Vyleesi (bremelanotide) is an agonist of melanocortin receptor given to treat premenopausal women experiencing acquired, generalized hypoactive sexual desire disorder (HSDD) as marked by low sexual desire that produces agony or interpersonal struggle which is not because of a co-existing physical or emotional condition, difficulties among the relationship, or the influences of a medicine or drug material.
Recommended Dosage The suggested dosage of VYLEESI for administration is 1.75 mg injected subcutaneously in the thigh or abdomen, at least 30-45 mins before predicted sexual activity. The span of effectiveness after every dose is untold and the optimal range for Vyleesi intake has yet not been standardized. Patients might choose the time for its administration depending on how they encounter the continuation of impact on sexual desire or any unfavorable reactions like nausea. Indications VYLEESI is prescribed for the treatment of acquired hypoactive sexual desire disorder (HSDD) in women before they have entered menopause. Acquired HSDD concerns HSDD that occurs in a sufferer who earlier experienced no challenges with sexual desire. Generalized HSDD is the type of HSDD that happens without any reason linked with situation, stimulation, or partner. Side effects Bremelanotide might darken the shade of your gums or skin (particularly the skin of the face and breasts). Individuals having darker skin tone might be more prone to acquire this adverse effect. These changes in the skin might remain permanently, even following the discontinuation of bremelanotide administration. Communicate with your physician regarding your risk. General side effects may comprise:
Get prompt medical assistance if you develop symptoms of allergy, such as hives, troublesome breathing, inflammation of your face, lips, throat, or tongue. Contact your specialist instantly if you encounter:
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January 2024
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