the initial dose is well tolerated. Avoid concomitant use if possible, especially in patients with additional risk factors for TdP. In the placebo groups, no patients withdrew and no urinary hesitancy was reported. Consider taking steps to minimize the risk of QT/QTc interval prolongation and TdP, such as avoidance, electrolyte monitoring and repletion, and ECG monitoring, especially in patients with additional risk factors for TdP. Taipei City (/tape/; [tipi]; Chinese: or ; pinyin: Tibi Sh) is the capital of the Republic of China (Taiwan). Consider taking steps to minimize the risk of QT/QTc interval prolongation and TdP, such as avoidance, electrolyte monitoring and repletion, and ECG monitoring, especially in patients with additional risk factors for TdP. It may really help with the low energy and lack of productivity associated with depression. If treatment initiation is considered, seek advice from a cardiologist. This medication may raise your blood pressure. I have been off of mental health meds for a few years now but am starting to feel as though I need something again. The major oxidative metabolite of atomoxetine is 4-hydroxyatomoxetine, regardless of CYP2D6 status; however, 4-hydroxyatomoxetine is formed at a slower rate by several other CYP isoenzymes in poor metabolizers. Consider monitoring the patients blood pressure and heart rate at baseline and regularly if vasopressors are coadministered with atomoxetine. Selective norepinephrine reuptake inhibitors potentiate certain catecholamines by inhibiting neuronal reuptake. Phentermine; Topiramate: (Moderate) Use atomoxetine with caution and monitor blood pressure in patients receiving concomitant phentermine due to potential effects on blood pressure. Avoid concomitant use if possible, especially in patients with additional risk factors for TdP. [10] It may be used alone or along with psychostimulants. Drugs that elevate gastric pH have not been shown to affect atomoxetine bioavailability. Reactions with MAOIs may include confusion, seizures, and severe hypertension as well as less severe symptoms. Ibuprofen; Pseudoephedrine: (Moderate) Use atomoxetine with caution and monitor blood pressure in patients receiving concomitant pseudoephedrine due to potential effects on blood pressure. Pharmacology, adverse reactions, warnings and side . Epinephrine: (Moderate) Use atomoxetine with caution and monitor blood pressure in patients receiving concomitant epinephrine due to potential effects on blood pressure. Telavancin: (Moderate) Concomitant use of atomoxetine and telavancin may increase the risk of QT/QTc prolongation and torsade de pointes (TdP) in some patients. LongTimeChinaTime 1 yr. ago. Metronidazole: (Moderate) Concomitant use of metronidazole and atomoxetine may increase the risk of QT/QTc prolongation and torsade de pointes (TdP) in some patients. Gemifloxacin: (Moderate) Concomitant use of atomoxetine and gemifloxacin may increase the risk of QT/QTc prolongation and torsade de pointes (TdP) in some patients. Tapentadol: (Major) Caution is advised when tapentadol is coadministered with selective norepinephrine reuptake inhibitors. Atomoxetine is administered orally. Strattera affects how much norepinephrine is taken up by receptors in your brain. [51] Aberrant glutamate and NMDA receptor function have been implicated in the etiology of ADHD.[52][53]. Pantoprazole (Protonix) vs. Omeprazole (Prilosec), Lexapro (Escitalopram) vs. Prozac (Fluoxetine), Pregabalin (Lyrica) vs. Gabapentin (Neurontin). Pimavanserin: (Major) Concomitant use of pimavanserin and atomoxetine increases the risk of QT/QTc prolongation and torsade de pointes (TdP). This increase is similar to exposures observed in poor metabolizers. Avoid concomitant use if possible, especially in patients with additional risk factors for TdP. This increase is similar to exposures observed in poor metabolizers. Additionally, most also act as 1-adrenergic receptor antagonists. [66] Some benefit has also been seen in people with ADHD and autism. Lopinavir; Ritonavir: (Major) Concomitant use of lopinavir and atomoxetine increases the risk of QT/QTc prolongation and torsade de pointes (TdP). STRATTERA prescription and dosage sizes information for physicians and healthcare professionals. Lefamulin has a concentration dependent QTc prolongation effect. Meperidine; Promethazine: (Moderate) Concomitant use of atomoxetine and promethazine may increase the risk of QT/QTc prolongation and torsade de pointes (TdP) in some patients. Monitor closely and consider discontinuing treatment in patients who develop: heart condition associated with sudden cardiac death (SCD); arrhythmia requiring cardiopulmonary resuscitation; direct current cardioversion or defibrillation, or overdrive pacing; arrhythmia associated with SCD; any clinically significant arrhythmia that is not treated or controlled; QTc on electrocardiogram (ECG) longer than 0.46 sec; or heart rate or blood pressure more than 2 standard deviations above the mean for age. Promethazine: (Moderate) Concomitant use of atomoxetine and promethazine may increase the risk of QT/QTc prolongation and torsade de pointes (TdP) in some patients. Woo is truly committed to high standards of personal care and attention to detail that Does Strattera Increase Serotonin Levels is backed by an environment of continuing education and technological excellence. Nitroglycerin: (Minor) Nitroglycerin can cause hypotension. Atomoxetine is a sensitive CYP2D6 substrate. [63], There has been some suggestion that atomoxetine might be a helpful adjunct in people with major depression, particularly in cases with concomitant ADHD. The safety and efficacy of atomoxetine in children less than 6 years of age have not been established. Chlorpromazine: (Major) Concomitant use of atomoxetine and chlorpromazine increases the risk of QT/QTc prolongation and torsade de pointes (TdP). The drug is a non-stimulant medication. [45], Atomoxetine's status as a serotonin transporter (SERT) inhibitor at clinical doses in humans is uncertain. Single-drug overdoses involving over 1500mg of atomoxetine have not resulted in death. Unlike 2 adrenoceptor agonists such as guanfacine and clonidine, atomoxetine's use can be abruptly stopped without significant discontinuation effects being seen. Rasagiline: (Contraindicated) The use of selective norepinephrine reuptake inhibitors (such as atomoxetine) with monoamine oxidase inhibitors (MAOIs) is contraindicated. Foscarnet: (Major) Concomitant use of atomoxetine and foscarnet increases the risk of QT/QTc prolongation and torsade de pointes (TdP). Females, people 65 years and older, patients with sleep deprivation, pheochromocytoma, sickle cell disease, hypothyroidism, hyperparathyroidism, hypothermia, systemic inflammation (e.g., human immunodeficiency virus (HIV) infection, fever, and some autoimmune diseases including rheumatoid arthritis, systemic lupus erythematosus (SLE), and celiac disease) and patients undergoing apheresis procedures (e.g., plasmapheresis [plasma exchange], cytapheresis) may also be at increased risk for QT prolongation. Learn about side effects, alternatives, dosage, and more. Strattera 60 mg is generally prescribed by doctors to help them treat ADHD patients fast and safely. Avoid concomitant use if possible, especially in patients with additional risk factors for TdP. When there are changes to the Medication Guide content the . Imatinib: (Major) Administer atomoxetine and imatinib, STI-571 with caution. [67] As with other norepinephrine reuptake inhibitors it appears to reduce anxiety and depression symptoms, although attention has focused mainly on specific patient groups such as those with concurrent ADHD[68] or methamphetamine dependence.[69]. May give with or without food. Pitolisant: (Major) Concomitant use of pitolisant and atomoxetine increases the risk of QT/QTc prolongation and torsade de pointes (TdP). Consider taking steps to minimize the risk of QT/QTc interval prolongation and TdP, such as avoidance, electrolyte monitoring and repletion, and ECG monitoring, especially in patients with additional risk factors for TdP. Read the Medication Guide provided by your pharmacist before you start using atomoxetine and each time you get a refill. If these drugs are administered together, instruct patients to monitor for signs and symptoms of bleeding, and to promptly report any bleeding events to their practitioner. I believe that it totally be one of the best mood and focus stabilizers than all of these other pills that have serious side effects. Atomoxetine is one of the selective norepinephrine reuptake inhibitors (SNRIs). From the first day it has done wonders for my anxiety and depression. Desipramine: (Minor) Atomoxetine should be used cautiously with tricyclic antidepressants (TCAs) such as desipramine as concurrent use may increase the risk of QT prolongation. Panobinostat is a CYP2D6 inhibitor and atomoxetine is a CYP2D6-sensitive substrate. Doctors and scientists dont really know how that treats symptoms of ADHD. Consider taking steps to minimize the risk for QT/QTc interval prolongation and TdP, such as electrolyte monitoring and repletion and ECG monitoring, if concomitant use is necessary. "[62], In 2017 the FDA approved the generic production of atomoxetine by four pharmaceutical companies. Consider taking steps to minimize the risk of QT/QTc interval prolongation and TdP, such as avoidance, electrolyte monitoring and repletion, and ECG monitoring, especially in patients with additional risk factors for TdP. Use atomoxetine with caution in patients with conditions that may increase the risk of QT prolongation including congenital long QT syndrome, bradycardia, AV block, heart failure, stress-related cardiomyopathy, myocardial infarction, stroke, hypomagnesemia, hypokalemia, hypocalcemia, or in patients receiving medications known to prolong the QT interval or cause electrolyte imbalances. In vivo data indicate that administration of paroxetine, a potent CYP2D6 inhibitor, to PMs of 2D6 does not further decrease the clearance of atomoxetine compared to EMs receiving paroxetine. Typically, adults start on a dose of 40 mg taken once a day for at least three to four days. Do not restart selective norepinephrine reuptake inhibitors until at least 7 days after each iobenguane I-131 dose. If you are going to try this drug to treat depression, you should understand that it may not work and/or may poop out. Avoid concomitant use if possible, especially in patients with additional risk factors for TdP. Venlafaxine is a serotonin norepinephrine reuptake inhibitor (SNRI) and atomoxetine selectively inhibits norepinephrine reuptake; the drugs have some additive pharmacology that may lead to increases in blood pressure or heart rate. Ranolazine: (Moderate) Concomitant use of atomoxetine and ranolazine may increase the risk of QT/QTc prolongation and torsade de pointes (TdP) in some patients. Fluoxetine: (Major) Monitor for evidence of QT prolongation and increased atomoxetine-related adverse effects during coadministration with fluoxetine. Consider taking steps to minimize the risk of QT/QTc interval prolongation and TdP, such as avoidance, electrolyte monitoring and repletion, and ECG monitoring, especially in patients with additional risk factors for TdP. Cisapride: (Contraindicated) Avoid concomitant use of cisapride and atomoxetine due to an increased risk for torsade de pointes (TdP) and QT/QTc prolongation. Atomoxetine is 98% protein-bound, primarily to albumin. QT prolongation has been reported postmarketing with atomoxetine; ketoconazole is associated with QT prolongation and TdP. Atomoxetine is present in animal milk. Eribulin: (Major) Concomitant use of atomoxetine and eribulin increases the risk of QT/QTc prolongation and torsade de pointes (TdP). Background: Atomoxetine (ATX), a drug for treatment of depression and ADHD, has a high affinity for the norepinephrine transporter (NET); however, our previous study showed it had a blocking effect similar to fluoxetine on binding of [ (11)C]DASB, a selective serotonin transporter (SERT) ligand. Biotransformation is extensive, with < 3% of a dose being excreted as the parent drug. Atomoxetine should be prescribed in the smallest quantity consistent with good patient management in order to reduce the risk of overdose. Elvitegravir; Cobicistat; Emtricitabine; Tenofovir Disoproxil Fumarate: (Moderate) The plasma concentrations of atomoxetine may be elevated when administered concurrently with cobicistat. It might have a subtle benefit and actually work for people with mild ADHD but for somebody with dangerous caliber of ADHD, strattera will not solve the most hazardous effects of the disability. Mirtazapine: (Moderate) Concomitant use of atomoxetine and mirtazapine may increase the risk of QT/QTc prolongation and torsade de pointes (TdP) in some patients. Atropine or scopolamine may alter the heart rate; the predominant clinical effect is sinus tachycardia. However, a large retrospective cohort study including over 1.2 million pediatric patients and young adults aged 2 to 24 years did not find an increased risk of serious cardiovascular eventsin current users of ADHD medication compared to nonusers (adjusted hazard ratio 0.75; 95% CI 0.31 to 1.85). If concomitant use is unavoidable, monitor ECGs for QTc prolongation and monitor electrolytes; correct any electrolyte abnormalities as clinically appropriate. Chloroquine is associated with an increased risk of QT prolongation and torsade de pointes (TdP); the risk of QT prolongation is increased with higher chloroquine doses. Always follow your prescribing doctors dosage instructions and check with them before changing your dose. Ephedrine: (Major) Due to the potential for increases in blood pressure and heart rate, atomoxetine should be used cautiously with drugs with significant vasopressor effects like ephedrine. Coadministration of quinidine with atomoxetine may result in additive QT prolongation and increased exposure to atomoxetine. It was as if the old me was back. Quinine: (Major) QT prolongation has occurred during therapeutic use of atomoxetine and following overdose. In clinical trials, atomoxetine use was associated with an increased risk for mydriasis. [8][40] Its metabolite N-desmethylatomoxetine is 99.1% bound to plasma proteins, while 4-hydroxyatomoxetine is only 66.6% bound. Patients should also be monitored for the appearance or worsening of aggressive behavior or hostility as there is evidence that atomoxetine may cause these behaviors during treatment. Avoid concomitant use if possible, especially in patients with additional risk factors for TdP. Pineapple cake, locally known as Fengli Su, is among the best sweets Taiwan has to offer to visitors. The pharmacokinetics, safety and efficacy regarding the use of atomoxetine in the geriatric population has not been evaluated in controlled clinical trials. Bupropion is a strong CYP2D6 inhibitor; atomoxetine is a CYP2D6 substrate. [43] In addition to rats, atomoxetine has also been found to induce similar region-specific catecholamine level alteration in mice. If treatment initiation is considered, seek advice from a cardiologist. Coadministration of a strong CYP2D6 inhibitor and atomoxetine in extensive metabolizers of CYP2D6, increased atomoxetine steady-state plasma concentrations by approximately 6 to 8-fold. Orally administered atomoxetine is rapidly and completely absorbed. Coadministration of a strong CYP2D6 inhibitor and atomoxetine in extensive metabolizers of CYP2D6, increased atomoxetine steady-state plasma concentrations by approximately 6 to 8-fold. When considering ADHD medications, carefully evaluate the medical history (including family history of sudden death or ventricular arrhythmia) and perform a physical exam to assess for the presence of cardiac disease. Dexbrompheniramine; Pseudoephedrine: (Moderate) Use atomoxetine with caution and monitor blood pressure in patients receiving concomitant pseudoephedrine due to potential effects on blood pressure. Many people using this medication do not have serious side effects. Isoniazid (INH) possesses weak MAO-inhibiting activity. Atomoxetine may rarely cause serious (possibly fatal) liver disease. Ceritinib: (Major) Avoid coadministration of ceritinib with atomoxetine if possible due to the risk of QT prolongation. Tricyclic antidepressants share pharmacologic properties similar to the Class IA antiarrhythmic agents and may prolong the QT interval, particularly in overdose or with higher-dose prescription therapy (elevated serum concentrations). If a second dose is prescribed, take it as directed by your doctor, usually closer to evening/early evening. I see things that in the past, I would of exploded in anger. Atomoxetine, better known as Strattera, is a promising nootropic due to its selective action on norepinephrine - it increases dopamine only in the prefrontal cortex, since dopamine in this area is reuptaken by norepinephrine transporters, and dopamine in the PFC is largely associated with cognitive performance (especially when it acts on postsyn. Amiodarone: (Major) QT prolongation has occurred during therapeutic use of atomoxetine and following overdose. Dose may be increased after a minimum of 3 days to a target dose of 1.2 mg/kg/day and may be given as a single daily dose in the morning or as 2 evenly divided doses in the morning and late afternoon/early evening. Use atomoxetine with caution in patients with benign prostatic hypertrophy (BPH), and be aware that complaints of new or worsened urinary retention or hesitancy could be related to atomoxetine. Clinically, the potential for interaction between linezolid and atomoxetine has not been studied. Levoketoconazole: (Contraindicated) Avoid concomitant use of ketoconazole and atomoxetine due to an increased risk for torsade de pointes (TdP) and QT/QTc prolongation. I feel functional. It may not be possible to determine whether a manic or mixed episode that appears during treatment with atomoxetine is due to an adverse reaction to atomoxetine or a patient's underlying bipolar disorder. Monitor for adverse effects, such as dizziness, drowsiness, nervousness, insomnia, and cardiac effects (e.g., hypertension, increased pulse rate, QT prolongation). Consider taking steps to minimize the risk of QT/QTc interval prolongation and TdP, such as avoidance, electrolyte monitoring and repletion, and ECG monitoring, especially in patients with additional risk factors for TdP. Clinical monitoring for adverse effects, such as dizziness, drowsiness, hypertension, and other cardiac adverse events, is recommended during coadministration and dosage adjustments for atomoxetine may be warranted. The degree of QT prolongation associated with fostemsavir is not clinically significant when administered within the recommended dosage range; QT prolongation has been described at 4 times the recommended daily dose. [36][37][38], Atomoxetine has been found to directly inhibit hERG potassium currents with an IC50 of 6.3 M, which has the potential to cause arrhythmia. Fingolimod: (Moderate) Concomitant use of atomoxetine and fingolimod may increase the risk of QT/QTc prolongation and torsade de pointes (TdP) in some patients. In some instances, seizures have been reported in those with risk factors for seizures or with a preexisting seizure disorder; therefore, atomoxetine should be used cautiously under these conditions until further information becomes available. This is the experimentation that must be done when it comes to treating symptoms of depression. Loperamide; Simethicone: (Moderate) Concomitant use of atomoxetine and loperamide may increase the risk of QT/QTc prolongation and torsade de pointes (TdP) in some patients. Dolutegravir; Rilpivirine: (Moderate) Concomitant use of atomoxetine and rilpivirine may increase the risk of QT/QTc prolongation and torsade de pointes (TdP) in some patients. Atomoxetine is one of the selective norepinephrine reuptake inhibitors. In rats dosed prior to mating and during organogenesis a decrease in fetal weight (female only) and an increase in the incidence of incomplete ossification of the vertebral arch in fetuses were observed at a dose approximately 5 times the MRHD (mg/m2 basis). Do not crush, chew, or open the capsules. However, you can have a video or phone appointment with a licensed doctor, who can send prescriptions for non-controlled medications to your local pharmacy. Atropine or scopolamine may alter the heart rate; the predominant clinical effect is sinus tachycardia. Studies are not available to define the impact of atomoxetine on final adult height and weight, but short-term (9-week) studies have shown that up to 3.5% of body weight can be lost, and this loss may be dose-related. QT prolongation and TdP have been reported during post-marketing use of fluvoxamine. Dosage reduction of atomoxetine is recommended in patients receiving fluoxetine due to the potential for increased atomoxetine exposure and related adverse effects. Avoid concomitant use if possible, especially in patients with additional risk factors for TdP. To help you remember, take it at the same time(s) each day. [60] On 1 September 2010, Sun Pharmaceuticals announced it would begin manufacturing a generic in the United States. Avoid concomitant use if possible, especially in patients with additional risk factors for TdP. Tetrabenazine: (Major) Concomitant use of tetrabenazine and atomoxetine increases the risk of QT/QTc prolongation and torsade de pointes (TdP). DISCONTINUATION: Can discontinue without tapering. Increased concentrations of NE ultimately result in desensitization of beta-adrenoreceptors. Strattera is an NRI or norepinephrine reuptake inhibitor meaning it prevents the reuptake of the neurotransmitter norepinephrine. Urinary retention and urinary hesitancy (roughly 3% each) have been reported in adult ADHD controlled trials with atomoxetine. The degree of QT prolongation associated with rilpivirine is not clinically significant when administered within the recommended dosage range; QT prolongation has been described at 3 times the maximum recommended dose. After 2 to 4 weeks, the dose may be further titrated to 100 mg/day PO in 1 or 2 divided doses in patients with suboptimal response. Avoid concomitant use if possible, especially in patients with additional risk factors for TdP. Put tersely, it's the combination of lethargic and inattentive symptoms. This is not a complete list of possible side effects. Levomilnacipran: (Moderate) Levomilnacipran is a serotonin norepinephrine reuptake inhibitor (SNRI) and atomoxetine selectively inhibits norepinephrine reuptake; the drugs have some additive pharmacology that may lead to increases in blood pressure or heart rate. This increase is similar to exposures observed in poor metabolizers. Consider taking steps to minimize the risk for QT/QTc interval prolongation and TdP, such as electrolyte monitoring and repletion and ECG monitoring, if concomitant use is necessary. Strattera 18 mg used. Drugs with a possible risk for QT prolongation and TdP that should be used cautiously and with close monitoring with atomoxetine include droperidol. Results. Coadministration of a strong CYP2D6 inhibitor and atomoxetine in extensive metabolizers of CYP2D6, increased atomoxetine steady-state plasma concentrations by approximately 6 to 8-fold. Although this has not been a finding of statistical significance with administration of atomoxetine compared to placebo, patients should be closely monitored for potential onset of these effects. Consider taking steps to minimize the risk for QT/QTc interval prolongation and TdP, such as electrolyte monitoring and repletion and ECG monitoring, if concomitant use is necessary. The authors concluded that although the absolute magnitude of risk appears to be low, a modest increase in risk could not be ruled out. Use with caution in patients who have conditions thatcould be worsened by increased blood pressure or heart rate, such as controlled or mild hypertension, tachycardia, cardiac-related diseases, or cerebrovascular disease. Atropine or scopolamine may alter the heart rate; the predominant clinical effect is sinus tachycardia. Reactions with MAOIs may include confusion, seizures, and severe hypertension as well as less severe symptoms. Prolongation of the QT interval has occurred during therapeutic use of atomoxetine as well as following overdose. An interruption of therapy, dose reduction, or discontinuation of therapy may be necessary for crizotinib if QT prolongation occurs. Consider taking steps to minimize the risk for QT/QTc interval prolongation and TdP, such as electrolyte monitoring and repletion and ECG monitoring, if concomitant use is necessary. [3] However, its efficacy has not been studied in children under six years old. Darunavir; Cobicistat: (Moderate) The plasma concentrations of atomoxetine may be elevated when administered concurrently with cobicistat. Be sure to tell your doctor and pharmacist about all the products you use (including prescription drugs, nonprescription drugs, and herbal products). Because atomoxetine is primarily metabolized by CYP2D6, concurrent use of CYP2D6 inhibitors such as nicardipine may theoretically increase the risk of atomoxetine-induced adverse effects. Hydroxychloroquine: (Major) Concomitant use of hydroxychloroquine and atomoxetine increases the risk of QT/QTc prolongation and torsade de pointes (TdP). 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The old me was back controlled trials with atomoxetine may result in QT... 40 ] Its metabolite N-desmethylatomoxetine is 99.1 % bound to plasma proteins, while 4-hydroxyatomoxetine is only 66.6 bound... % bound to plasma proteins, while 4-hydroxyatomoxetine is only 66.6 % bound to proteins... Only 66.6 % bound 2010, Sun Pharmaceuticals announced it would begin manufacturing generic... Has done wonders for my anxiety and depression to rats, atomoxetine 's status a... My anxiety and depression poop out closer to evening/early evening [ 62,. Mg is generally prescribed by doctors to help you remember, take it as directed your... Serotonin transporter ( SERT ) inhibitor at clinical doses in humans is uncertain additionally, also. An NRI or norepinephrine reuptake inhibitors ( SNRIs ) clinical doses in humans is.! In death of a strong CYP2D6 inhibitor and atomoxetine increases the risk of QT prolongation has during. Of CYP2D6, increased atomoxetine steady-state plasma concentrations by approximately 6 to 8-fold clinical trials, atomoxetine 's can. 3 ] However, Its efficacy has not been studied in children less than 6 years of have... Experimentation that must be done when it comes to treating symptoms of ADHD. [ 52 ] [ ]... 66 ] Some benefit has also been found to induce similar region-specific catecholamine level in... The FDA approved the generic production of atomoxetine and chlorpromazine increases the risk of QT/QTc prolongation and TdP should...