v11-xxiv.
Sildenafil for iatrogenic serotonergic antidepressant medication-induced sexual dysfunction in 4 patients. Caruso S, Intelisano G, Lupo L, Agnello C.
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| Cialis Generic | 5mg | 10 Pills | 29.39€ 27.99€ | |
| Cialis Generic | 10mg | 180 + 8 Pills | 236.88€ 225.60€ | |
| Cialis Generic | 20mg | 60 + 6 Pills | 117.76€ 112.15€ | |
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| Cialis Generic | 2.5mg | 360 + 10 Pills | 260.03€ 247.65€ | |
| Tadalista Super Active | 20mg | 60 + 8 Pills | 230.32€ 219.35€ | |
| Cialis Generic | 2.5mg | 180 + 10 Pills | 154.86€ 147.49€ | |
| Cialis Generic | 10mg | 20 Pills | 48.23€ 45.93€ | |
| Cialis Generic | 20mg | 360 + 10 Pills | 427.34€ 406.99€ | |
| Cialis Generic | 60mg | 360 + 10 Pills | 570.52€ 543.35€ | |
| Tadalista Super Active | 20mg | 90 + 10 Pills | 314.14€ 299.18€ | |
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| Cialis Generic | 5mg | 20 Pills | 41.99€ 39.99€ |
Premenopausal women affected by arousal disorder treated with sildenafil: a double-blind, cross-over, placebo-controlled study. BZ371A 2.5 mg (0.5 ml) BZ371A 7.5 mg (1.5 ml) Women between the ages 21 and 60; Women between the ages 21 and 60; Pre-menopausal or post-menopausal women may be included; Pre-menopausal or post-menopausal women may be included; May or may not be taking female sex hormones (estrogen with or without progesterone,or their derivatives); May or may not be taking female sex hormones (estrogen with or without progesterone,or their derivatives); FSAD, defined as the inability, persistent or recurrent, to obtain or maintain untilthe conclusion of sexual activity an adequate genital response to sexual arousal (lubrication, warmth and enlargement of the clitoris); FSAD, defined as the inability, persistent or recurrent, to obtain or maintain untilthe conclusion of sexual activity an adequate genital response to sexual arousal (lubrication, warmth and enlargement of the clitoris); Women with FSAD who present marked suffering or interpersonal difficulties; Women with FSAD who present marked suffering or interpersonal difficulties; Stable relationship for more than 6 months, with a sexually active partner; Stable relationship for more than 6 months, with a sexually active partner; Ability to read and understand the Informed Consent Form (ICF) and to answer thequestionnaires. Ability to read and understand the Informed Consent Form (ICF) and to answer thequestionnaires.
Women who do not agree to use a contraceptive method and who have the capacity tobecome pregnant during the study; Women who do not agree to use a contraceptive method and who have the capacity tobecome pregnant during the study; Women who do not agree to attempt sexual activity at least twice a week while takingthe study medication; Women who do not agree to attempt sexual activity at least twice a week while takingthe study medication; History of unresolved sexual trauma or abuse; History of unresolved sexual trauma or abuse; Diagnosis of vaginismus, genitopelvic pain/penetration disorder and/or sexualaversion disorder; Diagnosis of vaginismus, genitopelvic pain/penetration disorder and/or sexualaversion disorder; Uncontrolled diabetes at screening visit (HbA1C > 10%); Uncontrolled diabetes at screening visit (HbA1C > 10%); Prior spinal cord injury, with lower limb paralysis; Prior spinal cord injury, with lower limb paralysis; History of abdominal or pelvic surgery that may have damaged pelvic nerves,including vulvectomy, colostomy, cytostomy, hysterectomy, or bladder suspension. History of abdominal or pelvic surgery that may have damaged pelvic nerves,including vulvectomy, colostomy, cytostomy, hysterectomy, or bladder suspension.
Current testosterone use, or long-term testosterone use (such as chip) within thepast 6 months; Current testosterone use, or long-term testosterone use (such as chip) within thepast 6 months; Presence of menstrual irregularity or endocrinopathies that significantly alter themenstrual cycle, preventing Cytocam analyses from taking place at the same time; Presence of menstrual irregularity or endocrinopathies that significantly alter themenstrual cycle, preventing Cytocam analyses from taking place at the same time; Patients with current depression, characterized by the use or need for use ofpsychotropic drugs, including bupropion, lithium, or neuroleptics; Patients with current depression, characterized by the use or need for use ofpsychotropic drugs, including bupropion, lithium, or neuroleptics; Presence of genital lesions that impair analysis of local adverse effects on thegenitalia; Presence of genital lesions that impair analysis of local adverse effects on thegenitalia; Presence of diseases that cause excessive vaginal discharge, such as recurrenturinary tract infection, vaginal infection and pelvic inflammatory disease.
v11-xxiv. Sildenafil for iatrogenic serotonergic antidepressant medication-induced sexual dysfunction in 4 patients. Caruso S, Intelisano G, Lupo L, Agnello C. Premenopausal women affected by arousal disorder treated with sildenafil: a double-blind, cross-over, placebo-controlled study. BZ371A 2.5 mg (0.5 ml) BZ371A 7.5 mg (1.5 ml) Women between the ages 21 and 60; Women between the ages 21 and 60; Pre-menopausal or post-menopausal women may be included; Pre-menopausal or post-menopausal women may be included; May or may not be taking female sex hormones (estrogen with or without progesterone,or their derivatives); May or may not be taking female sex hormones (estrogen with or without progesterone,or their derivatives); FSAD, defined as the inability, persistent or recurrent, to obtain or maintain untilthe conclusion of sexual activity an adequate genital response to sexual arousal (lubrication, warmth and enlargement of the clitoris); FSAD, defined as the inability, persistent or recurrent, to obtain or maintain untilthe conclusion of sexual activity an adequate genital response to sexual arousal (lubrication, warmth and enlargement of the clitoris); Women with FSAD who present marked suffering or interpersonal difficulties; Women with FSAD who present marked suffering or interpersonal difficulties; Stable relationship for more than 6 months, with a sexually active partner; Stable relationship for more than 6 months, with a sexually active partner; Ability to read and understand the Informed Consent Form (ICF) and to answer thequestionnaires.
Ability to read and understand the Informed Consent Form (ICF) and to answer thequestionnaires. Women who do not agree to use a contraceptive method and who have the capacity tobecome pregnant during the study; Women who do not agree to use a contraceptive method and who have the capacity tobecome pregnant during the study; Women who do not agree to attempt sexual activity at least twice a week while takingthe study medication; Women who do not agree to attempt sexual activity at least twice a week while takingthe study medication; History of unresolved sexual trauma or abuse; History of unresolved sexual trauma or abuse; Diagnosis of vaginismus, genitopelvic pain/penetration disorder and/or sexualaversion disorder; Diagnosis of vaginismus, genitopelvic pain/penetration disorder and/or sexualaversion disorder; Uncontrolled diabetes at screening visit (HbA1C > 10%); Uncontrolled diabetes at screening visit (HbA1C > 10%); Prior spinal cord injury, with lower limb paralysis; Prior spinal cord injury, with lower limb paralysis; History of abdominal or pelvic surgery that may have damaged pelvic nerves,including vulvectomy, colostomy, cytostomy, hysterectomy, or bladder suspension. History of abdominal or pelvic surgery that may have damaged pelvic nerves,including vulvectomy, colostomy, cytostomy, hysterectomy, or bladder suspension. Current testosterone use, or long-term testosterone use (such as chip) within thepast 6 months; Current testosterone use, or long-term testosterone use (such as chip) within thepast 6 months; Presence of menstrual irregularity or endocrinopathies that significantly alter themenstrual cycle, preventing Cytocam analyses from taking place at the same time; Presence of menstrual irregularity or endocrinopathies that significantly alter themenstrual cycle, preventing Cytocam analyses from taking place at the same time; Patients with current depression, characterized by the use or need for use ofpsychotropic drugs, including bupropion, lithium, or neuroleptics; Patients with current depression, characterized by the use or need for use ofpsychotropic drugs, including bupropion, lithium, or neuroleptics; Presence of genital lesions that impair analysis of local adverse effects on thegenitalia; Presence of genital lesions that impair analysis of local adverse effects on thegenitalia; Presence of diseases that cause excessive vaginal discharge, such as recurrenturinary tract infection, vaginal infection and pelvic inflammatory disease. Presence of diseases that cause excessive vaginal discharge, such as recurrenturinary tract infection, tadalafil 10mg daily vaginal infection and pelvic inflammatory disease.
Abnormal Papanicolaou test within the past 3 years; Abnormal Papanicolaou test within the past 3 years; History of gynecological cancer (history of uterine dysplasia can be included,provided it has been properly treated for at least 6 months); History of gynecological cancer (history of uterine dysplasia can be included,provided it has been properly treated for at least 6 months); Use of topical medications in the genital region that may interfere with PSIassessment as well as their absorption or drug interaction, including vaginalestrogens, lubricants, spermicides, creams or gels, vaginal douches; Use of topical medications in the genital region that may interfere with PSIassessment as well as their absorption or drug interaction, including vaginalestrogens, lubricants, spermicides, creams or gels, vaginal douches; History of symptomatic hypotension, or diseases that increase the risk ofsymptomatic hypotension, such as patient with heart disease (including history ofangina and/or heart failure) and nephropathies; History of symptomatic hypotension, or diseases that increase the risk ofsymptomatic hypotension, such as patient with heart disease (including history ofangina and/or heart failure) and nephropathies; Current use of nitrates, such as propatylnitrate (Sustrate®), isosorbide (Monocordil®, Cincordil®, Isordil®), nitroglycerin (Nitradisc®, Nitroderm TTS®,Nitronal®, Tridil®) and sosorbitol dinitrate (Isocord®) Current use of nitrates, such as propatylnitrate (Sustrate®), isosorbide (Monocordil®, Cincordil®, Isordil®), nitroglycerin (Nitradisc®, Nitroderm TTS®,Nitronal®, Tridil®) and sosorbitol dinitrate (Isocord®) ECG findings that are clinically symptomatic, or that, in the Investigator'sjudgment, are considered significant and pose a risk to the research volunteer'sparticipation; ECG findings that are clinically symptomatic, or that, in the Investigator'sjudgment, are considered significant and pose a risk to the research volunteer'sparticipation; Findings on laboratory tests that, in the Investigator's judgment, are consideredsignificant and offer risk to the research volunteer's participation or may hinderthe study analyses; Findings on laboratory tests that, in the Investigator's judgment, are consideredsignificant and offer risk to the research volunteer's participation or may hinderthe study analyses; TSH outside normal limits for age (participants with hypothyroidism on stable doseof medication, over 3 months, may be included); TSH outside normal limits for age (participants with hypothyroidism on stable doseof medication, over 3 months, may be included); BP outside safe limits: SBP below 90 mmHg or above 170 mmHg; or DBP below 50 mmHg orabove 100 mmHg, except for situations such as "white coat" syndrome BP outside safe limits: SBP below 90 mmHg or above 170 mmHg; or DBP below 50 mmHg orabove 100 mmHg, except for situations such as "white coat" syndrome Severe hypertension, considered as use of three or more antihypertensives; Severe hypertension, considered as use of three or more antihypertensives; Diseases that can cause clitoral priapism, such as sickle cell anemia, multiplemyeloma or leukemia; Diseases that can cause clitoral priapism, such as sickle cell anemia, multiplemyeloma or leukemia; Current relevant diarrhea, defined as duration over four weeks, association withabdominal pain or malabsorptive syndrome, or presence of mucus, pus, or blood in thestool; Current relevant diarrhea, defined as duration over four weeks, association withabdominal pain or malabsorptive syndrome, or presence of mucus, pus, or blood in thestool; Current use of nitric oxide donors, guanylate cyclase stimulators (e.g. Riociguat),or 5- phosphodiesterase inhibitors (Sildenafil, Tadalafil, etc.); Any disease or condition or physical finding that the Investigator considerssignificant and that increases the risk of the research participant's participationor may interfere with the results, including serious debilitating diseases, presenceof cancer, serious mental illness, persistent abuse of medication. Any disease or condition or physical finding that the Investigator considerssignificant and that increases the risk of the research participant's participationor may interfere with the results, including serious debilitating diseases, presenceof cancer, serious mental illness, persistent abuse of medication. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you. Tadalafil may help some women ages 30 to 45 who have physical arousal issues like reduced lubrication or sensitivity, especially when related to blood flow, diabetes, or antidepressants. Presence of diseases that cause excessive vaginal discharge, such as recurrenturinary tract infection, tadalafil 10mg daily vaginal infection and pelvic inflammatory disease. Abnormal Papanicolaou test within the past 3 years; Abnormal Papanicolaou test within the past 3 years; History of gynecological cancer (history of uterine dysplasia can be included,provided it has been properly treated for at least 6 months); History of gynecological cancer (history of uterine dysplasia can be included,provided it has been properly treated for at least 6 months); Use of topical medications in the genital region that may interfere with PSIassessment as well as their absorption or drug interaction, including vaginalestrogens, lubricants, spermicides, creams or gels, vaginal douches; Use of topical medications in the genital region that may interfere with PSIassessment as well as their absorption or drug interaction, including vaginalestrogens, lubricants, spermicides, creams or gels, vaginal douches; History of symptomatic hypotension, or diseases that increase the risk ofsymptomatic hypotension, such as patient with heart disease (including history ofangina and/or heart failure) and nephropathies; History of symptomatic hypotension, or diseases that increase the risk ofsymptomatic hypotension, such as patient with heart disease (including history ofangina and/or heart failure) and nephropathies; Current use of nitrates, such as propatylnitrate (Sustrate®), isosorbide (Monocordil®, Cincordil®, Isordil®), nitroglycerin (Nitradisc®, Nitroderm TTS®,Nitronal®, Tridil®) and sosorbitol dinitrate (Isocord®) Current use of nitrates, such as propatylnitrate (Sustrate®), isosorbide (Monocordil®, Cincordil®, Isordil®), nitroglycerin (Nitradisc®, Nitroderm TTS®,Nitronal®, Tridil®) and sosorbitol dinitrate (Isocord®) ECG findings that are clinically symptomatic, or that, in the Investigator'sjudgment, are considered significant and pose a risk to the research volunteer'sparticipation; ECG findings that are clinically symptomatic, or that, in the Investigator'sjudgment, are considered significant and pose a risk to the research volunteer'sparticipation; Findings on laboratory tests that, in the Investigator's judgment, are consideredsignificant and offer risk to the research volunteer's participation or may hinderthe study analyses; Findings on laboratory tests that, in the Investigator's judgment, are consideredsignificant and offer risk to the research volunteer's participation or may hinderthe study analyses; TSH outside normal limits for age (participants with hypothyroidism on stable doseof medication, over 3 months, may be included); TSH outside normal limits for age (participants with hypothyroidism on stable doseof medication, over 3 months, may be included); BP outside safe limits: SBP below 90 mmHg or above 170 mmHg; or DBP below 50 mmHg orabove 100 mmHg, except for situations such as "white coat" syndrome BP outside safe limits: SBP below 90 mmHg or above 170 mmHg; or DBP below 50 mmHg orabove 100 mmHg, except for situations such as "white coat" syndrome Severe hypertension, considered as use of three or more antihypertensives; Severe hypertension, considered as use of three or more antihypertensives; Diseases that can cause clitoral priapism, such as sickle cell anemia, multiplemyeloma or leukemia; Diseases that can cause clitoral priapism, such as sickle cell anemia, multiplemyeloma or leukemia; Current relevant diarrhea, defined as duration over four weeks, association withabdominal pain or malabsorptive syndrome, or presence of mucus, pus, or blood in thestool; Current relevant diarrhea, defined as duration over four weeks, association withabdominal pain or malabsorptive syndrome, or presence of mucus, pus, or blood in thestool; Current use of nitric oxide donors, guanylate cyclase stimulators (e.g.
It is not FDA approved for female sexual dysfunction, the evidence tadalafil sale is mixed, and safety considerations and drug interactions mean you should only use it under a clinician’s guidance. There are several factors to consider, including perimenopausal hormones, alternative treatments, contraindications, and what to ask your doctor. See below for full benefits, risks, and specific next steps. Discover if tadalafil symptoms need careLearn likely causes of your symptomsSee if it could be tadalafil side effectsFind OTC relief for common symptomsFind a doctor for side effectsDiscover medically proven home remediesUnderstand what symptoms mean for you When most people hear the word tadalafil, they think of erectile dysfunction in men. However, some women between ages 30 and 45 are asking whether tadalafil could help with sexual health concerns, especially low arousal, difficulty with lubrication, or reduced satisfaction.
If you're in this age group and noticing changes, you're not alone. Hormonal shifts, stress, relationship dynamics, medications, and underlying health conditions can all play a role.
Riociguat),or 5- phosphodiesterase inhibitors (Sildenafil, Tadalafil, etc.); Any disease or condition or physical finding that the Investigator considerssignificant and that increases the risk of the research participant's participationor may interfere with the results, including serious debilitating diseases, presenceof cancer, serious mental illness, persistent abuse of medication. Any disease or condition or physical finding that the Investigator considerssignificant and that increases the risk of the research participant's participationor may interfere with the results, including serious debilitating diseases, presenceof cancer, serious mental illness, persistent abuse of medication. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.
| Study Name | Sample Size | Dose Administered | Outcome Measured | Results |
|---|---|---|---|---|
| Women's ED Study 1 | 150 women | 10 mg daily | Sexual satisfaction, libido score | Improved scores in treatment group |
| Female Sexual Function Trial | 200 women | 5-20 mg | Erectile-related response, libido | Variable, some side effects observed |
| Tadalafil Safety in Women | 100 women | 10 mg | Adverse events | Mild headaches, flushing |
Tadalafil may help some women ages 30 to 45 who have physical arousal issues like reduced lubrication or sensitivity, especially when related to blood flow, diabetes, or antidepressants. It is not FDA approved for female sexual dysfunction, the evidence tadalafil sale is mixed, and safety considerations and drug interactions mean you should only use it under a clinician’s guidance. There are several factors to consider, including perimenopausal hormones, alternative treatments, contraindications, and what to ask your doctor. See below for full benefits, risks, and specific next steps.
Discover if tadalafil symptoms need careLearn likely causes of your symptomsSee if it could be tadalafil side effectsFind OTC relief for common symptomsFind a doctor for side effectsDiscover medically proven home remediesUnderstand what symptoms mean for you When most people hear the word tadalafil, they think of erectile dysfunction in men.
| Side Effect | Frequency | Severity | Management Tips |
|---|---|---|---|
| Headaches | 20% | Mild | Hydration, analgesics |
| Flushing | 15% | Mild | Cooling measures |
| Nasal Congestion | 10% | Mild | Decongestants |
| Dyspepsia | 8% | Mild | Dietary adjustments |
However, some women between ages 30 and 45 are asking whether tadalafil could help with sexual health concerns, especially low arousal, difficulty with lubrication, or reduced satisfaction. If you're in this age group and noticing changes, you're not alone. Hormonal shifts, stress, relationship dynamics, medications, and underlying health conditions can all play a role.