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Ariclaim (Duloxetine)

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Ariclaim is a type of antidepressant known as a serotonin–norepinephrine reuptake inhibitor used to treat depression and anxiety. Ariclaim may improve your mood, sleep, appetite, and energy level, and decrease nervousness.

Other names for this medication:
Ariclaim, Combac, Delok, Deneurone, Detine, Dimorex, Dulex, Dulife, Dulojoy, Dulok, Dulomax, Dulonix, Dulot, Dulotin, Dulotrac, Duloxee, Duloxetine, Duloxit, Duloxyl, Dulti, Dumore, Duonex, Dureep, Dutin, Dutine, Duxet, Duzac, Duzela, Neuroxeti, Sylonex, Symbal, Sympta, Ulozet, Xeristar, Yentreve

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Also known as: Duloxetine


Ariclaim (duloxetine) is a selective serotonin and norepinephrine reuptake inhibitor antidepressant (SSNRI). Duloxetine affects chemicals in the brain that may be unbalanced in people with depression.

Ariclaim is used to treat major depressive disorder in adults. It is also used to treat general anxiety disorder in adults and children who are at least 7 years old.

Ariclaim is also used in adults to treat nerve pain caused by diabetes (diabetic neuropathy), or chronic muscle or joint pain (such as low back pain and osteoarthritis pain).

Ariclaim is also used to treat fibromyalgia (a chronic pain disorder) in adults and children at least 13 years old.


Usual Adult Dose for Depression:

Initial dose: 20 mg to 30 mg orally 2 times a day Maintenance dose: 60 mg per day, given either once a day OR 30 mg orally 2 times a day Maximum dose: 120 mg/day.

Usual Adult Dose for Fibromyalgia:

Initial dose: 30 mg orally once a day for at least 1 week Maintenance dose: 30 to 60 mg orally once a day.

Usual Adult Dose for Generalized Anxiety Disorder:

Initial dose: 60 mg orally once a day Maintenance dose: 60 to 120 mg orally once a day Maximum dose: 120 mg/day.

Usual Adult Dose for Pain:

Initial dose: 30 to 60 mg orally once a day Maintenance dose: 60 mg orally once a day.

Usual Adult Dose for Neuropathic Pain:

Initial dose: 30 to 60 mg orally once a day Maintenance dose: 60 mg orally once a day.

Usual Adult Dose for Chronic Pain:

Initial dose: 30 to 60 mg orally once a day Maintenance dose: 60 mg orally once a day.

Usual Geriatric Dose for Generalized Anxiety Disorder:

Initial dose: 30 mg orally once a day for at least 2 weeks Maintenance dose: 60 mg orally once a day Maximum dose: 120 mg/day.

Usual Pediatric Dose for Generalized Anxiety Disorder:

7 to 17 years: -Initial dose: 30 mg orally once a day for at least 2 weeks -Maintenance dose: 30 to 60 mg orally once a day -Maximum dose: 120 mg/day.

Usual Pediatric Dose for Fibromyalgia:

13 years and older: -Initial dose: 30 mg orally once a day for at least 1 week -Maintenance dose: 30 to 60 mg orally once a day.

Detailed Ariclaim dosage information


If you take an overdose of Ariclaim, you should seek emergency medical attention or contact your healthcare provider immediately.


Store at a room temperature between 4 and 30 degrees C (39 and 86 degrees F) away from moisture, light and heat. Throw away the after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Ariclaim 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.


Avoid driving or hazardous activity until you know how this medicine will affect you. Your reactions could be impaired. Dizziness or fainting can cause falls, accidents, or severe injuries.

Avoid getting up too fast from a sitting or lying position, or you may feel dizzy.

Drinking alcohol may increase your risk of liver damage, especially if you take Drizalma.

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To investigate the value of metalloproteinase glimepiride overdose -3 (MMP-3) levels in assessing efficacy of etanercept treatment in patients with ankylosing spondylitis (AS). Expression of HIV type 1 PR in Escherichia coli as a fusion protein gave rapid autocatalytic processing to an HIV-specific protein of approximately 11 kilodaltons. To examine whether cLBP affects VPAC performance during a loaded forward reach (LFR) task. Botulinum toxin injection was performed without anaesthesia following a specific protocol. To describe the microbiological and therapeutic characteristics of confirmed neonatal sepsis, and determineits incidence and mortality, at the National Hospital Arzobispo Loayza (HNAL) from 2011 to 2012, Lima, Peru. In vitro release modulation from crosslinked pellets for site-specific drug delivery to the gastrointestinal tract. The mechanistic details of CPAF action, however, remain obscure.

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