Dapox 30mg Tablet: Uses, Benefits and Side Effects

Natural variable PE is regarded as a normal variant of sexual performance, whereas premature-like ejaculatory dysfunction is defined as a complaint of PE superimposed on ejaculation time in the normal range (10). These new subtypes help physicians more precisely stratify patients and set treatment algorithms. Pharmacotherapy remains the basis of management of lifelong and acquired PE, whereas psychotherapy should be considered for patients with natural variable PE and premature like ejaculatory dysfunction (12).

Can I Take Tadalafil With Dapoxetine?

In the evolving landscape of pharmaceuticals, the Dapox 30mg tablet stands out as a significant breakthrough for individuals with specific health conditions. This article delves into the tablet’s myriad benefits, uses, side effects, and how it improves patients’ quality of life. ED drugs don’t work directly on ejaculation times — but they go a long way towards boosting confidence during sex, which may alleviate the most common cause of PE — sexual performance anxiety.

It’s reasonable to expect some change to occur simply by entering the study — as seen in the placebo control group. This concept is called the Pygmalion effect — which is a psychological phenomenon where having expectations that something will work leads to improvement. Other antidepressants can also interact with dapoxetine because of the shared pathways these drugs have on the body. The larger 60 mg dose is much more likely to cause side effects, so doctors usually start with the smaller dose, and only increase to the 60 mg option if the 30 mg pill doesn’t work.

• It is unclear whether tadalafil, the active ingredient in Cialis, passes into breast milk or if it could have any adverse effects on the nursing infant.
• Microstimulation of the medullary reticular formation decreases the amplitude and increases the latency of PMRD (90).
• They can provide personalized advicе based on your specific situation and guide you towards the mоst suitable trеatment choices.
• In Korea and other areas of the Far East, SS (Super Secret) cream (a combination of 9 ingredients, mainly herbal) has been shown to desensitize the penis, decrease the vibratory threshold, and help men with premature ejaculation to delay their ejaculatory response significantly.
• Before dapoxetine was approved for the treatment of lifelong premature ejaculation (LPE) in China, daily dosing with off-label sertraline was common.

At all doses, dapoxetine significantly reduced the proportion of rats displaying PCA-induced ejaculation in a dose-dependent manner, from 78% of rats with vehicle to 33%, 22% and 13% of rats following intravenous dapoxetine 1, 3 and 10 mg/kg, respectively. Dapoxetine significantly decreased the AUC of PCA-induced intraseminal vesicle pressure increases and bulbospongiosus muscle contractile bursts by 78% at all doses, by 91% following dapoxetine 1 and 10 mg/kg, and by 85% following dapoxetine 3 mg/kg. Articles involving dapoxetine for the treatment of PE were identified, with priority given to systematic reviews, meta-analyses and integrated analyses, double-blind, randomized, placebo-controlled clinical trials (RCTs), and nonrandomized observational studies. The references listed in identified articles were used as a further source of relevant studies. While it’s not clear exactly how modafinil works for this condition, studies have shown the drug can improve ejaculation latency time in Lifelong premature ejaculation 6 — which is a notoriously difficult form of PE to treat. During phase III clinical testing, detailed documentation of each side effect was recorded for the 30 and 60 mg doses.

Phase III trials

This prospective study included LPE patients who previously attempted treatment with sertraline and who agree to receive dapoxetine therapy in our hospital from January 2020 to March 2021. Patients who received any PE therapy in the two months prior to the dapoxetine therapy were excluded. All patients received dapoxetine 30 mg (taken 1–3 hours before sexual intercourse) for 12 weeks, and they were not taking sertraline during the trial.

Despite several promising clinical trials, the drug remains unavailable in the United States. In this study, we used CGIC to evaluate the satisfaction of dapoxetine and sertraline for the treatment of LPE. CGIC is a self-evaluation assay based on patients’ subjective feelings; so, it is not as objective a measure as IELT and may be influenced by physical or psychological factors. However, somehow, PE itself is a kind of subjective concept based on the PE diagnostic criteria14, and we should understand that patients’ satisfaction is our primary treatment target, especially among patients with PE.

It’s important to consult with a healthcare professional to determine which medication is most suitable based on individual circumstances and medical histоry. The first step is to attempt to relieve any underlying performance pressure on the male. If premature ejaculation occurs when intercourse is attempted, the couple should be instructed not to attempt intercourse until the ejaculatory problem is treated. In the meantime, the male may use manual stimulation, oral sex, or other means to satisfy the female partner. Regardless of the mechanism, PDE5 inhibitors have been found to be safe and effective as a therapeutic adjunct for premature ejaculation in men for whom such therapy is not otherwise contraindicated.

However, treatment of lifelong PE with PDE5-inhibitors in such situations is not recommended (level of evidence 4) and further evidence-based research is encouraged to understand these conflicting data (14). In a second pharmacokinetic study, single doses and multiple doses of dapoxetine (30 mg, 60 mg) were evaluated in a randomized, open-label, two-treatment, two-period, crossover study of 42 healthy male volunteers over 9 days Modi et al. 2006. Subjects received a single dose of dapoxetine 30 mg or 60 mg on day 1 (single-dose phase) and on days 4–9 (multiple-dose phase). Dapoxetine was rapidly absorbed, with mean maximal plasma concentrations of 297 and 498 ng/ml at 1.01 and 1.27 h after single doses of dapoxetine 30 and 60 mg, respectively (Table 1). Elimination of dapoxetine was rapid and biphasic, with an initial half life of 1.31 and 1.42 h, and a terminal half life of 18.7 and 21.9 h following single doses of dapoxetine 30 and 60 mg, respectively. The pharmacokinetics of dapoxetine and its metabolites were not affected by repeated daily dosing and steady state plasma concentrations were reached within 4 days, with only modest accumulation of dapoxetine (approximately 1.5 fold) (Figure 2(b)).

Multiple well controlled evidence-based studies have demonstrated the efficacy and safety of SSRIs in delaying ejaculation, confirming their role as first-line agents for the treatment of lifelong and acquired PE Waldinger et al. 2004. A total of 144 patients with LPE completed this study; including 64 patients who reported that previous sertraline treatment was satisfactory (group A) and 80 patients for whom previous sertraline therapy was unsatisfactory in treating PE (group B). Both groups experienced significantly increased intravaginal ejaculatory latency time. Dapoxetine therapy was reported satisfactory by 67.5% of patients with LPE in whom sertraline therapy unsatisfactory according to their Clinical Global Impression of Change score, which was not different from those who reported this result in group A (62.5%). Similar outcomes were also reported for premature ejaculation profile and steroids in USA treatment-emergent adverse events. Even in more extreme cases of PE, in which baseline IELT was very short, treatment with dapoxetine effectively increased IELT.