Duloxetine delayed-release capsules are indicated for the treatment of: Major depressive disorder in adults Generalized anxiety disorder in adults and pediatric patients 7 years of age and older Diabetic peripheral neuropathic pain in adults Fibromyalgia in adults and pediatric patients 13 years of age and older Chronic musculoskeletal pain in adults Duloxetine delayed-release capsules are a serotonin and norepinephrine reuptake inhibitor (SNRI) indicated for the treatment of the following conditions: Major depressive disorder (MDD) in adults Generalized anxiety disorder (GAD) in adults and pediatric patients 7 years of age and older Diabetic peripheral neuropathic pain (DPNP) in adults Fibromyalgia (FM) in adults and pediatric patients 13 years of age and older Chronic musculoskeletal pain in adults.
From the U.S. FDA-approved label for Duloxetine. Full label: DailyMed.
Duloxetine delayed-release capsules are indicated for the treatment of: Major depressive disorder in adults Generalized anxiety disorder in adults and pediatric patients 7 years of age and older Diabetic peripheral neuropathic pain in adults Fibromyalgia in adults and pediatric patients 13 years of age and older Chronic musculoskeletal pain in adults Duloxetine delayed-release capsules are a serotonin and norepinephrine reuptake inhibitor (SNRI) indicated for the treatment of the following conditions: Major depressive disorder (MDD) in adults Generalized anxiety disorder (GAD) in adults and pediatric patients 7 years of age and older Diabetic peripheral neuropathic pain (DPNP) in adults Fibromyalgia (FM) in adults and pediatric patients 13 years of age and older Chronic musculoskeletal pain in adults.
From the U.S. FDA-approved label for Duloxetine. Full label: DailyMed.
Take duloxetine delayed-release capsules once daily, with or without food.
Directions from the U.S. FDA-approved label for Duloxetine — your doctor or pharmacist may advise differently.
The use of MAOIs intended to treat psychiatric disorders with duloxetine or within 5 days of stopping treatment with duloxetine is contraindicated because of an increased risk of serotonin syndrome. The use of duloxetine within 14 days of stopping an MAOI intended to treat psychiatric disorders is contraindicated. Starting duloxetine in a patient who is being treated with MAOIs such as linezolid or intravenous methylene blue is also contraindicated because of an increased risk of serotonin syndrome.
Excerpt from the U.S. FDA-approved label for Duloxetine. Talk to a pharmacist or doctor before use.
Hepatotoxicity: Hepatic failure, sometimes fatal, has been reported. Discontinue duloxetine in patients who develop jaundice or other evidence of clinically significant liver dysfunction and should not be resumed unless another cause can be established. Avoid use in patients with substantial alcohol use or evidence of chronic liver disease Orthostatic Hypotension, Falls and Syncope: Consider dosage reduction or discontinuation if these events occur Serotonin Syndrome: Increased risk when co-administered with other serotonergic agents but also when taken alone.
Warnings and precautions excerpt from the U.S. FDA-approved label for Duloxetine — not a complete list. Talk to a pharmacist or doctor before use.
The following serious adverse reactions are described below and elsewhere in the labeling: Suicidal Thoughts and Behaviors in Children, Adolescents and Young Adults Hepatotoxicity Orthostatic Hypotension, Falls and Syncope Serotonin Syndrome Increased Risk of Bleeding Severe Skin Reactions Discontinuation Syndrome Activation of Mania/Hypomania Angle-Closure Glaucoma Seizures Increases in Blood Pressure Clinically Important…
Excerpt from the U.S. FDA-approved label for Duloxetine — not a complete list. Talk to a pharmacist or doctor about side effects.
20 brands · 7 makers in the NepalDoc catalog — see the full Duloxetine guide →
Store at 25°C (77°F);
Storage information from the U.S. FDA-approved label for Duloxetine.
What is Dulot 20?
Dulot 20mg Tablet is a Duloxetine medicine made by Magnus Pharma Pvt. Ltd. It comes as 20mg Tablet.
What is the generic name of Dulot 20?
The generic name of Dulot 20 is Duloxetine.
Which brands of Duloxetine are available in Nepal?
20 brands of Duloxetine are listed in the NepalDoc catalog, from 7 makers — including Dulane 30mg Tablet, Duletin 20mg Tablet, Duletin 30mg Tablet, Dulot 30mg Tablet, Dulot 40mg Tablet, Duloxit 20mg Tablet.
What are the side effects of Duloxetine?
The following serious adverse reactions are described below and elsewhere in the labeling: Suicidal Thoughts and Behaviors in Children, Adolescents and Young Adults Hepatotoxicity Orthostatic Hypotension, Falls and Syncope Serotonin Syndrome Increased Risk of Bleeding Severe Skin Reactions Discontinuation Syndrome Activation of Mania/Hypomania Angle-Closure Glaucoma Seizures Increases in Blood Pressure Clinically Important…
This page is information only and is not medical advice. Medicine details come from the sources listed above and may change — always confirm the medicine, strength and dose with a pharmacist or doctor before use. A catalog listing does not guarantee that a medicine is in stock at any pharmacy.
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