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Dapoxetin > dapoxetine 5mg


  • The pharmacokinetic studies of dapoxetine
  • Safety and tolerability
  • 6. Top 20 FAQs
  • Limitations of the study
  • Buy Dapoxetine Tablets
  • Elective and emergency surgery
  • Adverse effects

Dapoxetine 5mg for Premature Ejaculation Treatment

We are driven to improve the digital healthcare experience and our team is available to help you throughout the process. Safety Information:All ingredients thoroughly researched and tested for safety.

The pharmacokinetic studies of dapoxetine

These pharmacokinetics are more favorable in that they might minimize drug accumulation in the body, habituation, and side effects. Dapoxetine was initially considered unsuccessful in its intended use as an antidepressant; however, it has since been investigated as a possible aid to an approach to depression treatment focused on stress reduction, based on an animal model of depression. Dapoxetine should not be used in men with moderate to severe hepatic impairment and in those receiving CYP3A4 inhibitors such as ketoconazole, ritonavir, and telithromycin. Dapoxetine also cannot be used in patients with heart failure, permanent pacemaker, or other significant ischemic heart disease. Caution is advised in men receiving thioridazine, monoamine oxidase inhibitors, SSRIs, serotonin-norepinephrine reuptake inhibitors, or tricyclic antidepressants.

Differential scanning calorimetry (DSC)

If a patient stops taking one of these drugs, he should wait for 14 days before taking dapoxetine. If a patient stops taking dapoxetine, he should wait for 7 days before receiving these drugs. The most common effects when taking dapoxetine dapoxetine 60 mg tablets are nausea, dizziness, dry mouth, headache, diarrhea, and insomnia. [16][17] Discontinuation rates due to adverse effects and costs are very high, as demonstrated in a study in Asia which showed that cumulative discontinuation rates within one year are as high as 87%. [18] Unlike other SSRIs used to treat depression, which have been associated with high incidences of sexual dysfunction,[19] dapoxetine is associated with low rates of sexual dysfunction. Formulated and compounded in pharmacy board-certified facilities. All ingredients thoroughly researched and tested for safety. "What sets Super Strut apart is our exclusive 4-in-1 formula, designed to address both the physical and mental aspects of erectile dysfunction. Each ingredient has been carefully selected and dosed to provide fast-acting, long-lasting results for enhanced performance, confidence, and satisfaction." Simal Patel, MD, Founder & CEO at Strut Health ParoxetineRx is a line of physician-prescribed, compounded oral capsules for premature ejaculation and erectile dysfunction.

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We mail you a convenient at-home lab test or you can upload your results if you have them. The results establish your baseline for tracking testosterone improvements and customizing your treatment plan.

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Health Care Professional-initiated education on U=U significantly improves patients' self-assessed sexual health, irrespective of gender. Further counseling, including mental health assessment and psychosexual therapy, remains the cornerstone of sexual dysfunction treatment for all genders. Primarily oral PDE5 inhibitors (sildenafil, tadalafil, vardenafil)* On-demand use: administer at least 30 minutes before sexual activityContinuous use: Tadalafil 5 mg daily On-demand use: administer at least 30 minutes before sexual activity *Use lower doses with boosted PIs (PI/r or PI/c): sildenafil 25 mg every 48 hours; tadalafil 5 mg as an initial dose, maximum 10 mg every 72 hours; vardenafil 2.5 mg, maximum 2.5 mg every 72 hours Consider behavioral interventions and/or psychosexual counseling, SSRIs, tricyclic antidepressants, clomipramine, and topical anesthetics Use lower doses of clomipramine and other tricyclics with boosted PIs; see Drug-drug interactions between antidepressants and ARVs Dapoxetine, a short-acting SSRI, is the only drug approved for on-demand treatment of premature ejaculation in Europe. Treatment must be maintained, as recurrence is highly likely upon discontinuation Discontinue or switch drugs contributing to delayed ejaculation (antidepressants, antipsychotics, diuretics, antiseizure medications) Treat comorbidities such as hypertension, pelvic nerve injury, or diabetic neuropathy PDE5 inhibitors (e.g., sildenafil — see DDI); benefit in women is generally less than in men Lubricants and/or hormonal therapy (topical or systemic) if pain is related to vaginal dryness Analgesics for pain associated with menstrual symptoms Topical lidocaine, capsaicin, or vestibulectomy for irreversible pain conditions Dapoxetine, sold under the brand name Priligy among others, is a selective serotonin reuptake inhibitor (SSRI) used for the treatment of premature ejaculation (PE) in men ages 18 to 64 years old. [3][4][5] Dapoxetine works by inhibiting the serotonin transporter, increasing serotonin's action at the postsynaptic cleft, and as a consequence promoting ejaculatory delay. [6] As a member of the SSRI family, dapoxetine was initially created as an antidepressant. However, unlike other SSRIs, dapoxetine is absorbed and eliminated rapidly in the body. Its fast-acting property makes it suitable for the treatment of PE, but not as an antidepressant. Originally created by Eli Lilly pharmaceutical company, dapoxetine was sold to Johnson & Johnson in 2003 and submitted as a New Drug Application to the US Food and Drug Administration (FDA) for the treatment of PE in 2004. [8] Dapoxetine is sold in several European and Asian countries, and in Mexico. In the US, dapoxetine has been in phase III development. In May 2012, US-based Furiex Pharmaceuticals reached an agreement with ALZA Corp and Janssen Pharmaceuticals to market dapoxetine in the United States, Japan, and Canada, while selling the rights to market the drug in Europe, most of Asia, Africa, Latin America, and the Middle East to Menarini.

Study Name Sample Size Results Duration
EAA (Erectile and Anxiety Association) 300 men Significant delay in ejaculation 12 weeks
International Study Group 500 men Improvement in control and satisfaction 6 months
Libido & Sexual Satisfaction Research 250 men No significant adverse effects 8 weeks

Randomized, double-blind, placebo-controlled trials have confirmed the efficacy of dapoxetine for the treatment of PE. [10] Different dosages have different impacts on different types of PE. Dapoxetine 60 mg significantly improves the mean intravaginal ejaculation latency time (IELT) compared to that of dapoxetine 30 mg in men with lifelong PE, but no difference is seen in men with acquired PE. [11] Dapoxetine, given 1–3 hours before sexual episode, prolongs IELT and increases the sense of control and sexual satisfaction in men of 18 to 64 years of age with PE. Since PE is associated with personal distress and interrelationship difficulty, dapoxetine provides help for men with PE to overcome this condition. With no drug approved specifically for treatment for PE in the US and some other countries, other SSRIs such as fluoxetine, paroxetine, sertraline, fluvoxamine, and citalopram have been used off-label to treat PE. Waldinger's meta-analysis shows that the use of these conventional antidepressants increases IELT two- to nine-fold above baseline, compared to three- to eight-fold when dapoxetine is used. [11] However, these SSRIs may need to be taken daily to achieve meaningful efficacy, and their comparatively longer half-lives increase the risk of drug accumulation and a corresponding increase of adverse effects such as reduced libido.

Measure Improvement Percentage Measurement Tool Notes
Ejaculation Control Up to 70% Patient satisfaction surveys Significant for many
Confidence During Sex 65-75% Self-report questionnaires Boosts performance perception
Partner Satisfaction 60-70% Partner feedback forms Improved intimacy

[13] Dapoxetine, though, is generally categorized as a fast-acting SSRI. It is more rapidly absorbed and mostly eliminated from the body within a few hours. These pharmacokinetics are more favorable in that they might minimize drug accumulation in the body, habituation, and side effects. Dapoxetine was initially considered unsuccessful in its intended use as an antidepressant; however, it has since been investigated as a possible aid to an approach to depression treatment focused on stress reduction, based on an animal model of depression. Dapoxetine should not be used in men with moderate to severe hepatic impairment and in those receiving CYP3A4 inhibitors such as ketoconazole, ritonavir, and telithromycin. Dapoxetine also cannot be used in patients with heart failure, permanent pacemaker, or other significant ischemic heart disease. Caution is advised in men receiving thioridazine, monoamine oxidase inhibitors, SSRIs, serotonin-norepinephrine reuptake inhibitors, or tricyclic antidepressants. If a patient stops taking one of these drugs, he should wait for 14 days before taking dapoxetine. If a patient stops taking dapoxetine, he should wait for 7 days before receiving these drugs.

Safety and tolerability

Taken as needed, dapoxetine has very mild adverse effects of decreased libido (<1%) and erectile dysfunction (<4%). No case of drug overdose has been reported during clinical trials. Many men who have PE also suffer from erectile dysfunction (ED). Treatment for these patients should consider the drug–drug interaction between dapoxetine and PDE5 inhibitors such as tadalafil (Cialis) or sildenafil (Viagra). In Dresser study (2006), plasma concentration of 24 subjects was obtained.

10. Can Dapoxetine cause drowsiness?

Half of the sample pool were treated with dapoxetine 60 mg plus tadalafil 20 mg; the other half were treated with dapoxetine 60 mg plus sildenafil 100 mg. These plasma samples were then analyzed using liquid chromatography-tandem mass spectrometry. The results showed that dapoxetine does not alter the pharmacokinetics of tadalafil or sildenafil. Alcohol does not affect the pharmacokinetics of dapoxetine when taking concurrently. The mechanism through which dapoxetine affects premature ejaculation is still unclear, but dapoxetine is presumed to work by inhibiting serotonin transporter (SERT) and subsequently increasing serotonin's action at pre- and postsynaptic receptors. The most common effects when taking dapoxetine dapoxetine 60 mg tablets are nausea, dizziness, dry mouth, headache, diarrhea, and insomnia. [16][17] Discontinuation rates due to adverse effects and costs are very high, as demonstrated in a study in Asia which showed that cumulative discontinuation rates within one year are as high as 87%.

6. Top 20 FAQs

We are driven to improve the digital healthcare experience and our team is available to help you throughout the process. Safety Information:All ingredients thoroughly researched and tested for safety. Formulated and compounded in pharmacy board-certified facilities. All ingredients thoroughly researched and tested for safety. "What sets Super Strut apart is our exclusive 4-in-1 formula, designed to address both the physical and mental aspects of erectile dysfunction.

12. Is bulk export possible?

Each ingredient has been carefully selected and dosed to provide fast-acting, long-lasting results for enhanced performance, confidence, and satisfaction." Simal Patel, MD, Founder & CEO at Strut Health ParoxetineRx is a line of physician-prescribed, compounded oral capsules for premature ejaculation and erectile dysfunction. We mail you a convenient at-home lab test or you can upload your results if you have them. The results establish your baseline for tracking testosterone improvements and customizing your treatment plan. Health Care Professional-initiated education on U=U significantly improves patients' self-assessed sexual health, irrespective of gender. Further counseling, including mental health assessment and psychosexual therapy, remains the cornerstone of sexual dysfunction treatment for all genders. [18] Unlike other SSRIs used to treat depression, which have been associated with high incidences of sexual dysfunction,[19] dapoxetine is associated with low rates of sexual dysfunction. Taken as needed, dapoxetine has very mild adverse effects of decreased libido (<1%) and erectile dysfunction (<4%).

  • The onset of dapoxetine 5mg effects is usually within 30 minutes.
  • It is not intended for daily use but before sexual activity.
  • Dapoxetine can be combined with behavioral therapy for better results.
  • Consistent use as prescribed can improve sexual confidence.
  • Patients should monitor for side effects and report them to a doctor.
  • Use caution if taking other SSRIs or medications affecting serotonin.
  • Dapoxetine is not suitable for men with heart problems or liver disease.

No case of drug overdose has been reported during clinical trials. Many men who have PE also suffer from erectile dysfunction (ED). Treatment for these patients should consider the drug–drug interaction between dapoxetine and PDE5 inhibitors such as tadalafil (Cialis) or sildenafil (Viagra).

Limitations of the study

Primarily oral PDE5 inhibitors (sildenafil, tadalafil, vardenafil)* On-demand use: administer at least 30 minutes before sexual activityContinuous use: Tadalafil 5 mg daily On-demand use: administer at least 30 minutes before sexual activity *Use lower doses with boosted PIs (PI/r or PI/c): sildenafil 25 mg every 48 hours; tadalafil 5 mg as an initial dose, maximum 10 mg every 72 hours; vardenafil 2.5 mg, maximum 2.5 mg every 72 hours Consider behavioral interventions and/or psychosexual counseling, SSRIs, tricyclic antidepressants, clomipramine, and topical anesthetics Use lower doses of clomipramine and other tricyclics with boosted PIs; see Drug-drug interactions between antidepressants and ARVs Dapoxetine, a short-acting SSRI, is the only drug approved for on-demand treatment of premature ejaculation in Europe. Treatment must be maintained, as recurrence is highly likely upon discontinuation Discontinue or switch drugs contributing to delayed ejaculation (antidepressants, antipsychotics, diuretics, antiseizure medications) Treat comorbidities such as hypertension, pelvic nerve injury, or diabetic neuropathy PDE5 inhibitors (e.g., sildenafil — see DDI); benefit in women is generally less than in men Lubricants and/or hormonal therapy (topical or systemic) if pain is related to vaginal dryness Analgesics for pain associated with menstrual symptoms Topical lidocaine, capsaicin, or vestibulectomy for irreversible pain conditions Dapoxetine, sold under the brand name Priligy among others, is a selective serotonin reuptake inhibitor (SSRI) used for the treatment of premature ejaculation (PE) in men ages 18 to 64 years old. [3][4][5] Dapoxetine works by inhibiting the serotonin transporter, increasing serotonin's action at the postsynaptic cleft, and as a consequence promoting ejaculatory delay. [6] As a member of the SSRI family, dapoxetine was initially created as an antidepressant. However, unlike other SSRIs, dapoxetine is absorbed and eliminated rapidly in the body.

8. Can I get private-label packaging?

Its fast-acting property makes it suitable for the treatment of PE, but not as an antidepressant. Originally created by Eli Lilly pharmaceutical company, dapoxetine was sold to Johnson & Johnson in 2003 and submitted as a New Drug Application to the US Food and Drug Administration (FDA) for the treatment of PE in 2004. [8] Dapoxetine is sold in several European and Asian countries, and in Mexico. In the US, dapoxetine has been in phase III development. In May 2012, US-based Furiex Pharmaceuticals reached an agreement with ALZA Corp and Janssen Pharmaceuticals to market dapoxetine in the United States, Japan, and Canada, while selling the rights to market the drug in Europe, most of Asia, Africa, Latin America, and the Middle East to Menarini. In Dresser study (2006), plasma concentration of 24 subjects was obtained. Half of the sample pool were treated with dapoxetine 60 mg plus tadalafil 20 mg; the other half were treated with dapoxetine 60 mg plus sildenafil 100 mg. These plasma samples were then analyzed using liquid chromatography-tandem mass spectrometry. The results showed that dapoxetine does not alter the pharmacokinetics of tadalafil or sildenafil. Alcohol does not affect the pharmacokinetics of dapoxetine when taking concurrently. The mechanism through which dapoxetine affects premature ejaculation is still unclear, but dapoxetine is presumed to work by inhibiting serotonin transporter (SERT) and subsequently increasing serotonin's action at pre- and postsynaptic receptors. [22] Human ejaculation is regulated by various areas in the central nervous system (CNS). These signals are passed on to the brain stem, which then is influenced by a number of nuclei in the brain such as medial preoptic and paraventricular nuclei. [24] Clement's study performed on anaesthetized male rats showed that acute administration of dapoxetine inhibits ejaculatory expulsion reflex at supraspinal level by modulating activity of lateral paragigantocellular nucleus (LPGi) neurons. These effects cause an increase in pudendal motoneuron reflex discharge (PMRD) latency, though whether dapoxetine acts directly on LPGi or on the descending pathway in which LPGi located is unclear. Dapoxetine is a white, powdery, water-insoluble substance. Taken one to three hours before sexual activity, it is rapidly absorbed in the body.

Buy Dapoxetine Tablets

[22] Human ejaculation is regulated by various areas in the central nervous system (CNS). These signals are passed on to the brain stem, which then is influenced by a number of nuclei in the brain such as medial preoptic and paraventricular nuclei. [24] Clement's study performed on anaesthetized male rats showed that acute administration of dapoxetine inhibits ejaculatory expulsion reflex at supraspinal level by modulating activity of lateral paragigantocellular nucleus (LPGi) neurons. These effects cause an increase in pudendal motoneuron reflex discharge (PMRD) latency, though whether dapoxetine acts directly on LPGi or on the descending pathway in which LPGi located is unclear. Dapoxetine is a white, powdery, water-insoluble substance.

Selection of the optimal PLGA NPs

Taken one to three hours before sexual activity, it is rapidly absorbed in the body. Its maximum plasma concentration (Cmax) is reached one to two hours after oral administration. The Cmax and AUC (area under the plasma vs. time curve) is dose dependent. The Cmax and Tm (time needed to obtain the maximum plasma concentration) after single doses of dapoxetine 30 mg and 60 mg are 297 and 498 ng/ml at 1.01 and 1.27 hours, respectively. Its maximum plasma concentration (Cmax) is reached one to two hours after oral administration.

Elective and emergency surgery

A high-fat meal does reduce the Cmax slightly, but it is insignificant. It can be taken with or without food. Dapoxetine is absorbed and distributed rapidly in the body. The mean steady-state volume is 162 L. Its initial half-life is 1.31 hours (30 mg dose) and 1.42 hours (60 mg dose), and its terminal half life is 18.7 hours (30 mg dose) and 21.9 hours (60 mg dose).

Ethics approval and consent to participate

Dapoxetine is metabolized extensively in the liver and kidney by multiple enzymes such as CYP2D6, CYP3A4, and flavin monooxygenase 1. The major product at the end of the metabolic pathway is circulating dapoxetine N-oxide, which is a weak SSRI and contributes no clinical effect. The Cmax and AUC (area under the plasma vs. time curve) is dose dependent. The Cmax and Tm (time needed to obtain the maximum plasma concentration) after single doses of dapoxetine 30 mg and 60 mg are 297 and 498 ng/ml at 1.01 and 1.27 hours, respectively. A high-fat meal does reduce the Cmax slightly, but it is insignificant. It can be taken with or without food.

Question Answer Additional Notes
Is dapoxetine safe for long-term use? Generally safe under medical supervision Long-term effects still under study
Can women take dapoxetine? No, it is not indicated for women Designed specifically for men
What should I do if I miss a dose? Usually, skip and resume normal schedule Do not double dose

Dapoxetine is absorbed and distributed rapidly in the body. The mean steady-state volume is 162 L. Its initial half-life is 1.31 hours (30 mg dose) and 1.42 hours (60 mg dose), and its terminal half life is 18.7 hours (30 mg dose) and 21.9 hours (60 mg dose).

Adverse effects

Randomized, double-blind, placebo-controlled trials have confirmed the efficacy of dapoxetine for the treatment of PE. [10] Different dosages have different impacts on different types of PE. Dapoxetine 60 mg significantly improves the mean intravaginal ejaculation latency time (IELT) compared to that of dapoxetine 30 mg in men with lifelong PE, but no difference is seen in men with acquired PE. [11] Dapoxetine, given 1–3 hours before sexual episode, prolongs IELT and increases the sense of control and sexual satisfaction in men of 18 to 64 years of age with PE. Since PE is associated with personal distress and interrelationship difficulty, dapoxetine provides help for men with PE to overcome this condition.

J. Urol.

With no drug approved specifically for treatment for PE in the US and some other countries, other SSRIs such as fluoxetine, paroxetine, sertraline, fluvoxamine, and citalopram have been used off-label to treat PE. Waldinger's meta-analysis shows that the use of these conventional antidepressants increases IELT two- to nine-fold above baseline, compared to three- to eight-fold when dapoxetine is used. [11] However, these SSRIs may need to be taken daily to achieve meaningful efficacy, and their comparatively longer half-lives increase the risk of drug accumulation and a corresponding increase of adverse effects such as reduced libido. [13] Dapoxetine, though, is generally categorized as a fast-acting SSRI. It is more rapidly absorbed and mostly eliminated from the body within a few hours. Dapoxetine is metabolized extensively in the liver and kidney by multiple enzymes such as CYP2D6, CYP3A4, and flavin monooxygenase 1. The major product at the end of the metabolic pathway is circulating dapoxetine N-oxide, which is a weak SSRI and contributes no clinical effect.

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