Medications and Sexual Function in Midlife: A Guide to Common Contributors

Clarity on how common midlife prescriptions affect intimacy helps individuals evaluate drug side effects and discuss targeted treatment adjustments with their doctors.

Share
White Reddit alien mascot face icon on transparent background.White paper airplane icon on transparent background.White stylized X logo on black background, representing the brand X/Twitter.
September 21, 2026
Sexual Wellbeing & Intimate Confidence

You start a new prescription to manage sleep, anxiety, or blood pressure. Over the following months, the medication helps your health settle. Yet you notice a subtle shift in your intimate life. Eroticism feels distant, genital sensation seems muted, or reaching orgasm requires unexpected effort.

It is easy to assume that any change in desire or response during midlife is either an inevitable sign of aging or a direct side effect of a new pill. The reality reported in medical research is far more nuanced. Sexual function relies on a delicate balance of neurological pathways, vascular circulation, hormone levels, emotional health, and relationship dynamics. When a prescription medicine enters this system, it acts alongside existing physiological shifts rather than in total isolation.

Understanding how common medications interact with adult physiology helps replace confusion with clear facts. Clinical research demonstrates that many daily treatments can influence desire, arousal, lubrication, or orgasmic timing. However, identifying a potential link does not mean you should abandon a necessary treatment. Stopping a prescribed drug abruptly can trigger serious health risks, withdrawal symptoms, or a resurgence of the underlying condition.

This guide reviews the primary medication classes associated with sexual changes in midlife. It breaks down current scientific evidence, explains how various physiological pathways operate, and provides a structured strategy for discussing your symptoms with a healthcare professional.

What clinical evidence reveals about drug-induced sexual changes

Medical literature classifies a sexual symptom as medication-associated when a noticeable shift occurs shortly after starting a drug, increasing a dose, or stopping a treatment. To meet the criteria for substance-induced or medication-induced sexual dysfunction, the symptom must cause significant personal distress or interpersonal difficulty rather than simply reflecting a shift away from a previous routine.

Clinical evidence shows that prescription drugs can alter sexual function through several distinct pathways:

  • Central nervous system signaling: Certain drugs alter neurotransmitters like serotonin, dopamine, and noradrenaline, which govern sexual motivation, excitement, and orgasmic reflexes.
  • Vascular flow: Blood pressure treatments and cardiovascular agents can alter peripheral arterial pressure and blood flow to genital tissues.
  • Endocrine suppression: Long-term therapies, including opioids or hormone-blocking agents, can alter circulating androgen or estrogen levels.
  • Autonomic nervous system inhibition: Smooth muscle relaxation and genital swelling rely on autonomic nerve signals, which cholinergic or adrenergic blockers can disrupt.

Clinical researchers distinguish between several key terms. A sexual symptom refers to any physical or subjective shift you observe, such as reduced lubrication or delayed ejaculation. Medication-associated dysfunction describes a clear clinical link between those symptoms and a drug. Treatment-emergent dysfunction refers specifically to symptoms that appear after initiating or escalating a prescription.

Research emphasizes that a medication is rarely the sole reason for a change in sexual response. An underlying health condition, such as depression, diabetes, or hypertension, can impair sexual function on its own. When a doctor evaluates these concerns, they consider the drug, the illness, and individual physiology together.

How midlife physiological changes interact with prescription drugs

Midlife brings natural shifts in hormone production, vascular health, metabolic efficiency, and tissue elasticity. Navigating these overlapping shifts is a central focus of perimenopausal and menopause transition guidance, which helps contextualize how physical changes impact daily vitality. When medical therapies are introduced during this life stage, their effects intersect with existing biological transitions.

Sexual function in adults is best understood across several distinct but connected dimensions:

  1. Desire and interest: The psychological drive, erotic thoughts, and receptivity to sexual connection.
  2. Subjective arousal: The mental feeling of sexual excitement and emotional presence.
  3. Genital response: Physical reactions, including vulvar congestion, vaginal lubrication, or penile erection.
  4. Orgasm and ejaculation: The neuromuscular release of built-up sexual tension.
  5. Comfort and sensation: The absence of pelvic pain, tissue friction, or neural numbness during activity.
  6. Overall satisfaction: The subjective feeling of closeness, pleasure, and emotional fulfillment.

During perimenopause and postmenopause, declining estrogen levels can lead to changes in vaginal tissue thickness and natural lubrication. Concurrently, natural age-related alterations in vascular tone can affect genital blood flow. If a midlife adult takes a medication that reduces central nervous system stimulation or lowers systemic blood pressure, those physiological changes can combine.

For instance, a drug that slightly decreases subjective arousal might cause minimal disruption in a 25-year-old with robust baseline tissue hydration and high baseline circulating hormones. In a 52-year-old experiencing lower tissue elasticity and intermittent sleep disruption, that same medication might make sexual activity feel uncomfortable or effortful. Recognizing these overlapping factors prevents individuals from assuming their body is failing when multiple subtle variables are at play.

How antidepressants affect midlife sexual wellbeing

Antidepressants are among the most frequently prescribed medications in midlife, and their impact on sexual response is extensively documented in psychiatric and medical literature. Sexual side effects have been reported across virtually all antidepressant categories, including selective serotonin reuptake inhibitors, serotonin-norepinephrine reuptake inhibitors, tricyclic antidepressants, monoamine oxidase inhibitors, and newer multimodal drugs.

Clinical evidence indicates that selective serotonin reuptake inhibitors and certain serotonin-norepinephrine reuptake inhibitors carry a substantial likelihood of treatment-emergent sexual changes. In primary care literature focusing on women's health, estimates of sexual side effects associated with selective serotonin reuptake inhibitors generally range between 30% and 70%. These broad estimates vary depending on whether clinical trials relied on patient self-reporting or used direct, structured questionnaires during routine follow-up visits.

Neurological mechanisms behind serotonergic effects

Elevated brain serotonin, particularly through action at specific 5-HT2 and 5-HT3 receptors, decreases central sexual drive and delays neuromuscular reflexes. At the same time, high serotonergic tone can downregulate dopamine release in brain regions that trigger sexual motivation and reward.

This physiological pattern often presents as a distinct set of experiences:

  • Spontaneous erotic thoughts and sexual desire become less frequent.
  • Subjective excitement during intimate moments feels delayed or muted.
  • Physical stimulation yields less pronounced genital sensation.
  • Reaching orgasm takes significantly longer or becomes impossible.

Despite these potential side effects, mood disorders themselves strongly suppress desire, energy, and sexual satisfaction. Managing emotional stability is vital, and exploring strategies within mental wellbeing and emotional fitness can offer valuable perspective on balancing mental health with overall quality of life. For many individuals, effective depression treatment ultimately improves intimate connection by restoring emotional capacity and reducing anxiety.

Comparing risk profiles across antidepressant options

Research demonstrates that not all psychiatric medications carry the same probability of sexual side effects. Strongly serotonergic medications like fluoxetine, paroxetine, sertraline, citalopram, and venlafaxine show higher rates of orgasmic delay and reduced desire in clinical trials.

In contrast, agents with alternative mechanisms of action display lower rates of sexual interference:

  • Bupropion: Acts primarily on dopamine and norepinephrine pathways, making it far less likely to cause orgasmic delay or libido suppression.
  • Mirtazapine: Antagonizes specific serotonin receptors that usually inhibit sexual response, resulting in a lower incidence of dysfunction.
  • Agomelatine and moclobemide: Show favorable sexual side effect profiles in comparative clinical trials due to their distinct receptor targets.

Medical guidelines emphasize that these differences do not make one drug superior for every individual. A medication that preserves sexual response may be less effective for specific panic disorders or severe clinical depression. Prescribing decisions require a careful balance between mental stability and physical comfort.

In rare instances, medical literature describes persistent post-treatment symptoms, where sexual changes remain after a serotonergic drug has been tapered and stopped. While this phenomenon is uncommon, its presence underlines why any modification to antidepressant therapy should be managed under direct medical supervision rather than attempted independently.

How cardiovascular and blood pressure medications impact function

Cardiovascular health and sexual function share a direct physiological link. Both erection and female genital arousal depend on healthy arterial dilation, strong endothelial function, and steady blood flow. Consequently, cardiovascular disease itself is a primary cause of sexual changes in midlife.

When individuals report sexual concerns after starting blood pressure therapy, identifying the root cause requires evaluating both the drug and the underlying vascular condition. High blood pressure damages blood vessel linings over time, restricting the rapid blood flow required for arousal responses.

Differing effects among antihypertensive drug classes

Clinical trials show that different blood pressure medications carry varying risks for sexual side effects:

  • Thiazide diuretics: Historically linked with higher rates of erectile difficulty and reduced genital blood flow. Some recent observational studies suggest the risk varies depending on dose and patient health.
  • Conventional beta-blockers: Frequently associated with lower sexual desire and erectile challenges. These drugs lower heart rate and reduce sympathetic nervous system activity, which can impair circulatory adjustments during physical exertion.
  • Nebivolol: A newer beta-blocker that stimulates nitric oxide release in blood vessel linings. Studies suggest it has a more favorable profile regarding erectile function compared to older beta-blockers like atenolol or propranolol.
  • ACE inhibitors and Angiotensin II Receptor Blockers: Clinical trials generally show these classes have a neutral or potentially favorable impact on sexual function by supporting endothelial health and blood vessel relaxation.
  • Calcium channel blockers: Generally classified as neutral regarding sexual side effects, though individual responses can vary.

An established long-term trial evaluating hypertension treatments found that erectile difficulty occurred more frequently in men assigned to diuretic therapy than in those assigned to placebo. However, participants taking enalapril, amlodipine, or acebutolol showed rates of sexual side effects comparable to placebo groups.

Spironolactone, a potassium-sparing diuretic with antiandrogenic properties, can block androgen receptors directly. This action can lead to reduced libido, breast tenderness, or altered arousal responses in both women and men.

Stopping blood pressure medication without a doctor's guidance invites serious health risks, including stroke, heart attack, and kidney damage. Poorly controlled hypertension causes far more severe, permanent vascular damage to sexual organs than most antihypertensive medications. A clinician can often adjust dosages or switch drug classes to preserve cardiovascular safety while resolving unwanted side effects.

How hormonal contraception and hormone treatments influence desire and comfort

Hormonal contraception is commonly used during midlife to manage irregular perimenopausal bleeding, treat conditions like endometriosis, or prevent pregnancy. Public debate around hormonal contraceptives often presents contradictory views, with some claiming these medications eliminate libido and others asserting they have no impact. Clinical evidence reveals a more nuanced reality.

A major systematic review examining 36 studies with over 13,000 participants evaluated the sexual effects of combined oral hormonal contraceptives. The analysis revealed that the vast majority of users experienced no significant change in sexual drive. Specifically:

  • 84.6% of participants reported no change in sexual desire.
  • 12.0% of participants reported an increase in sexual desire.
  • 3.5% of participants reported a decrease in sexual desire.

Position statements from leading sexual medicine societies confirm that while most individuals experience stable sexual function on combined oral contraceptives, a small minority notices clear changes in desire, arousal, lubrication, or orgasmic comfort.

Biological factors behind contraceptive effects

Combined oral contraceptives suppress pituitary gonadotropins to prevent ovulation, which lowers ovarian androgen production. They also increase sex hormone-binding globulin production in the liver, reducing the amount of free, unattached testosterone in circulation.

While free testosterone plays a role in sexual motivation and tissue sensitivity, the relationship between circulating testosterone levels and subjective desire in women is complex. A drop in free testosterone does not automatically lead to low libido.

Other factors that can influence sexual response on hormonal contraception include:

  • Progestin type: Synthetic progestins with strong antiandrogenic profiles may lower genital tissue sensitivity or natural lubrication in susceptible individuals.
  • Estrogen dosage: Low-dose estrogen formulations may result in lighter natural lubricating responses or localized vulvar dryness for certain users.
  • Psychological relief: For many individuals, removing the fear of unintended pregnancy or controlling painful periods significantly improves sexual interest and enjoyment.

Distinguishing contraception from other midlife hormonal therapies

It is important to differentiate between hormonal contraceptives used in midlife and other endocrine therapies:

  • Systemic Menopausal Hormone Therapy: Designed to replace declining estrogen during perimenopause or postmenopause, often improving lubrication, tissue elasticity, and overall comfort.
  • Local Vaginal Estrogen: Applied topically to treat genitourinary symptoms of menopause without significantly increasing systemic hormone levels or altering baseline libido.
  • Selective Estrogen Receptor Modulators and Cancer Therapies: Treatments such as tamoxifen or aromatase inhibitors suppress estrogen activity to manage breast cancer risk. These medications frequently cause vaginal dryness, painful intercourse, and reduced desire.

If you suspect your contraceptive or hormone therapy is affecting your sexual wellbeing, a healthcare provider can evaluate your current formulation, assess localized tissue health, and discuss alternative delivery methods or options.

How pain medications and chronic treatments affect intimacy

Chronic pain is a major contributor to reduced intimate connection in midlife. Persistent discomfort disrupts sleep, raises stress hormones, restricts physical mobility, and consumes emotional energy. However, medications used to manage chronic pain, particularly prescription opioids, can independently alter reproductive hormones and sexual reflexes.

Long-term prescription opioid use can cause opioid-induced androgen deficiency by suppressing the hypothalamic-pituitary-gonadal axis. Opioids bind to specific receptors in the hypothalamus, decreasing the secretion of gonadotropin-releasing hormone. This drop reduces luteinizing hormone release from the pituitary gland, leading to reduced testosterone production in both men and women.

Clinical presentation of opioid-induced endocrine changes

Medical reviews report that sexual side effects among individuals on chronic opioid therapy range widely, with estimates spanning from 20% to 80% depending on dosage, duration, and patient health. In an analysis of long-term prescription opioid users, significant sexual symptoms were reported by 76% of male participants and 64% of female participants.

Opioid-induced androgen suppression can lead to:

  • Marked reduction in sexual interest and spontaneous fantasy.
  • Difficulty achieving or maintaining erections.
  • Generalized fatigue, decreased muscle stamina, and low mood.
  • Irregular menstrual cycles or early cessation of menses.
  • Blunted genital sensation and delayed orgasmic response.

Beside endocrine suppression, opioids cause sedation and reduced central nervous system responsiveness. When combined with other sedating drugs, such as muscle relaxants or sleep aids, physical responsiveness and sexual interest are diminished further.

Managing chronic pain while protecting sexual wellbeing requires open communication with your prescribing doctor. Tapering or switching pain medications must always be performed under direct medical guidance to avoid severe pain flares or physical withdrawal.

Additional medication categories affecting sexual function

Several other drug classes commonly prescribed in midlife can alter sexual drive or physical response:

  • Antipsychotics: Drugs that block dopamine receptors can elevate prolactin levels. High prolactin lowers circulating sex hormones, frequently causing reduced desire, lubrication challenges, erectile dysfunction, or anorgasmia.
  • Antiandrogens and prostate therapies: Medications like finasteride or dutasteride block the conversion of testosterone to its active form. They can lead to lower libido, orgasmic changes, or reduced genital sensitivity.
  • Antiepileptic and mood-stabilizing agents: Certain anti-seizure medications increase liver production of sex hormone-binding globulin, reducing free hormone availability and causing sedation or reduced responsiveness.
  • Sedating antihistamines and anticholinergics: Over-the-counter and prescription allergy or sleep aids can dry mucosal membranes throughout the body, reducing vaginal lubrication and causing general lethargy.

How to evaluate sexual changes with a practical framework

Because sexual function depends on multiple overlapping systems, determining whether a medication is contributing to a physical change requires a systematic review. Rather than assuming a single prescription is entirely responsible, clinicians use structured evaluation steps to isolate potential causes.

  • PRACTICAL EVALUATION FRAMEWORK
  • 1. IDENTIFY SPECIFIC DOMAINS
  • Desire Arousal Lubrication Erection Orgasm Comfort
  • 2. ESTABLISH TIMELINE
  • Medication start date Dose changes Symptom onset
  • 3. ASSESS CONCURRENT CONTRIBUTORS
  • Hormonal status Pain Sleep Stress Vascular health
  • 4. WEIGH CLINICAL BENEFITS VS. SIDE EFFECTS
  • Disease control Quality of life Safety considerations

Key questions for evaluating your symptoms

When examining changes in your intimate health, consider these clinical evaluation questions:

  1. What specific domain has changed? Clarify whether the issue involves desire, subjective arousal, tissue lubrication, erectile capacity, orgasmic timing, or local physical discomfort.
  2. When did the symptoms begin? Compare the exact onset of the symptom with dates you started a new drug, increased a dose, or switched formulations.
  3. What concurrent health shifts occurred? Determine whether sleep disruptions, perimenopausal hot flashes, mood changes, or new joint pain began around the same time.
  4. Is the symptom constant or situational? A physical effect caused strictly by a medication usually occurs consistently across all contexts, whereas situational shifts may reflect fatigue, stress, or relationship tension.
  5. What critical benefits does the medication provide? Evaluate how well the drug controls your blood pressure, mood stability, pain, or underlying medical risk.

Illustrative clinical examples

These simplified scenarios demonstrate how different medication-related changes are evaluated in clinical practice:

  • Case Example A (Antidepressant and Orgasmic Delay): A 48-year-old woman starts a selective serotonin reuptake inhibitor for generalized anxiety. Within six weeks, her daily anxiety reduces significantly, but she notices that reaching orgasm now requires extreme effort. Her doctor confirms that the timeline aligns with serotonergic side effects. Rather than stopping the drug, they discuss adjusting the timing of her dose or considering a switch to a multimodal antidepressant.
  • Case Example B (Cardiovascular Therapy and Erectile Function): A 55-year-old man begins a conventional beta-blocker for hypertension and reports difficulty maintaining an erection two months later. His physician evaluates his overall vascular risk, checks for underlying blood sugar elevation, and transitions him to an angiotensin receptor blocker, which maintains his blood pressure control while resolving the erectile issue.
  • Case Example C (Contraceptive Switch and Local Discomfort): A 42-year-old woman switches to an antiandrogenic combined oral contraceptive to manage heavy bleeding. Four months later, she reports low desire and vulvar irritation during sex. A clinical exam reveals localized tissue dryness rather than a total loss of drive. Treating the local tissue dryness directly resolves her discomfort and restores her intimate confidence.
  • Case Example D (Chronic Pain Treatment and Endocrine Shift): A 52-year-old man taking high-dose daily opioids for chronic lower back pain reports persistent fatigue, muscle weakness, and zero interest in intimacy. Laboratory tests reveal low total and free testosterone secondary to opioid-induced pituitary suppression. His clinical team creates a plan to gradually optimize his pain regimen while managing his hormonal health.
  • Case Example E (Preserved Drive with Painful Penetration): A 57-year-old postmenopausal woman remains deeply interested in her partner but avoids sexual contact because intercourse causes sharp burning sensations. Her doctor identifies genitourinary syndrome of menopause rather than a medication side effect. Prescribing low-dose topical vaginal estrogen restores tissue elasticity and eliminates pain without altering her prescription medications.

How to prepare for a clinical medication review

If you suspect a prescription is affecting your sexual wellbeing, organizing your information before speaking with a healthcare professional ensures a productive consultation. Medical appointments are often brief, so clear preparation helps your provider understand your concerns quickly. For further guidance on maintaining overall physical vitality during midlife health evaluations, explore insights on metabolic and body composition health.

Preparing your medication preparation checklist

Before your appointment, write down details for the following ten items:

  1. Your primary physical concern: Identify whether you are experiencing reduced drive, delayed orgasm, dryness, or pain.
  2. Exact onset dates: Note when the symptom started relative to starting or changing a prescription.
  3. Complete medication list: Include all prescription drugs, over-the-counter remedies, sleep aids, and dietary supplements with current dosages.
  4. Recent dosage adjustments: Highlight any recent increases, decreases, or missed doses.
  5. Pattern of symptoms: Note whether the issue occurs during every intimate encounter or varies by circumstance.
  6. Prior baseline: Describe your typical sexual function before starting the treatment.
  7. Overall health updates: Note any shifts in mood, sleep quality, joint pain, or stress.
  8. Underlying medical diagnoses: List known conditions such as diabetes, high blood pressure, thyroid imbalance, or depression.
  9. Personal distress level: Describe how much these shifts are affecting your emotional wellbeing or relationship.
  10. Your primary health priorities: Clarify what is most important to you, such as maintaining mood stability, protecting heart health, or regaining physical comfort.

Specific questions to ask your doctor

You can guide the conversation during your review using these focused questions:

  • "Could any of my current prescriptions or over-the-counter supplements be contributing to these physical changes?"
  • "Is the condition being treated also known to cause these specific symptoms?"
  • "Are there alternative drug options in this class with a lower probability of sexual side effects?"
  • "Would adjusting the timing or dosage of my current prescription be safe and appropriate?"
  • "Are there local treatments, such as topical vaginal estrogen or physical therapy, that could help my physical comfort without changing my primary medication?"
  • "If we decide to adjust my prescription, how long will it take to see an improvement, and how will we monitor my primary health condition?"

When medical evaluation matters

While many sexual side effects can be managed during routine medical visits, certain symptoms require direct clinical attention. Sudden or severe changes in your body can indicate underlying vascular, neurological, or localized medical issues that extend beyond a standard medication side effect.

For more targeted information on managing intimate discomfort, dry tissues, or anatomical changes, consult our dedicated sexual wellbeing and intimate confidence guidance. Additionally, supporting your foundational physical health through proper midlife nutrition and physical health provides a strong base for general vitality and recovery.

Key reasons to seek prompt clinical evaluation

Schedule an appointment with a healthcare professional if you experience:

  • Severe physical pain: Pain during or after sexual activity should always be evaluated to check for infections, pelvic floor dysfunction, or dermatological conditions.
  • Unexplained bleeding: Any unexpected postmenopausal bleeding or bleeding after intercourse requires prompt medical evaluation.
  • New neurological symptoms: Numbness, weakness, tingling, or loss of pelvic sensation warrants direct clinical investigation.
  • Sudden erectile loss: Sudden erectile dysfunction can serve as an early indicator of cardiovascular disease or metabolic changes.
  • Severe mood changes: If reducing or altering a medication leads to worsening depression, severe anxiety, or panic, contact your provider immediately.

Never stop taking a prescription medication abruptly due to sexual side effects. Abruptly stopping blood pressure medications, antidepressants, pain management drugs, or anti-seizure therapies can result in dangerous physical rebound effects, severe withdrawal, or medical emergencies. All medication adjustments must be performed under the guidance of a qualified healthcare provider.

Where current scientific evidence remains limited

While medical research offers clear insights into medication side effects, important gaps remain in scientific literature regarding midlife sexual health. Recognizing these limitations helps prevent oversimplified assumptions about your health.

Primary areas where current research remains limited include:

  • Underrepresentation of midlife women: Many early cardiovascular and antihypertensive trials evaluated sexual side effects almost exclusively in men, focusing on erectile function while omitting measures of female desire, lubrication, or orgasmic response.
  • Complex confounding variables: Disentangling the side effects of a drug from the physical symptoms of the underlying condition (such as separating antidepressant side effects from clinical depression) remains challenging in observational studies.
  • Wide variation in study methodology: Clinical trials use different questionnaires, definitions, and diagnostic criteria for sexual dysfunction, making direct comparisons between individual drugs difficult.
  • Limited long-term persistent symptom data: Data regarding rare persistent post-treatment side effects following antidepressant or antiandrogen discontinuation rely primarily on observational reports, leaving true prevalence and biological mechanisms unclear.
  • Individual biological variability: Genetics, baseline hormone levels, liver metabolism, and personal relationship dynamics mean that a medication causing severe side effects in one person may have zero effect on another.

Because scientific evidence continues to evolve, clinical decisions must be tailored to your specific physical responses, health history, and personal priorities rather than broad generalizations.

The Takeaway

Changes in midlife sexual function are often complex and multifactorial, arising from an intersection of prescription medications, natural hormonal transitions, underlying health conditions, and daily stress. If you notice a shift in desire, arousal, comfort, or orgasmic response after starting or changing a medication, do not stop taking your prescribed treatment independently. Instead, schedule a comprehensive medication review with your doctor to explore safe, personalized adjustments that protect both your overall health and your intimate wellbeing.

When to revisit this resource

Revisit this guide whenever you are prescribed a new daily medication, undergo a dosage adjustment for an existing prescription, or begin noticing unexpected shifts in your physical comfort, desire, or intimate responsiveness.

Sources

  1. Management of Antidepressant-Induced Sexual Dysfunction - PMC
  2. Sexual dysfunction induced by psychotropic drugs: a narrative review
  3. Antidepressant-associated sexual dysfunction: impact, effects, and ...
  4. Sexual Dysfunction with Antidepressants: A Clinical Review
  5. Conclusion
  6. a review of the evidence for drug-induced sexual dysfunction
  7. ANTI-HYPERTENSIVES AND SEXUAL DYSFUNCTION: A LITERATURE REVIEW
  8. Anti-hypertensive medications and erectile dysfunction: focus on β ...
  9. Combined estrogen-progestin oral contraceptives and ...
  10. Erectile Dysfunction and Hypertension: Impact on ...
  11. (PDF) Reduction in genital sexual arousal varies by type of oral ...
  12. (577) Opioid-Induced Androgen Deficiency (OPIAD) With ...
  13. Opioids and Their Endocrine Effects: A Systematic Review and ...
  14. Substance/Medication-Induced Sexual Dysfunction
YOUR NEXT CHAPTER

Feel informed, strong and at home in your changing body

Keep learning about the changes that shape energy, strength, confidence and wellbeing through midlife.

Explore Resources