Evaluation of efficacy and safety profile of tamsulosin in benign prostatic hyperplasia


  • Praveen R. Department of Pharmacology, Venkateshwara Institute of Medical Sciences, Gajraula, Uttar Pradesh, India
  • Kumar T. N. Department of Pharmacology, Sree Narayana Institute of Medical Sciences, Ernakulam, Kerala, India




Benign prostatic hyperplasia, Tamsulosin, Post void residual urine


Background: To evaluate the efficacy and safety profile of alpha-1A receptor subtype specific antagonist-tamsulosin in benign prostatic hyperplasia.

Methods: An open label, non-randomised, prospective, single centred study who were visiting urology department with confirmed diagnosis of benign prostatic hyperplasia (BPH) were included in the study. Thirty patients with BPH were prescribed tamsulosin and were followed up to three months. The initial or baseline data collected were identification of the patients such as international prostate symptom score (IPSS), prostate specific antigen, urine analysis, and ultrasonography of prostate including post void residual urine. The patients were followed up to 3 months to measure clinical and laboratory outcomes (IPSS score, post void residual urine, uroflow rates etc.).

Results: In our study, patients receiving tamsulosin 0.4 mg once daily showed a significant improvement in post-void residual urine (PVRU), uroflow rates and IPSS score. The improvements in the above parameters were found to be statistically insignificant at first and third month of follow-up.

Conclusions: In our study, tamsulosin an alpha-1A receptor subtype specific antagonist showed significant improvement in BPH symptoms and the drug was well tolerated.


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How to Cite

R., P., & T. N., K. (2020). Evaluation of efficacy and safety profile of tamsulosin in benign prostatic hyperplasia. International Journal of Basic & Clinical Pharmacology, 9(2), 332–335. https://doi.org/10.18203/2319-2003.ijbcp20200186



Original Research Articles