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Journal articles on the topic 'Dapoxetine'

Author: Grafiati

Published: 3 June 2025

Last updated: 1 August 2025

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1

&NA;. "Dapoxetine." Drugs in R & D 6, no. 5 (2005): 307–11. http://dx.doi.org/10.2165/00126839-200506050-00007.

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Hoy, Sheridan M., and Lesley J. Scott. "Dapoxetine." Drugs 70, no. 11 (2010): 1433–43. http://dx.doi.org/10.2165/11204750-000000000-00000.

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Bidakia, Akram Zare, Mohsen Zabihib, Mohadeseh Asadic, and Reza Bidakid. "The effect of Dapoxetine on Chronic Constriction Injury (CCI) induced neuralgia in rats." Romanian Journal of Neurology 21, no. 1 (2022): 34–39. http://dx.doi.org/10.37897/rjn.2022.1.6.

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Introduction. Recent studies have shown that SSRIs have anti-inflammatory effects, and their administration prevents their production by acting on inflammatory cytokines. Emphasizing that we did not find a study on Dapoxetine and its effect on neuropathic pain, in this study, we examined the effect of Dapoxetine on neuropathic pain in rats. Material and methods. 42 rats were divided into six groups of 7, which included: sham, control, gabapentin, Duloxetine and Dapoxetine 1 and 3. Except for the sham group, other groups were induced with neuropathy, and no drug treatment was performed in the s

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Zhang, Xin, Zhanwang Gao, Fei Qin, Kehan Chen, Jiansong Wang, and Lingli Wang. "Determination of Dapoxetine Hydrochloride in Human Plasma by HPLC–MS/MS and Its Application in a Bioequivalence Study." Molecules 27, no. 9 (2022): 2707. http://dx.doi.org/10.3390/molecules27092707.

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Dapoxetine is used for the treatment of premature ejaculation. The present study developed an HPLC–MS/MS method to determine the levels of dapoxetine in human plasma processed using simple protein precipitation. Dapoxetine-d7 was selected as the internal standard. The established method was performed using a mass spectrometer equipped with an electrospray ionization source in multiple positive ion reactions to monitor the mode using the precursor-to-product ion transitions of m/z 306.2–157.2 and m/z 313.2–164.2 for dapoxetine-d7 and dapoxetine, respectively. The method was evaluated based on i

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McMahon, Chris G. "Efficacy of Dapoxetine in the Treatment of Premature Ejaculation." Clinical Medicine Insights: Reproductive Health 5 (January 2011): CMRH.S7337. http://dx.doi.org/10.4137/cmrh.s7337.

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Introduction Premature ejaculation (PE) is a common male sexual disorder which is associated with substantial personal and interpersonal negative psychological factors. Pharmacotherapy of PE with off-label antidepressant SSRI drugs is common. Development and regulatory approval of drugs specifically for the treatment of PE will reduce reliance on off-label treatments and serve to fill a unmet treatment need. Aimml To review evidence supporting the efficacy and safety of dapoxetine in the treatment of PE. Methods MEDLINE and the proceedings of major international and regional scientific meeting

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Santosh A. Waghmare, Pranit B. Kale, and Arun M. Kashid S. B. Wankhede. "Bioanalytical Method Development and Validation of Dapoxetine Hydrochloride in Human Plasma by RP-HPLC." International Journal of Current Microbiology and Applied Sciences 10, no. 10 (2021): 21–35. http://dx.doi.org/10.20546/ijcmas.2021.1010.004.

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A simple, accurate and rapid Bioanalytical reverse phase high performance liquid chromatography (RPHPLC) method for determination of Dapoxetin hydrochloride in human plasma was validated as per ICH guideline. Dapoxetin hydrochloride is significantly superior in premature ejaculation and more active against serotonin transport inhibitor than any other drug in class. The total analysis was carried out on using stationary phase symmetry C1 (4.6mm X 250mm, 5µm) with Mobile Phase Acetonitrile: Buffer (60:40) pH adjusted to3.5 flow rate was 1.0 ml/min, injection volume of 10 ppm and detection wavele

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7

Sorbera, L. A., J. Castañer, and R. M. Castañer. "Dapoxetine Hydrochloride." Drugs of the Future 29, no. 12 (2004): 1201. http://dx.doi.org/10.1358/dof.2004.029.12.865936.

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Gadiya, Hemesh, Monika Maheshwari, and Ashok Dashora. "UV-ANALYTICAL METHOD DEVELOPMENT AND VALIDATION FOR SIMULTANEOUS ESTIMATION OF DAPOXETINE HYDROCHLORIDE AND SILDENAFIL CITRATE IN TABLET DOSAGE FORM." Asian Journal of Pharmaceutical and Clinical Research 12, no. 1 (2019): 328. http://dx.doi.org/10.22159/ajpcr.2018.v12i1.29937.

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Objective: The objective of this research was to develop and validate a simple ultraviolet (UV) spectrophotometric method for simultaneous determination of sildenafil citrate and dapoxetine hydrochloride in a pharmaceutical formulation.Methods: Two simple UV spectrophotometric methods have been developed for simultaneous determination of sildenafil citrate and dapoxetine hydrochloride. For both methods, stock solutions were prepared in methanol followed by the further required dilutions with methanol. Proposed dual-wavelength method and ratio derivative method, the wavelength of maximum absorp

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Gadiya, Hemesh, Monika Maheshwari, and Ashok Dashora. "UV-ANALYTICAL METHOD DEVELOPMENT AND VALIDATION FOR SIMULTANEOUS ESTIMATION OF DAPOXETINE HYDROCHLORIDE AND SILDENAFIL CITRATE IN TABLET DOSAGE FORM." Asian Journal of Pharmaceutical and Clinical Research 12, no. 1 (2019): 328. http://dx.doi.org/10.22159/ajpcr.2019.v12i1.29937.

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Objective: The objective of this research was to develop and validate a simple ultraviolet (UV) spectrophotometric method for simultaneous determination of sildenafil citrate and dapoxetine hydrochloride in a pharmaceutical formulation.Methods: Two simple UV spectrophotometric methods have been developed for simultaneous determination of sildenafil citrate and dapoxetine hydrochloride. For both methods, stock solutions were prepared in methanol followed by the further required dilutions with methanol. Proposed dual-wavelength method and ratio derivative method, the wavelength of maximum absorp

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10

Khan, Sarhad, Khalid Farooq, and Najma Hameed. "COMPARISON OF PAROXETINE AND DAPOXETINE IN PREMATURE EJACULATION." Khyber Journal Of Medical Sciences 15, no. 3 (2022): 112–17. https://doi.org/10.70520/kjms.v15i3.203.

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Objective: To compare the efficacy of Paroxetine and Dapoxetine in premature ejaculation.Methodology: We enrolled One hundred and twenty-six patients in this study from January 2019to December 2021 in urology department Medical teaching institute Lady Reading hospitalPeshawar by using convenient sampling technique. Patients were assigned to take either 20mgOD Paroxetine (n =158) or 30mg OD Dapoxetine(n=159). On follow-up after six weeks, all thepatients were assessed for improvement in intravaginal ejaculation latency timings (IELT). T testwas applied to see any significant difference in both

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11

Zhao, Guo-Jiang, Qiang Guo, Yu-Feng Li, and Yan-Gang Zhang. "Efficacy and safety of dapoxetine for premature ejaculation: an updated systematic review and meta-analysis." Sexual Health 16, no. 4 (2019): 301. http://dx.doi.org/10.1071/sh18005.

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We conducted a systematic review and meta-analysis of published randomised controlled trials of dapoxetine for premature ejaculation. We systematically searched Embase, PubMed, Cochrane, Web of Knowledge, FDA.gov and Clinical Trials.gov for studies reporting dapoxetine in men with premature ejaculation. Efficacy endpoints included intravaginal ejaculatory latency times (IELT), personal distress related to ejaculation (PDRE) and treatment-emergent adverse events (TEAEs) was used to evaluate safety. Data were analysed using a random-effects model. Electronic search identified 276 papers. The fin

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12

Wyllie, Michael G. "THE DAPOXETINE PARADOX." BJU International 105, no. 8 (2010): 1041–42. http://dx.doi.org/10.1111/j.1464-410x.2010.09250.x.

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Zhang, Bingzhi, Jianchen Yu, Ge Zhu, et al. "Dapoxetine, a Selective Serotonin Reuptake Inhibitor, Suppresses Zika Virus Infection In Vitro." Molecules 28, no. 24 (2023): 8142. http://dx.doi.org/10.3390/molecules28248142.

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Zika virus (ZIKV) belongs to the Flavivirus genus of the Flaviviridae family, and is a pathogen posing a significant threat to human health. Currently, there is a lack of internationally approved antiviral drugs for the treatment of ZIKV infection, and symptomatic management remains the primary clinical approach. Consequently, the exploration of safe and effective anti-ZIKV drugs has emerged as a paramount imperative in ZIKV control efforts. In this study, we performed a screening of a compound library consisting of 1789 FDA-approved drugs to identify potential agents with anti-ZIKV activity.

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14

Pavone, Carlo, Cristina Scalici Gesolfo, Daniela Abbadessa, et al. "Compliance to Therapy with Dapoxetine in Patients Affected by Premature Ejaculation." Urologia Journal 80, no. 1 (2013): 56–63. http://dx.doi.org/10.5301/ru.2013.10763.

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Introduction Premature ejaculation (PE) is a sexual dysfunction with high prevalence. According to some reports, it is present in about 20-30% of the male population. Since 2009 PE has been treated with a novel inhibitor of serotonin re-uptake, Dapoxetine, which has been reported to be specifically active for PE. Materials and Methods 59 patients have been selected among the patients affected by PE observed at the outpatient department of Urology and Andrology of the “Paolo Giaccone” University Policlinic Hospital of Palermo. Diagnosis was confirmed unequivocally in all patients, who were suit

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Akhavan Rezayat, Alireza, Amirabbas Asadpour, Samaneh Boroumand-Noughabi, Mona Kabiri, Elham Ghafarian Baghaei Moghadam, and Alireza Nough Javazm. "Investigation of the effects of oral dapoxetine on kidney function and histopathologic changes in male rats; an animal study and future perspectives." Journal of Nephropharmacology 13, no. 1 (2023): e10633. http://dx.doi.org/10.34172/npj.2023.10633.

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Introduction: Dapoxetine is a novel therapeutic agent employed in treating specific diseases. However, its potential impact on renal excretion processes has yet to be thoroughly investigated, necessitating further exploration in this study. Objectives: This research aimed to assess the effects of dapoxetine on renal function and explore any potential disturbances in kidney excretion processes. Materials and Methods: In this study, 32 male Albino rats weighing between 200-250 g were utilized. The rats were randomly divided into four groups. Group one served as the control and received a normal

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Sikdar, Tushar Kanti, Moushumi Chowdhury, Mohammad Shamsul Ahsan, and Rubaiya Ali. "Dapoxetine for the management of premature ejaculation." Bangladesh Journal of Psychiatry 31, no. 1 (2020): 15–19. http://dx.doi.org/10.3329/bjpsy.v31i1.45367.

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Premature ejaculation is the most prevalent male sexual disorder and is more common in South Asia. Bangladesh is no exception. Premature ejaculation causes dissatisfaction in the relationship, frustration for the patient and partner as well as reason of marital failure. Since 1970s sex therapy was the mode of treatment for premature ejaculation. Now treatment with drugs also seems effective. Now a days dapoxetine is used in Bangladesh for the treatment of premature ejaculation. The aim of the study was to determine the efficacy and tolerability of dapoxetine in patients with premature ejaculat

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17

Skibiński, Robert, Jakub Trawiński, and Maciej Gawlik. "Characterization of Phase I Hepatic Metabolites of Anti-Premature Ejaculation Drug Dapoxetine by UHPLC-ESI-Q-TOF." Molecules 26, no. 13 (2021): 3794. http://dx.doi.org/10.3390/molecules26133794.

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Determination of the metabolism pathway of xenobiotics undergoing the hepatic pass is a crucial aspect in drug development since the presence of toxic biotransformation products may result in significant side effects during the therapy. In this study, the complete hepatic metabolism pathway of dapoxetine established according to the human liver microsome assay with the use of a high-resolution LC–MS system was described. Eleven biotransformation products of dapoxetine, including eight metabolites not reported in the literature so far, were detected and identified. N-dealkylation, hydroxylation

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18

Feige, A. M., M. R. Pinsky, and W. J. G. Hellstrom. "Dapoxetine for Premature Ejaculation." Clinical Pharmacology & Therapeutics 89, no. 1 (2010): 125–28. http://dx.doi.org/10.1038/clpt.2010.215.

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19

McMahon, Chris G. "Dapoxetine for premature ejaculation." Expert Opinion on Pharmacotherapy 11, no. 10 (2010): 1741–52. http://dx.doi.org/10.1517/14656566.2010.493174.

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Vieiralves, Rodrigo R., and Luciano A. Favorito. "Dapoxetine and premature ejaculation." International braz j urol 49, no. 4 (2023): 511–14. http://dx.doi.org/10.1590/s1677-5538.ibju.2023.9908.

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21

Dilsha, P., Richards M. Paul, D. Suchitra, and B. A. Vishwanath. "Validated RP - HPLC Method for Simultaneous Estimation of Tadalafil and Dapoxetine in Combined Pharmaceutical Dosage Forms." International Journal of Current Science Research and Review 05, no. 09 (2022): 3558–63. https://doi.org/10.5281/zenodo.7086291.

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<strong>ABSTRACT</strong> <strong>Aim:</strong> To develop a new, simple, fast, rapid, accurate, efficient and reproducible RP-HPLC method for the simultaneous estimation of Tadalafil and Dapoxetine. <strong>Background: </strong>Estimation of Tadalafil and Dapoxetine is a combination drug of choice used to treat preamature ejaculation in men. <strong>Objective:</strong> The main objective of the Simultaneous estimation of combined drug is to establish identity, physical characteristics and potency of the drugs and to demonstrate the suitability of the assay method to provide useful data to ens

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22

Albu-Salih, Anis Hasan H. "Comparative study between usage of medicine containing a mixture of Dapoxetine and Tadalafil with the usage of these drugs separately in treatment of rapid ejaculation." Muthanna Medical Journal 8, no. 1 (2021): 31–34. http://dx.doi.org/10.52113/1/2410-4590/2021-31-34.

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A study was conducted on 58 patients aged from 18-63 years old, they suffering from rapid ejaculation and all their Intravaginal ejaculation latency time (IELT) were less than 2 minutes. This study done at Erectile dysfunction unit in Al-Muthana teaching hospital for a period of 1 month (March/2019). The patients were divided into 2 groups: Group 1: Patient received 30 mg of Dapoxetine 1hr before coitus and 10 mg of Tadalafil 30 min before coitus. Group 2: Patient received Dapoxetine 20 mg + Tadalafil 10 mg mixed in one tablet 1 hr before coitus. The result of our study revealed that the IELT

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23

Safarinejad, Mohammad R. "Reply: Dapoxetine in Premature Ejaculation." Neuropsychopharmacology 33, no. 11 (2008): 2786–88. http://dx.doi.org/10.1038/npp.2008.12.

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24

Waldinger, Marcel D., Dave H. Schweitzer, and Berend Olivier. "Dapoxetine treatment of premature ejaculation." Lancet 368, no. 9550 (2006): 1869. http://dx.doi.org/10.1016/s0140-6736(06)69773-0.

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Siddiqui, Shafi A., and Kumar V. Srinivasan. "Enantioselective synthesis of (S)-dapoxetine." Tetrahedron: Asymmetry 18, no. 17 (2007): 2099–103. http://dx.doi.org/10.1016/j.tetasy.2007.07.028.

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26

Pavone, Carlo, Daniela Abbadessa, Giuseppa Gambino, Giovanna Scaduto, and Marco Vella. "Premature ejaculation: Pharmacotherapy vs group psychotherapy alone or in combination." Archivio Italiano di Urologia e Andrologia 89, no. 2 (2017): 114. http://dx.doi.org/10.4081/aiua.2017.2.114.

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Objectives: Premature Ejaculation (PE), the commonest sexual dysfunction in males, is generally treated with local anesthetic and SSRI (Dapoxetine). The aim of our study was investigate Group Psychotherapy as an alternative treatment for PE and compare the efficacy of pharmacological treatment and psychotherapy, either alone or in combination, in terms of response and improved Quality of Life (QoL). From a male outpatient population screened for PE, those who received a diagnosis of PE were proposed for the study, enrolled and divided into 3 groups (A, B and C). Each group was treated with Dap

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Bahavarnia, Farnaz, Fereshteh Kohansal та Mohammad Hasanzadeh. "One-drop chemosensing of dapoxetine hydrochloride using opto-analysis by multi-channel μPAD decorated silver nanoparticles: introducing a paper-based microfluidic portable device/sensor toward naked-eye pharmaceutical analysis by lab-on-paper technology". RSC Advances 14, № 4 (2024): 2610–20. http://dx.doi.org/10.1039/d3ra06752a.

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Dapoxetine (DPX) belongs to the selective serotonin reuptake inhibitor (SSRI) class and functions by blocking the serotonin transporter and increasing serotonin activity, thereby delaying ejaculation.

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Rafi, Hira, and Muhammad Farhan. "Dapoxetine: An Innovative Approach in the Therapeutic Management In Animal Model of Depression." Pakistan Journal of Pharmaceutical Research 2, no. 1 (2016): 15. http://dx.doi.org/10.22200/pjpr.2016115-22.

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Stress is a complicated condition that effects on person’s mental and physical health, and it is the precursor of other psychological disorders mainly depression. Serotonin (5-Hydroxytryptamine; 5-HT) is well known to have hypofunction in unpredictable chronic mild stress whereas, unpredictable chronic mild stress (UCMS) has produced the most steady and continuous results of anhedonia and learned helplessness particularly in rats. The stress-induced depressive like behavior can be reversed by many antidepressants such as SSRIs. Selective serotonin [5-hydroxytryptamine (5-HT)] reuptake inhibito

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Darcsi, András, Zoltán Szakács, Ferenc Zsila, Gergő Tóth, Ákos Rácz, and Szabolcs Béni. "NMR, CD and UV spectroscopic studies reveal uncommon binding modes of dapoxetine to native cyclodextrins." RSC Advances 6, no. 104 (2016): 102315–28. http://dx.doi.org/10.1039/c6ra22431h.

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30

Li, Rui-fang, Jun-min Fu, Xing-zhi Lv, et al. "Effects of Evodiamine on the Pharmacokinetics of Dapoxetine and Its Metabolite Desmethyl Dapoxetine in Rats." Pharmacology 97, no. 1-2 (2015): 43–47. http://dx.doi.org/10.1159/000441568.

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Abou-Omar, Mona N., Abdelaziz M. Annadi, Noha M. El Zahar, et al. "Simultaneous determination of Avanafil and Dapoxetine in human plasma using liquid chromatography/tandem mass spectrometry (LC-MS/MS) based on a protein precipitation technique." RSC Advances 11, no. 47 (2021): 29797–806. http://dx.doi.org/10.1039/d1ra05492a.

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32

Salokangas, Raimo KR. "Dapoxetine for treatment of premature ejaculation." Lancet 368, no. 9548 (2006): 1649. http://dx.doi.org/10.1016/s0140-6736(06)69694-3.

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33

Kim, Sun Joo, Tae Hong Jeon, Im Sook Min, In Su Kim, and Young Hoon Jung. "Asymmetric total synthesis of (S)-dapoxetine." Tetrahedron Letters 53, no. 28 (2012): 3680–82. http://dx.doi.org/10.1016/j.tetlet.2012.05.037.

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van der Does, E. "Behandeling van premature ejaculatie met dapoxetine." Medisch-Farmaceutische Mededelingen 45, no. 1 (2007): 17–18. http://dx.doi.org/10.1007/bf03058918.

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35

Chaplin, Steve, and Penny Mostyn. "Dapoxetine: licensed treatment for premature ejaculation." Prescriber 25, no. 8 (2014): 10–14. http://dx.doi.org/10.1002/psb.1189.

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36

Zhu, Yijun, Zhenren Liu, Hongyan Li, Deyong Ye, and Weicheng Zhou. "A novel and practical asymmetric synthesis of dapoxetine hydrochloride." Beilstein Journal of Organic Chemistry 11 (December 17, 2015): 2641–45. http://dx.doi.org/10.3762/bjoc.11.283.

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A novel and practical asymmetric synthesis of dapoxetine hydrochloride by using the chiral auxiliary (S)-tert-butanesulfinamide was explored. The synthesis was concise, mild, and easy to perform. The overall yield and stereoselectivity were excellent.

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37

Naguib, Ibrahim A., Maimana A. Magdy, Basma H. Anwar, and Nessreen S. Abdelhamid. "A Validated Green HPTLC Method for Quantitative Determination of Dapoxetine Hydrochloride and Tadalafil in Bulk and Pharmaceutical Formulations." Journal of Chromatographic Science 58, no. 4 (2020): 303–8. http://dx.doi.org/10.1093/chromsci/bmz115.

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Abstract Dapoxetine hydrochloride (DAP) and Tadalafil (TAD) were separated and determined quantitatively using a validated green high-performance thin layer chromatographic (HPTLC) method in their binary mixtures either as raw materials or in pharmaceutical formulations. The concentration ranges were 0.1–1.6 and 0.2–2.5 μg/band for dapoxetine and tadalafil, respectively, with accuracies of 98.93% ± 0.62 and 99.26% ± 1.39, respectively. Silica gel HPTLC F254 plates were used to carry out the separation. The mobile phase used was a mixture of ethanol–ethyl acetate (1:9 by volume), which is envir

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Нисанбаев, А. Д., А. А. Нисанбаева, Д. И. Сенгирбаев, А. Ж. Суранчиев, and Г. А. Ипосунова. "MODERN CONCEPT OF CONSERVATIVE TREATMENT OF PREMATURE EJACULATION." Vestnik, no. 3 (December 15, 2021): 372–76. http://dx.doi.org/10.53065/kaznmu.2021.39.48.071.

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В данной статье представлен обзор методов консервативного лечения преждевременная эякуляция. Отмечено низкая обращаемость пациентов с данной интимной проблемой, и малая информированность об успешном лечении вышеуказанной нозологии. Эффективным методом выбора является применение селективных ингибиторов захвата серотонина, а именно дапоксетина, который обладает высоким уровнем доказательности и удобен как препарат по требованию. Учеными выявлено эффективное применение дапоксетина и ингибиторов 5 альфа-редуктазы в лечении преждевременной эякуляции. This article provides an overview of the methods

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Park, H., and N. Park. "Discontinuation of Dapoxetine Treatment in Patients with Premature Ejaculation: A 2-Year Prospective Observational Study." Klinička psihologija 9, no. 1 (2016): 66. http://dx.doi.org/10.21465/2016-kp-op-0043.

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Objective: Although dapoxetine is the only oral agent approved for premature ejaculation (PE) and is very effective, its discontinuation rate is high compared to PDE5 inhibitors for ED treatment. We assessed discontinuation rate of dapoxetine in PE and the reasons for discontinuation. Design and Method: The study enrolled 182 patients (mean age 38.2). The PE type (life-long or acquired), self-estimated intravaginal ejaculation latency time (IELT), IIEF-EF questionnaire, and medical history were checked in all patients. The patients were evaluated 1, 3, 6, 12, and 24 months after initiating the

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40

Anandhan, Ramasamy, Mandapati Bhargava Reddy, and Murugesan Sasikumar. "Development of novel triazole based dendrimer supported spiroborate chiral catalysts for the reduction of (E)-O-benzyl oxime: an enantioselective synthesis of (S)-dapoxetine." New Journal of Chemistry 43, no. 38 (2019): 15052–56. http://dx.doi.org/10.1039/c9nj03217g.

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A reusable dendrimer supported spiroborate catalysts 2 and 3 have been synthesized via a “click” chemistry and demonstrated as catalysts for the reduction of (E)-O-benzyl oxime 13 to synthesis of (S)-dapoxetine 14 with 94% ee and 46% overall yield.

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&NA;. "Dapoxetine a satisfying solution to premature ejaculation." Inpharma Weekly &NA;, no. 1491 (2005): 9. http://dx.doi.org/10.2165/00128413-200514910-00016.

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42

Owen, R. T. "Dapoxetine: A novel treatment for premature ejaculation." Drugs of Today 45, no. 9 (2009): 669. http://dx.doi.org/10.1358/dot.2009.45.9.1388694.

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43

Sasikumar, M., and Milind D. Nikalje. "Simple and Efficient Synthesis of (S)-Dapoxetine." Synthetic Communications 42, no. 20 (2012): 3061–67. http://dx.doi.org/10.1080/00397911.2011.575522.

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44

McMahon, Chris. "Dapoxetine in the Treatment of Premature Ejaculation." Clinical Neuropharmacology 30, no. 5 (2007): 314–15. http://dx.doi.org/10.1097/wnf.0b013e31815766f9.

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45

Pryor, Jon L. "Dapoxetine treatment of premature ejaculation – Author's reply." Lancet 368, no. 9550 (2006): 1869–70. http://dx.doi.org/10.1016/s0140-6736(06)69774-2.

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46

Modi, N., M. Dresser, B. Wang, and S. Gupta. "DAPOXETINE PHARMACOKINETICS AND TOLERABILITY IN HYPERTENSIVE MEN." European Urology Supplements 5, no. 2 (2006): 66. http://dx.doi.org/10.1016/s1569-9056(06)60180-2.

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47

Stone, Louise. "Paternal dapoxetine is detrimental to reproductive outcomes." Nature Reviews Urology 12, no. 11 (2015): 598. http://dx.doi.org/10.1038/nrurol.2015.251.

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Akdeniz, Ekrem, Suleyman Sirri Bilge, Mustafa Suat Bolat, et al. "Effect of a carbohydrate rich diet in vas deferens contractility in rats." Medical Science and Discovery 3, no. 6 (2016): 259–65. https://doi.org/10.36472/msd.v3i6.153.

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Abstract:

Objective: We aimed to investigate the effects of a Carbohydrate-rich diet on vas deferens contractility and histology. Materials and Methods: Twenty mature male rats were subjected into two groups. The control group received regular food and water and the study group received regular food and a carbohydrate-rich liquid diet mixture of 37–40% fructose, 30–36% sucrose and 27–30% glucose instead of water and prepared stock diet was diluted with 50% water. Animals were weighted and sacrificed after six weeks and the vas deferens has been evaluated with in vitro studies. Five rats from both the co

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Harrison-Woolrych, Mira. "Patient Reporting Encouragedduring Monitoringof Dapoxetine in New Zealand." Drug Safety 34, no. 11 (2011): 1115–16. http://dx.doi.org/10.2165/11596010-000000000-00000.

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Krishnakumar, P., T. Sundarrajan, M. K. Kathiravan, and K. Manikandan. "Spectroscopic Estimation of Dapoxetine HCl using Multivariate Analysis." Research Journal of Pharmacy and Technology 13, no. 6 (2020): 2715. http://dx.doi.org/10.5958/0974-360x.2020.00483.7.

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