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Tamsulosin – ARISTO Pharma – 0.4 mg prolonged-release tablets – Urologikum. Tamsulosin, sold under the brand names including Flomax and Contiflo, is a medication used to treat symptomatic benign prostatic hyperplasia (BPH) and chronic prostatitis and to help with the passage of kidney stones.
Retrograde ejaculation is a common side effect of medications, such as tamsulosin, [6] that are used to relax the muscles of the urinary tract, treating conditions such as benign prostatic hyperplasia. By relaxing the bladder sphincter muscle, the likelihood of retrograde ejaculation is increased.
It is a combination of two previously existing medications: dutasteride, brand name Avodart, and tamsulosin, brand name Flomax. It contains 0.5 mg of dutasteride and 0.4 mg of tamsulosin hydrochloride. [2] Jalyn was the result of the CombAT (Combination of Avodart and Tamsulosin) trial of 2008.
Try a Lower Dose of Your Medication. Clinical trials of Viagra, Cialis and other treatments for ED show that headaches tend to become more common as the prescribed dosage increases.
However, the decrease in depressive symptoms from antidepressants make it worth the sexual side effects for many people. They can be managed by changing the dose, switching drugs, or taking "antidotes". [37] Maca, a plant that grows in central Peru, aids with sexual dysfunction caused by antidepressant drugs for women. There are specific Maca ...
Why might these drugs be linked to longevity? It’s important to point out that this study only found a link between these medications and longevity. Meaning, it didn’t prove that taking any of ...
Female arousal often requires both emotional and physical foreplay, and that takes time, Laino says. Practical issues can also lead to the longer time to orgasm for women, O'Reilly says.
For the same reason, women who are currently pregnant should never take dutasteride. [25] People taking dutasteride should not donate blood to prevent birth defects if a pregnant woman receives blood and should also not donate blood for at least 6 months after the cessation of treatment due to the drug's long elimination half-life .