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Cymbalta vs effexor for anxiety

Cymbalta vs effexor for anxiety

Cymbalta

SNRIs increase serotonin and norepinephrine levels. The amygdala and the hippocampus are also affected by norepinephrine, which is a neurotransmitter used by a number of neural systems. Norepinephrine also has an impact on the thalamus and prefrontal cortex, according to research. 3 It also controls the body’s mechanisms that control heart rate, breathing, and blood flow to the muscles.
Aspirin serves as a convenient analogy.
1 Consider a tooth that has been cracked by hard candy and has developed an abscess. You develop a toothache and a low-grade fever as a result. It would be incorrect to conclude that your problems were caused by a lack of aspirin in your system if you take aspirin and your toothache and fever vanish.
SNRIs have more side effects than SSRIs because they target norepinephrine receptors as well as serotonin receptors. Any potential side effects that you are experiencing should be discussed with your doctor. Different drugs have different effects on you, so you can need to try a few before finding one with less side effects.

2-minute neuroscience: serotonin-norepinephrine reuptake

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Antidepressants administered by a doctor are a common treatment choice for panic disorder, since they can help alleviate the effects of panic attacks and anxiety. Antidepressants like Cymbalta (duloxetine) are commonly prescribed by people who have been diagnosed with panic disorder. Cymbalta will help ease depressive symptoms if you’ve been diagnosed with it because it’s an antidepressant. Cymbalta belongs to the serotonin and norepinephrine reuptake inhibitors class of antidepressants (SNRIs). SNRIs were discovered to be an effective cure for anxiety disorders such as panic disorder, generalized anxiety disorder (GAD), particular phobias, and social anxiety disorder (SAD), as well as agoraphobia. They were originally used to treat mood disorders such as depression and bipolar disorder.

Cymbalta (duloxetine): what are the side effects? watch

Separate evaluations of effectiveness (benefit) and adverse events are common in clinical trials evaluating antidepressant therapies (risk). The global benefit-risk (GBR) evaluation enables both effectiveness and adverse events to be measured at the same time. The goal was to use GBR research to compare the serotonin and norepinephrine reuptake inhibitors (SNRIs) duloxetine and venlafaxine.
There were no substantial variations in GBR scores between duloxetine 60 mg/day and venlafaxine 150 mg/day at the end of 6 weeks (-1.418 vs. -1.079, P = 0.217) or 12 weeks (-0.349 vs. -0.121, P = 0.440), nor were there significant differences in the majority of efficacy tests. In contrast to duloxetine-treated patients (64.8 percent, P =.006), substantially more venlafaxine-treated patients (74.5 percent) completed 12 weeks of treatment. During the first 6 weeks of therapy, nausea was the most frequent treatment-emergent adverse effect (TEAE) for both medications, and it was substantially higher for duloxetine 60 mg/day compared to venlafaxine 150 mg/day (43.6 percent vs. 35.0 percent , P0.05). During the taper phase, venlafaxine-treated patients registered substantially more discontinuation-emergent adverse effects (DEAEs) than patients on duloxetine. During the fixed dosing duration, venlafaxine-treated patients (n = 4) had significantly more prolonged elevations of systolic blood pressure (n=0, P =.047) than duloxetine-treated patients (n=0, P =.047). During 6 and 12 weeks of counseling, there were few major variations in safety measures between treatment classes.

All about serotonin & norepinephrine reuptake inhibitors

Depression is a crippling mental illness that affects people all over the world. There are a variety of antidepressants used to treat a variety of depressive disorders. So, which are the most important for treating particular forms of depression? IMS Health has compiled a list of the top 100 most commonly prescribed medications. On the overall chart, some of the antidepressants on this list were very strong. Cymbalta, for example, was three times more often prescribed than the second most commonly prescribed antidepressant.
It’s important to remember that antidepressants alter the chemical makeup of the brain. Depression is handled in this manner. Antidepressants can be abused, resulting in a co-occurring illness. Prescription drug misuse is more common in people with some mood disorders. Antidepressant drugs do not have the same addictive properties as opioids or alcohol. While there are less cravings, there is a chance of physical dependency. It also increases the risk of other medications being abused.