Duloxetine hydrochloride is a serotonin-norepinephrine reuptake inhibitor (SNRI) used to treat major depression, anxiety, and neuropathic pain. It may also be used for fibromyalgia, chronic musculoskeletal pain, chronic fatigue syndrome, and urinary incontinence.
Duloxetine hydrochloride is used to treat a variety of mental health conditions, such as, depression, anxiety, neuropathic pain, fibromyalgia, chronic musculoskeletal pain, chronic fatigue syndrome, and urinary incontinence.
| Brand Name | Duzela |
|---|---|
| Type | Capsule (Delayed Release) |
| Weight | 20 mg |
| Generic | Duloxetine Hydrochloride |
| Manufacturer | Sun Pharmaceutical Ltd. |
| Available in | English বাংলা |
Duzela Capsule (Delayed Release) 20 mg works by blocking the reuptake of serotonin and norepinephrine in the brain, resulting in an increased availability of these neurotransmitters and increased overall activity in the brain. This increases mood and reduces pain.
The effects of Duzela Capsule (Delayed Release) 20 mg can usually be felt within 1 to 2 weeks of starting treatment. However, the full therapeutic effect may not be seen for up to several weeks of treatment, depending on the severity of the condition being treated.
Duloxetine hydrochloride is well absorbed in the gastrointestinal tract, with peak concentrations reached in 1-2 hours. It is extensively metabolized in the liver and has a bioavailability of about 50%.
Duloxetine hydrochloride is metabolized in the liver and excreted in the feces and urine. Approximately 40% of the dose is excreted unchanged in the urine.
Duloxetine hydrochloride is available in 10 mg, 20 mg, 30 mg, and 60 mg capsules. The recommended starting dose is 30 to 60 mg per day, taken orally in divided doses once or twice daily. The dosage may be increased gradually, as needed, up to 120 mg per day.
Duloxetine hydrochloride should be taken orally in divided doses once or twice daily, with or without food. It may be taken with or without food, but it is important to take it consistently, either always with food or always without food.
Common side effects of duloxetine hydrochloride include nausea, constipation, dry mouth, loss of appetite, tremor, drowsiness, increased sweating, anxiety, and headaches.
Duloxetine hydrochloride is generally well tolerated, but overdosage may result in serotonin syndrome. Symptoms of serotonin syndrome include agitation, coma, muscle twitching, hallucinations, confusion, rapid heart rate, and high blood pressure.
Duloxetine hydrochloride should be used cautiously in patients with conditions that may be worsened by increases in serotonin levels, such as bipolar disorder, seizure disorders, or those taking monoamine oxidase inhibitors (MAOIs). It should also be used cautiously in elderly patients and in patients with renal or hepatic impairment. Patients should inform their healthcare provider if they are pregnant, planning to become pregnant, or breastfeeding.
Duloxetine hydrochloride may interact with a variety of medications, including antidepressants, certain pain medications, and antipsychotics. It can also interact with drugs that affect serotonin levels in the body, such as MAOIs and selective serotonin reuptake inhibitors (SSRIs). Patients should inform their healthcare provider of all medications they are taking prior to starting duloxetine hydrochloride.
Duloxetine hydrochloride should be used cautiously in patients with conditions that may be worsened by increases in serotonin levels, such as bipolar disorder and seizure disorders. It should also be used with caution in elderly patients, in patients with renal or hepatic impairment, and in those taking MAOIs.
Duloxetine hydrochloride can interact with a variety of medications, including antidepressants, certain pain medications, and antipsychotics. It can also interact with drugs that affect serotonin levels in the body, such as MAOIs and SSRIs.
Duloxetine hydrochloride should be taken consistently, either with or without food. It should not be taken with grapefruit juice, as this can increase the levels of the drug in the body.
Duloxetine hydrochloride is not recommended for use in pregnant women. If you are pregnant or planning to become pregnant, you should inform your healthcare provider prior to starting treatment with duloxetine hydrochloride.
Duloxetine hydrochloride is excreted in breast milk in very small amounts and is not recommended for use in breastfeeding women.
An acute overdose of duloxetine hydrochloride is likely to lead to symptoms of serotonin syndrome, such as agitation, confusion, rapid heart rate, and high blood pressure. Treatment of an acute overdose of duloxetine hydrochloride may include supportive measures, such as monitoring of vital signs and fluid balance, as well as gastric decontamination.
Duloxetine hydrochloride is contraindicated in patients with a known hypersensitivity to the drug and in those taking MAOIs.
Duloxetine hydrochloride should be taken orally in divided doses once or twice daily, with or without food. The recommended starting dose is 30 to 60 mg per day, taken orally in divided doses once or twice daily. The dosage may be increased gradually, as needed, up to 120 mg per day.
Duloxetine hydrochloride should be stored at room temperature, away from light and moisture, and in a tightly closed container.
Duloxetine hydrochloride has a volume of distribution of 8.3 to 16 liters.
The half-life of duloxetine hydrochloride is 11 to 14 hours.
Duloxetine hydrochloride has a clearance rate of 0.6 to 4.3 l/hr/kg.
See in details version Duzela Capsule (Delayed Release) 20 mg also Duzela Capsule (Delayed Release) 20 mg in bangla
Prof. Dr. Sehelly Jahan
Neurology (Brain, Nerve, Headache, Migraine) Specialist
Neurology Doctor in Dhaka