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Rogaine Side Effects – Telogen Effluvium and Pericardial Effluvium After Discontinuance of Rogaine

If you have recently discontinued the use of Rogaine, it may be a good idea to take note of some potential side effects. These include Telogen effluvium and Pericardial effusions. While not serious, these side effects can occur if you don’t stop using Rogaine immediately.

Rogaine shedding from minoxidil

When you are discontinued use of rogaine, you can expect to experience some shedding for a few months. However, shedding should not be viewed as a negative side effect. Instead, think of it as a sign that you are making progress in treating your alopecia. The main reason for this is that minoxidil has an effect on the hair follicles. If the follicles were not affected by minoxidil, shedding would not occur. As a result, the new hair shafts would remain in anagen longer and grow longer. The final results are typically noticed about twelve months into treatment, but shedding is normal during this time.

Shedding is a normal part of the Rogaine treatment and is a good sign that the medication is working. The hair follicles need to shed their old hair in order to move from a resting phase to an active growth phase. When Rogaine is used for a prolonged period, the medication increases blood flow to the follicles. This increased blood volume carries more nutrients and oxygen. However, when you stop using Rogaine, your hair follicles lose blood supply, which causes them to shrink. As a result, your hair growth will slow down.

Telogen effluvium

A patient who experiences shedding after discontinuation of a hair loss treatment, such as Rogaine, may have a condition known as telogen effluvium. This condition results from the premature shedding of resting hair, which is often called club hair. Telogen hair is a different kind of hair than anagen hair, which has a pointed or tapered tip. In some cases, telogen effluvium can persist for years. It often affects women with thick, long hair, and can mask a condition like genetic baldness.

Affected people may experience a hair loss treatment that works for their unique condition. However, this is not a quick fix. A patient must be consistent with the application of minoxidil over several months before they will notice any noticeable results. Usually, it takes three months to see any significant change in the amount of hair growth caused by minoxidil.

Minoxidil acts as a vasodilator, which means that it widens blood vessels and enhances blood flow to the scalp. The increased blood flow boosts nutrients and oxygen to the hair follicles. The increased blood flow will help shift the hair follicles from the telogen phase to the anagen phase, resulting in more thick hair growth.

Pericardial effusions

Pericardial effusions after discontinuance of rogaine shedding from minoxidil can occur in a variety of clinical situations. In patients with pre-existing heart failure or renal failure, pericardial effusion may be a complication. In severe cases, pericardiocentesis may be necessary.

Minoxidil should not be used by women who are pregnant or breastfeeding. Although the American Academy of Pediatrics considers minoxidil to be compatible with breastfeeding, some other experts are less confident in its safety. In addition, minoxidil is quickly excreted from the body into breast milk. The adverse effects of minoxidil during breastfeeding have not been documented in infants older than 2 months.

Minoxidil is approved for the treatment of androgenetic alopecia. Although it is rare to develop a major systemic toxicity following topical application, it is important to note that central serous chorioretinopathy can occur. This condition can affect the retina or other parts of the body. In a recent case, a 37-year-old man complained of subjective and objective changes of his vision, including impaired dark adaptation and positive relative scotoma. He denied taking any other drugs. His dilated fundus revealed a central swelling of the macula and subretinal fluid. Optical coherence tomography revealed subretinal fluid, and fluorescein angiography revealed a focal hyperfluorescent spot.

Propylene glycol in minoxidil

Propylene glycol is a common ingredient in many over-the-counter topical hair loss treatments. It acts as an emulsifier and solvent. It is also an irritant and can cause allergic reactions. It can also cause dry hair. Therefore, many people who use Minoxidil as a treatment for hair loss choose not to use it.

One of the side effects of minoxidil is contact dermatitis. Many of the side effects associated with Rogaine are caused by its propylene glycol content. For this reason, it is important to use a product that doesn’t contain propylene glycol. Unlike the topical versions, foam minoxidil contains no propylene glycol, making it a good alternative for Rogaine users who are experiencing contact dermatitis. Furthermore, despite its reputation as a topical hair loss treatment, minoxidil has the potential to have systemic side effects when you overdose on it. In rare cases, minoxidil can enter the bloodstream and cause anaphylactic shock.

Conclusion

Propylene glycol is also known to cause allergic reactions. One study performed at the University of Oregon Department of Dermatology showed that 12 out of 84 people tested developed skin reactions to the ingredient. However, these reactions are not common. Propylene glycol is commonly used in cosmetic products, such as shampoos and deodorants. Although it has been associated with some risks, it is generally recognized as safe by the FDA.

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