NeuroStar® TMS Therapy
FDA-cleared, non-medication depression treatment
(855) 940-4867
The relationship between depression and the menstrual cycle is complex and may affect different people in different ways. And while both depression and its treatments can affect your monthly cycle, there are also ways to mitigate these effects.
The effects of both depression and menstruation have a significant bearing on your daily life, so it's natural to have questions. You might wonder, can depression delay my period? Will antidepressants affect my menstrual cycle? To answer these and more, here's a look at the evidence.
Firstly, how does a
"normal" menstrual cycle work? Roughly once a month (every
24 to 38 days), the ovaries release an egg, and the uterus thickens its lining (endometrium) in preparation for pregnancy. If the egg is not fertilized, the endometrium sheds as a period—a mixture of blood, mucus, and tissue. Remember: your cycle is more than just your period, and everyone's experience may differ.
Yes, it can. There is research that shows that people with anxiety typically have shorter periods, and people with depression are more likely to have irregular cycles. One of the most common causes of delayed or missed periods is functional hypothalamic amenorrhea, or stress-induced anovulation. This is essentially a survival mechanism: your body decides it isn't a good time to be worrying about reproduction and presses pause on ovulation. Not ovulating disrupts the cycle; your periods may stop, or they may become more irregular. This can be triggered simply by the emotional stress of depression or by changes to your appetite and diet if you undereat when you feel depressed.
Besides the link between depression and the menstrual cycle, there's also evidence that antidepressant medication can affect your periods. For some people, this may mean an increase in symptoms, such as painful, heavy, or irregular periods. Research found that women who were taking antidepressants had "significantly higher" rates of menstrual disorders than those who weren't. Researchers concluded that these symptoms "appear to be associated with antidepressant use at least in some women."
Antidepressants affect the chemical serotonin, a neurotransmitter associated with depression and anxiety. However, serotonin also
plays a role in blood clotting. This could explain why antidepressants seem to increase the risk of heavy bleeding. Some antidepressants have also been linked to
high levels of the hormone prolactin, which can prevent ovulation. This may result in disruption to your cycle, such as missing or irregular periods or changes to your menstrual flow.
It's also worth noting that the connection between depression and the menstrual cycle works both ways. A study published in 2005 found that 64 percent of women with depression experience "premenstrual exacerbation." In other words, the depression symptoms get worse for most women during the five to 10 days before their periods. For women with premenstrual dysphoric disorder, premenstrual symptoms of depression can be particularly severe and may even lead to suicidal thoughts.
If depression or antidepressants are disrupting your menstrual cycle, talk with your doctor. There's no one-size-fits-all solution, but lifestyle changes may help you lessen the stress-induced effects. As much as possible, try to make sure that you're eating enough to fuel your body, sleeping enough to rest, and exercising moderately. Gentle movement, such as walking and yoga, can help ease stress, as can breathing or mindfulness exercises and journaling.
If antidepressant medication seems to make your symptoms worse, speak to your doctor about non-pharmaceutical treatments for depression. These could include talking therapies, such as counseling or cognitive behavioral therapy, or transcranial magnetic stimulation therapy.
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NeuroStar Adult Indications for Use
The NeuroStar Advanced Therapy System is indicated for the treatment of depressive episodes and for decreasing anxiety symptoms for those who may exhibit comorbid anxiety symptoms in adult patients suffering from Major Depressive Disorder (MDD) and who failed to achieve satisfactory improvement from previous antidepressant medication treatment in the current episode.
The NeuroStar Advanced Therapy System is intended to be used as an adjunct for the treatment of adult patients suffering from Obsessive-Compulsive Disorder (OCD).
NeuroStar Adolescent Indications for Use
NeuroStar Advanced Therapy is indicated as an adjunct for the treatment of Major Depressive Disorder (MDD) in adolescent patients (15-21).
Important Safety Information
NeuroStar Advanced Therapy is only available by prescription. A doctor can help decide if NeuroStar Advanced Therapy is right for you. Patients’ results may vary.
The most common side effect is pain or discomfort at or near the treatment site. These events are transient; they occur during the TMS treatment course and do not occur for most patients after the first week of treatment. There is a rare risk of seizure associated with the use of TMS therapy (<0.1% per patient).
Visit neurostar.com for full safety and prescribing information.
Important Safety Information
What is the most important information I should know about SPRAVATO®?
SPRAVATO® can cause serious side effects, including:
Do not take SPRAVATO® if you:
If you are not sure if you have any of the above conditions, talk to your healthcare provider before taking SPRAVATO®.
Before you take SPRAVATO®, tell your healthcare provider about all of your medical conditions, including if you:
Tell your healthcare provider about all the medicines that you take, including prescription and over-the-counter medicines, vitamins and herbal supplements. Taking SPRAVATO® with certain medicine may cause side effects.
Especially tell your healthcare provider if you take central nervous system (CNS) depressants, psychostimulants, or monoamine oxidase inhibitors (MAOIs) medicine. Keep a list of them to show to your healthcare provider and pharmacist when you get a new medicine.
How will I take SPRAVATO®?
What should I avoid while taking SPRAVATO®?
Do not drive, operate machinery, or do anything where you need to be completely alert after taking SPRAVATO®. Do not take part in these activities until the next day following a restful sleep. See “What is the most important information I should know about SPRAVATO®?”
What are the possible side effects of SPRAVATO®?
SPRAVATO® may cause serious side effects including:
See “What is the most important information I should know about SPRAVATO®?”
Increased blood pressure. SPRAVATO® can cause a temporary increase in your blood pressure that may last for about 4 hours after taking a dose. Your healthcare provider will check your blood pressure before taking SPRAVATO® and for at least 2 hours after you take SPRAVATO®. Tell your healthcare provider right away if you get chest pain, shortness of breath, sudden severe headache, change in vision, or seizures after taking SPRAVATO®.
Problems with thinking clearly. Tell your healthcare provider if you have problems thinking or remembering.
Bladder problems. Tell your healthcare provider if you develop trouble urinating, such as a frequent or urgent need to urinate, pain when urinating, or urinating frequently at night.
The most common side effects of SPRAVATO® include:
If these common side effects occur, they usually happen right after taking SPRAVATO® and go away the same day.
These are not all the possible side effects of SPRAVATO®.
Call your doctor for medical advice about side effects. You may report side effects to Johnson & Johnson at 1-800-526-7736, or to the FDA at 1-800-FDA-1088.
What is SPRAVATO® (esketamine) CIII nasal spray?
SPRAVATO® is a prescription medicine used:
SPRAVATO® is not for use as a medicine to prevent or relieve pain (anesthetic). It is not known if SPRAVATO® is safe or effective as an anesthetic medicine.
It is not known if SPRAVATO® is safe and effective for use in preventing suicide or in reducing suicidal thoughts or actions. SPRAVATO® is not for use in place of hospitalization if your healthcare provider determines that hospitalization is needed, even if improvement is experienced after the first dose of SPRAVATO®.
It is not known if SPRAVATO® is safe and effective in children.
Please see full Prescribing Information, including Boxed WARNINGS, and Medication Guide for SPRAVATO® and discuss any questions you may have with your healthcare provider.
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