Azel 160mg Tablet

Azel 160mg tablet is a prescription based medicine as determined by the doctor. The medicine is used in the treatment of advanced prostate cancer in adult men. It works by blocking the male hormones called testosterone which is responsible for the growth of cancer cells in the body. Its active ingredient is Enzalutamide which belongs to the class of androgen receptor inhibitor. It prevents the stimulation of prostate cancer cell growth and induces apoptosis in malignant cells. Doctor recommend this medicine first line therapy for patients metastatic castration prostate cancer (mCRPC) and where the cancer continuous to progress despite androgen deprivation therapy.

Prostate cancer

Like other medication Azel 160mg tablet may cause certain side effects some patients may experience mild effects that resolve on their own while others may require proper medical attention to manage and recover from the symptoms. Discuss with the doctor whether the symptoms worsened or caused significant discomfort:
● Fatigue and weakness
● Hot flushes
● Muscle pain
● Joint discomfort
● Headaches
● Dry skin
● Diarrhea
● Nausea
● High blood pressure
● Memory difficulties
● Upper respiratory tract infections

Azel 160mg should be taken with or without food, preferably at the same time everyday. Taking it in the wrong way may cause severe side effects. It may take several weeks or months to show the most benefit but consistency is key. The doctor will decide what dose is necessary and how often you need to take it. Do not miss the dose and double up on the missed one without consultation to a healthcare professional.

Prostate gland is a part of the male reproductive system, located below the bladder. Its main work is to produce seminal fluid with the help of testosterone hormone. Azel 160mg tablet blocks testosterone which is the main source of cancer cell formation in the body. The medicine stops the growth of tumor cells and prevents from multiplication of cancer cells.

• Tel, G. W., & Tel, G. W. C. antagonist. Although GW9662 itself did not affect AT1R expression, preincubation with GW9662 blocked AT1 R suppression induced by Tel (Fig. 5).
• Antiallergic, A. (1999). C15H19Cl2N3O4 Glaxo Wellcome. Drugs of the Future, 24(7), 789-830.
• Gawas, P. P., Ramakrishna, B., Veeraiah, N., & Nutalapati, V. (2021). Multifunctional hydantoins: Recent advances in optoelectronics and medicinal drugs from Academia to the chemical industry. Journal of Materials Chemistry C, 9(46), 16341-16377.
• Xu, H., Huang, X., Risérus, U., Cederholm, T., Lindholm, B., Ärnlöv, J., & Carrero, J. J. SP030 URINARY ALBUMIN EXCRETION, BLOOD PRESSURE CHANGES AND HYPERTENSION INCIDENCE IN THE COMMUNITY: EFFECT MODIFICATION BY KIDNEY FUNCTION.
• Patisaul, H. B. (2001). Neuroendocrine effects of dietary phytoestrogens. Emory University.