BPH, (Benign Prostatic Hyperplasia), or enlarged prostate is a common condition.
In fact, it is estimated that 90% of the men who live to 85 years will suffer from BPH.
A few decades ago if you had prostate problems, the only conventional medical approach would have been surgery.
However, over the last few decades, researchers have created more medical alternatives to “treat” BPH and shrink the prostate.
This variety of options available to treat BPH can often be confusing.
Many men are left questioning “which medication is right for me?” Or “is this pill safe, does it work, what are the side-effects?“.
This article will provide you with a complete, easy to understand break down of all of the commonly prescribed benign prostatic hyperplasia medications.
We will address the safety, efficacy, speed of results and long term side-effects of each drug.
We will also look at the most common alternative, natural & herbal treatments to help men with mild to severe BPH.
Different types of BPH drugs
The following is a quote from a 2007 Harvard medical panel discussion on the state of prostate medications.
“One of the most vexing issues for people with BPH is deciding whether to begin treatment for urinary difficulties and other symptoms. Studies of the natural history of BPH for up to five years show that, even without treatment, symptoms will not worsen in 16% of men, and they will actually improve in 38% of men.”
Let’s do the math: in the majority of cases (54%), men will either see no worsening symptoms or see an improvement in their symptoms, without taking prescription prostate medications.
It is only a slim one, and it still leaves 46% of men who will see their health decline if they take no action. So what are their options?
Currently, there are three types of prescription prostate drugs prescribed:
- 5-alpha-reductase inhibitors.
- phosphodiesterase-5 Inhibitors.
5-alpha-reductase inhibitors work by interfering with an enzyme called 5-alpha-reductase.
This enzyme is primarily responsible for converting testosterone to dihydrotestosterone (DHT). DHT is the hormone that causes the growth of prostatic tissue.
5-alpha-reductase inhibitors generally have more sexual side effects than other prostate medications.
They can cause decreased libido, erectile dysfunction, ejaculation problems as well as gynecomastia and various effects on mood, probably due to the way the drug interacts with testosterone levels.
It is worth noting that not all 5-alpha-reductase inhibitors are as likely to cause these side effects.
Nor would all men experience them, if you are experiencing side effects with one medication then you may wish to talk to your doctor about changing to a different drug.
The advantage of using 5-alpha reductase inhibitors is that they not only treat the symptoms of BPH but also shrink the size of hyperplastic prostate tissue – an effect that the rest of the drugs don’t have.
Notably, alpha-blockers do not directly affect the prostate in any way. Instead, they work by preventing the muscles in your prostate from contracting. They hold the bladder sphincter in a permanently relaxed state, allowing you to pass urine with greater ease.
The upside of alpha-blockers is that they work faster than 5-alpha-reductase inhibitors.
You can experience relief from symptoms in a matter of days or weeks. Whereas with 5–alpha-reductase inhibitors, the effect is slower, on average about three to six months to start working.
Additionally, some studies have shown that alpha-blockers are ineffective once the prostate gets over 40-50 grams, which means that alpha-blockers may not be suitable for severe cases of BPH.
There currently is only one phosphodiesterase-5 Inhibitor approved by the FDA to treat BPH, sold with the brand name Cialis.
If you are struggling with ED and an enlarged prostate then your doctor may prescribe you Cialis instead of other BPH medications.
Finasteride is a 5-alpha-reductase inhibitor. It prevents the enzyme 5-alpha-reductase from converting testosterone into DHT. Prostate growth and size is dependent mainly on DHT levels.
Studies have revealed that Finasteride reduces intraprostatic DHT levels by 91.4%. Making it the most effective of all 5-alpha-reductase inhibitors currently available on the market.
However, it may also be the reason that Finasteride has dose-dependent sexual side effects
Side effects of Finasteride
By lowering DHT levels, Finasteride actively decreases the size of the prostate.
This process takes at least three to six months before the clinical effects kick in.
Therefore the efficacy of Finasteride cannot be clinically appreciated until the patient has been on the medication for a substantial amount of time.
In a 4-year placebo-controlled study of 1,524 patients treated with Finasteride and 1516 patients treated with placebo were followed over a period of 4 years.
The most frequently reported adverse reactions were related to sexual function:
- 8.1 % of men reported regular impotence.
- 6.4 % of men reported decreased libido.
- 3.7% of men saw a reduced volume of ejaculate.
Less common side effects included: the growth of male breasts; tenderness, soreness, and pain in male breasts; rashes, allergic reactions, itching, hives, and swelling of the lips and face.
Some men report testicular pain, and there is a mild to moderate risk of developing male breast cancer.
Recent research also shows that the sexual and cognitive side effects of finasteride can persist for as long as ten years after men stopped taking the drug.
A 2014 meta-study coined the phrase “Post Finasteride Syndrome,” and noted that:
“Many clinicians are unaware of the scope of the persistent physical and psychological adverse effects of finasteride. Symptoms range from minor to severe.”
The meta-study examined 12 research papers that all showed high percentages (80-90+ percent) showing persistent and long-lasting sexual and psychological side effects.
A 2011 research paper had the highest percentages:
“96% of the men in the study who took finasteride experienced sexual problems lasting for more than a year after they stopped taking the drug.”
In another large scale drug report from 2017, 103 young men (16-42 years old) who were taking low dose finasteride for hair loss developed ED. In a third of them (33%), ED persisted after stopping the medication.
Studies in males with persistent sexual side effects have demonstrated that sexual dysfunction was already present before treatment with finasteride started or may respond to a psychological, and not a biological approach.
The study also noted that the longer the men took finasteride or dutasteride, the higher their risk.
Men who had taken finasteride for a period of 205 days had a 4.9-fold higher risk of Persistent Erectile Dysfunction (PED) than men with shorter exposure.
The sexual side effects of Finasteride are often the primary concern for men. However, there is also a potential risk of more aggressive prostate cancer that may be associated with Finasteride.
Multiple studies have now reported that Finasteride may reduce the incidence of prostate cancer, although these are controversial results.
It appears that Finasteride may lower your risk of developing slow-growing prostate cancers while increasing your risk of aggressive prostate cancer.
The largest study investigating prostate cancer prevention with Finasteride was published in 2003. It found a 24.8% risk reduction in the prevalence of prostate cancer over seven years.
However, it also noted an alarming increase in high-grade 7 or above tumors in the Finasteride group (37%) versus the placebo group (22%).
Despite the risks and potential side effects of Finasteride, many men still choose to take it, due to its proven efficacy.
Just after the FDA approved Finasteride, a large scale study was conducted examining its efficacy.
Eight hundred ninety-five subjects with BPH were randomized to receive a placebo or 1mg or 5 mg of Finasteride over one year (Gormley, 1992). The primary outcome measures consisted of a symptom score and a peak flow rate, although measurements of prostate size were also recorded.
The symptom score measures the total scores of nine symptoms: decreased urinary stream, dribbling, interruption in the stream, hesitancy, feeling of incomplete emptying, straining to initiate flow, urgency, incontinence, and dysuria.
The group taking the 5 mg oral dose of finasteride per day showed a statistical improvement in symptoms (21% improvement) compared with the placebo group (just 2%).
Another group taking a lower dose of finasteride (1mg oral per day) saw no statistical improvement in symptoms over the placebo group.
Further studies have demonstrated that this response is associated with prostate size at the beginning of the treatment.
Boyle et al., 1996, undertook a meta-analysis of six randomized, placebo-controlled clinical trials to provide a more thorough consensus.
The conclusion was that men with smaller prostate saw little-to-no symptomatic relief when compared to men with larger prostates.
Approximately 80% of the variation in treatment effect between studies was attributed to differences in mean prostate size. The beneficial effects are most pronounced in men with enlarged prostates (>25 mL).
In general, Finasteride seems to cause a modest improvement to BPH symptoms after being taken for 12 months.
As with all drugs, your body will react differently to other men. You may experience many or only a few side effects, or you may have a severe reaction.
You should consider the following factors when deciding whether or not to take Finasteride.
- Prostate size, as that is the most significant factor in determining whether or not Finasteride is going to be effective.
- Based on feedback from our customer support team, the primary complaint and regret from men who take Finasteride are the sexual side effects. Studies have shown that a small but significant proportion of patients experience Finasteride induced sexual dysfunction for many months or even years before they regain full or even partial sexual function
GlaxoSmithKline developed dutasteride as a competitor to Finasteride. It was patented in 1996 and approved in 2000 to treat BPH. They began selling it under the brand name Avodart.
Like Finasteride, Dutasteride is a 5-alpha-reductase inhibitor. However, whereas Finasteride inhibits type II isoenzyme of 5-alpha-reductase, Dutasteride is a dual inhibitor.
Meaning it affects both types I and types II isoforms of 5-alpha- reductase. (Type 1 is more abundant in extraprostatic tissues such as liver and spleen, whereas type II is produced more abundantly inside the prostate).
Dutasteride is also a more potent inhibitor of Type-2 than Finasteride, resulting in near-complete suppression of serum DHT in men who take this drug.
There are two notable differences between Dutasteride and Finasteride. Firstly, as a result of being a dual, high potency inhibitor, Dutasteride works a little quicker than Finasteride. Therefore, you should expect to see results sooner, (after 1 month rather than after 3).
Secondly, Dutasteride has a longer serum half-life than Finasteride, (3 to 16 hours for Finasteride and 5 weeks for Dutasteride).
The longer half-life may cause additional, adverse effects and may cause those side effects to persist for long after discontinuing the drug.
Side effects of Dutasteride
The concerns about Dutasteride are mostly the same as the concerns about Finasteride.
The primary concern about both 5 alpha-reductase inhibitors is the persistent sexual side effects.
A trial by REDUCE to study Dutasteride and Prostate Cancer concluded that there was an increased incidence of Gleason score 8-10 (high-grade) prostate cancer compared with men taking the placebo (1.0% versus the placebo group 0.5%).
In another 7-year placebo-controlled clinical trial with men taking a 5mg dose of Finasteride, similar results for Gleason score 8-10 prostate cancer were observed.
They concluded that both 5 alpha-reductase inhibitors might increase the risk of development of high-grade prostate cancer.
In terms of sexual side effects, there is no evidence of any difference in frequency or severity of sexual side effects.
Similar percentages of men report impotence, decreased libido and decreased the volume of ejaculate for both 5-alpha-reductase inhibitors.
A 2017 study in the Hormone Molecular Biology and Clinical Investigation stated:
“Findings suggest that long-term dutasteride therapy produces worsening of ED, reduced T levels and increased glucose, HbA1c and alters lipid profiles, suggesting [an] induced imbalance in metabolic function. We strongly recommend that physicians discuss with their patients these potentially serious adverse effects of long-term dutasteride therapy before instituting this form of treatment.”
Despite the risk of side effects, many doctors continue to prescribe Dutasteride and many men continue to see improvements when they take it. A 2002 study looked at the efficacy of Dutasteride at a dose of 0.5 mg taken orally per day (this is the standard dose).
This study compared 4,325 patients from three randomized, placebo-controlled trials (ARIA 3001 [United States], ARIA 3002 [United States], and ARIA 3003 [19 countries]) covering 400 sites in total.
The research concluded that the patient’s symptoms started to improve at 3 months, with significant improvements for most patients pooling around the 6 months mark.
An average 21.4% improvement in symptoms was noted at 24 months. This is in line with the 21% improvement reported at 3 years in the large scale Finasteride study mentioned earlier in this article.
The faster results may be due to the increased strength of the 5 alpha-reductase inhibiting properties of Dutasteride over Finasteride.
The study also noted a 57% reduced risk of acute urinary retention at 24 months, and the risk of BPH-related surgical interventions was 48% lower than a placebo control group.
A 2005 study also concluded that Dutasteride was effective, at shrinking the prostate. Noting that it reduces serum DHT levels by more than 90% in 2 weeks and significantly reduces prostate size in only 1 month, producing a 25% reduction in size over 2 years.
In addition, Dutasteride decreased total PSA levels by approximately 40% after 3 months of treatment and approximately 50% after 24 months of treatment.
As Finasteride and Dutasteride are both 5 alpha-reductase inhibitors, there are similar factors to consider.
- Firstly, prostate size, given this is the most significant indicator of whether or not a 5 alpha-reductase inhibitor is going to be useful for you.
- While it is faster working than Finasteride, you will still have to wait three months before seeing any symptomatic relief. You can expect an average 21% reduction in symptoms over two years.
- It also has several unpleasant quality of life side effects, primarily sexual in nature.
- Men considering taking Dutasteride should consult their doctor and then the way the potential side effects might impact their lives. They may also want to consider other natural alternatives that have fewer side effects.
Terazosin is a targeted alpha-blocker drug that was discovered in 1977 by Jaroslav Kyncl and his associates at Abbott Laboratories in Chicago.
Alpha-blocker medications work by binding to alpha-adrenergic receptors which prevent the receptor from being stimulated.
This prevents the transmission of nerve impulses and forces the smooth muscles in the prostate to relax.
Because it is targeted, Terazosin should only affect the smooth muscles around the bladder and prostate. Allowing for greater amounts of urine to flow more freely, however, it does nothing to shrink or heal the enlarged prostate.
Side effects of Terazosin
There are a number of side effects associated with Terazosin, hypotension, syncope, priapism and floppy iris syndrome.
The combined data from six placebo-controlled trials involving once-a-day administration of Terazosin at doses ranging from 1 to 20 mg reveals that despite its targeted nature, Terazosin still causes a marked lowering of blood pressure.
This can manifest as postural hypotension, and syncope (sudden loss of consciousness).
Losing consciousness as a result of low blood pressure is most likely due to rapid dosage increases or the introduction of another antihypertensive drug.
However, it can happen as an independent side effect of the medication, with no clear catalyst.
With Terazosin, the syncope episode can be followed by high heart rates of 120-160 beats per minute, meaning that this medication may not be suitable for anyone with cardiovascular health concerns.
However, in clinical trials involving 2,000 hypertensive patients treated with Terazosin, syncope was reported in only 1% of patients, (approximately).
Priapism, which is defined as penile erection sustained for hours, not relieved by sexual intercourse or masturbation, occurs in less than one in every several thousand patients taking Terazosin.
Intraoperative Floppy Iris Syndrome (IFIS) is a condition observed in patients undergoing cataract surgery that requires modification of the surgical technique.
It has been associated with patients that have past or present treatment using alpha-1 blockers. Patients that need this kind of surgery must avoid treatment with Terazosin or other alpha-blockers.
In clinical trials, 21% of the patients taking Terazosin experienced one or more of the following symptoms related to low blood pressure: dizziness, hypotension, postural hypotension, syncope, and vertigo.
Other reported side effects of Terazosin are:
- Dizziness 9.1% (of patients)
- Weakness 7.4%
- Headache 4.9%
- Somnolence 3.6%
- Tiredness 3.3%
- Flu Syndrome 2.4%
- Nasal Congestion/Rhinitis 1.9%
- Nausea 1.7%
- Dyspnea 1.7%
- Blurred Vision/Amblyopia 1.3%
- Peripheral Edema 0.9%
- Weight Gain 0.5%
A 2002 review of 17 studies involving 5,151 subjects of placebo-controlled studies with patients receiving Terazosin alone or in combination with Finasteride noted an average 37% improvement in reported symptoms. Study duration ranged from 4-52 weeks.
The improvement in the International Prostate Symptom Score (37%) and Peak urine flow rates (22%) by patients taking Terazosin was noticeable but did not differ significantly from the other alpha-blockers.
Notably, adverse side effects were generally mild but more frequent than with other alpha-blockers, which result in a two to four-fold increase in treatment discontinuation.
As with other alpha-blockers, Terazosin does not affect the prostate size.
Rather the improvement in symptoms is the result of its impact on the smooth muscle of the prostate, bladder neck and prostatic urethra.
But the static component of the obstruction (the enlarged prostate) is not affected. It is an asymptomatic treatment only.
- Terazosin’s efficacy in the treatment of BPH symptoms is similar to other alpha-blockers. But despite its targeted nature it still has potentially undesirable effects on blood pressure.
- Also, the higher rate of side effects, even mild ones, makes it a less popular choice.
- Besides the numerous side effects, the patient should keep in mind that this treatment doesn’t cure BPH and is only used to relieve symptoms.
Prazosin (Minipress) is a less commonly prescribed alpha-blocker than others in this report.
The US Food and Drug Administration (FDA) has disapproved of the use of this medication as a primary BPH treatment. It is only prescribed if the patient presents with hypertension and BPH.
It has been available since 1982 under the brand name Minipress, which is manufactured by Pfizer.
The exact mechanisms behind the blood-pressure-lowering effects of prazosin are still unknown.
However, like other alpha-blockers, Prazosin decreases the tone of the bladder sphincter and facilitates the opening of the bladder into the urethra.
This relieves the urinary symptoms associated with benign prostatic hyperplasia.
Through this effect, the symptoms of an enlarged prostate are masked, and the patient’s urinary complaints improve marginally.
Because Prazosin does not last long in the body, it needs to be taken two to three times daily.
This makes it a less preferred option than other alpha-blockers as there is always a chance the patient forgets to take a dose or is unable to take a dose at some point in the day, and their symptoms return.
Side effects of Prazosin
As with all alpha-blockers, Prazosin may cause syncope (sudden loss of consciousness).
This is due to an excessive postural hypotensive effect, although occasionally with Prazosin, the syncope episode has been preceded by a bout of severe tachycardia (abnormally fast heart rate).
These episodes usually occur within 30 to 90 minutes of the initial dose. It has also been reported in association with rapid dosage increments or the introduction of another antihypertensive drug.
Additionally, Prazosin has a well-known strong “first dose” effect, wherein the first dose causes a sudden sharp decline of blood pressure, resulting in a loss of consciousness.
For this reason, patients are often advised the first dose should be 0.5mg taken before bedtime.
Other hypotensive symptoms often associated with Prazosin are:
For this reason, it is recommended to avoid driving or performing hazardous tasks 24 hours after taking this medicine or when the dose is increased.
Prazosin has also been linked to Priapism.
If priapism is not treated immediately; it could result in penile tissue damage and permanent loss of potency.
In percentage, the most frequent negative side effects associated with Prazosin therapy are:
- Dizziness 10.3%
- Headache 7.8%
- Drowsiness 7.6%
- Lack of energy 6.9%
- Weakness 6.5%
- Palpitations 5.3%
- Nausea 4.9%
Less frequent adverse reactions which are reported to occur in 1–4% of patients are:
- orthostatic hypotension.
- blurred vision.
- reddened sclera.
- epistaxis, dry mouth, and nasal congestion.
In an open randomized study, 121 male patients were randomized to receive treatment with Prazosin, Terazosin, or Tamsulosin for 4 weeks.
There was a significant improvement in total symptom score when compared to baselines in the Prazosin, Terazosin, and
Tamsulosin groups, with 38%, 39%, and 26% respectively.
Prazosin is much less commonly prescribed for BPH.
As Prazosin is an alpha-blocker drug; its effect is limited to symptom relief, it doesn’t have any effect on the prostate size.
- The use of Prazosin therapy in the management of BPH lowers urinary symptoms but is only prescribed if the patient has high blood pressure and BPH.
- If you have been prescribed Prazosin or are considering it, you should be aware that there is very limited data from long-term, randomized trials on its long term safety and efficacy.
- There is also widespread availability of other alpha-blockers that have fewer side effects.
- This position is widely held and shared by The American Urology Association and regulatory organizations such as the US Food and Drug Administration (FDA) which disapproved the use of this medication as a primary BPH treatment.
- Its use in BPH is no longer enlisted or labeled in the pharmaceutical industry brochures of the product.
Doxazosin mesylate was introduced to the US market in 1995. It is a quinazoline manufactured by Pfizer pharmaceutical under the brand names Cardura.
Cardura is a selective α1 alpha-blocker used as an antihypertensive agent to treat high blood pressure and Benign Prostatic Hyperplasia (BPH).
As with all alpha-blockers, Doxazosin acts on the adrenergic receptors that are present in the prostatic tissue, prostatic capsule, and bladder neck.
By relaxing the smooth muscles, alpha-blockers can alleviate the symptoms of BPH such as urinary frequency, nocturia (excessive urination at night), weak stream, hesitancy and incomplete emptying of the bladder.
Nevertheless, the drug does not have any effect on the size of the enlarged prostate tissue – which is the fundamental cause of the urinary obstruction.
This α1 receptor is also present in many blood vessels and their activation causes constriction of blood vessels. Hence, the blockage of α1 receptors at this level produces vasodilation (constriction) of blood vessels and can result in a reduction in your blood pressure.
This is beneficial if you have abnormally high blood pressure and dangerous if you do not.
Due to this effect, Doxazosin is used as an antihypertensive. In some cases, this effect is greater than desired, producing side effects like hypotension (low blood pressure).
In 2000, a large trial designed to evaluate different antihypertensive medications including Doxazosin and its impact in preventing heart attacks was halted due to the recommendation of the National Heart, Lung, and Blood Institute.
This was because in the group receiving Doxazosin, a significant 25% higher rate of combined cardiovascular disease (CVD), including angina pectoris, congestive heart failure, stroke and peripheral arterial, was observed.
Furthermore, the Doxazosin group had a twofold higher rate of congestive heart failure when compared with the group receiving other medications, and there were trends in the same direction for strokes.
Despite these alarming results, the drug is still being used as an antihypertensive, and in the treatment of patients with Benign Prostatic Hyperplasia (BPH).
Side effects of Doxazosin
In addition to these concerns, Doxazosin has all of the issues associated with alpha-blockers in general, including syncope and other postural symptoms such as dizziness, lightheadedness, or vertigo.
These effects are most common with the first dose but can also occur when the dosage is increased, or if therapy is interrupted for more than a few days.
With Doxazosin, the condition of priapism (sustained erection regardless of sexual activity) is a known side effect. But the frequency of this complication is less than one in every several thousand patients.
Other adverse reactions with an incidence of less than 1% but of clinical interest are tachycardia (0.9 %; dysuria (0.5%), decreased libido (0.8%), leukopenia and thrombocytopenia.
Abnormal liver function tests, cholestasis, jaundice, and hepatitis have also been reported. Fluid retention, resulting in weight gain, may as well occur (0.8%).
There are currently 4 alpha-blockers that are FDA-approved to treat (lower urinary tract symptoms) LUTS: Doxazosin, Terazosin, Tamsulosin, and Alfuzosin.
The American Urological Association (AUA) Practice Guidelines committee reports that all of them are equally effective, causing on average a 4 to 6 point improvement in the American Urology Association symptom score.
Many patients perceive this score as a meaningful change. In addition, the improvement in maximal urinary flow rate is similar among all 4 medications.
In the group of men where BPH symptoms resulted from smooth muscle constriction rather than obstruction by excess glandular tissue, they are more likely to respond to an alpha-blocker. This leads to symptom improvement in 30-40% of patients.
Approximately 30% of patients experience at least a 30% increase in peak urinary flow rate. The usual improvement in peak urinary flow rate is 16-25%.
Patients with more severe symptoms have a greater response to treatment than those with milder symptoms. But it is not possible to predict who will respond to medication or which drug will work best for a particular patient.
A review article published in 2007 found that all four alpha-blockers were effective at relieving BPH symptoms. Men taking Doxazosin had a 14-39% improvement in relieving BPH symptoms.
A study by Pfizer (the manufacturer of Doxazosin) also reported improvements in indirect measures of obstruction, such as a maximum urine flow rate, which is significantly larger with Doxazosin (34-42%) than with the placebo (13-17 %).
However, this differs from independent studies. Fourteen randomized trials were analyzed and showed that the average magnitude of symptom improvement (International Prostate Symptom Score (IPSS) with Doxazosin typically did not achieve a level detectable by patients when compared with placebo (Timothy J Wilt).
Doxazosin, like other alpha-blockers drugs, has no effect on the prostate size or BPH. It is the asymptomatic treatment of this condition.
- A placebo-controlled study collected data from 1148 men who were receiving Doxazosin.
Overall, they showed an increase in the prostate volume by a median of 24% over an average of 4.5 years in the patients receiving Doxazosin.
- This suggests that Doxazosin is only effective until the condition worsens.
- This, combined with the potentially higher risk of strokes and cardiovascular disease, should be taken into account when deciding if you wish to take this medication.
Tamsulosin became available to the market in 1996 and was promoted as a breakthrough.
Tamsulosin is now the most commonly prescribed drug for men with symptoms of BPH and is often sold under the brand name Flomax.
Commonly reported side effects of Tamsulosin include: dizziness, nasal congestion, rhinitis, rhinorrhea, sinus congestion, seasonal allergic rhinitis, and even drowsiness.
It is highly likely that current research underestimates the number of, and seriousness, of these side effects.
The research conducted around this drug is kept from the public, providing very little information about the dangerous effects of Tamsulosin (popularly known as Flomax).
Side effects of Tamsulosin
A pharmacologist revealed in 2014 that over 75% of registered trials for Tamsulosin were hidden, which is a highly worrying statistic. Therefore, the true effects that this drug could have on your body remain unknown.
A big cause for concern is severe hypotension, which has rarely been reported in clinical trials. Alpha-blockers, especially untargeted ones such as Tamsulosin, relax the smooth muscles in the heart which leads to low blood pressure.
A cohort study involving 14,784 men that used an alpha-blocker from 2003 to 2013 were compared to an equal number of men who decided against the use of alpha-blockers, in order to examine whether alpha-blockers increased the risk of falling.
This is because it has been suggested that hypotension can result in serious falls, fractures or head injuries. The use of alpha-blockers increased fall risk by 14% compared to men that did not use alpha-blockers.
If you are going to have cataract surgery, then it is important that you avoid the use of Tamsulosin.
Tamsulosin has been shown to cause complications during cataract surgery and result in floppy eye syndrome (Pärssinen, 2006).
A Cochrane systematic review looked at the effects of Tamsulosin for BPH in 2003.
The review involved 14 studies that ranged from 1 to 6 months long. The study participants did report improvements in symptoms.
However, they also noted that men taking Tamsulosin were more likely to report dizziness, rhinitis and abnormal ejaculation compared to the placebo group. 75% of men who took a high dose of Tamsulosin (0.8 mg) reported side effects.
The authors of this review also suggested that a need for longer studies looking at the long term effects were required.
Another study published in the Journal of Urology (2008) compared the effects of Tamsulosin on BPH and its associated symptoms. 9% of the group withdrew due to adverse side effects, and 63% reported some form of side effect.
Side effects that were reported included erectile dysfunction, retrograde ejaculation, and reduced libido.
In another four year study, 27% of participants dropped out due to inadequate improvement in symptoms, while 17% dropped out due to side effects. The most common side effects were dizziness, abnormal ejaculation, asthenia, hypotension, erectile dysfunction, and headaches.
Evidence suggests that Tamsulosin is moderately effective at best. Patients taking Tamsulosin or considering taking Tamsulosin should be made aware that taking this medication means that symptoms are unlikely to go completely.
The size of the prostate is a determinant of the effectiveness of Tamsulosin. The drug is notably less effective when the prostate is larger.
Finally, it should be noted that a clear majority of the research around this drug remains unpublished. Therefore it is likely that available evidence overestimates its overall effectiveness.
- A 2008 study found that prostate size did not change, and PSA levels increased by 12.1% over two years of Tamsulosin use.
- It has also been identified as a potential carcinogen, but the studies so far do not have the proper methodology and they do not provide reliable evidence. Another side effect is macular degeneration in the form of Floppy Iris Syndrome.
Silodosin is the most recent drug developed for BPH. Development began in Japan, where it was marketed under the brand name Urief®, and launched in May 2006.
In the US, the FDA approved it in October 2008; and in 2010, the E.U. gave final approval for the drug to be sold in Europe.
Silodosin is an alpha-blocker. Like other alpha-blockers, it works by interfering with the adrenergic receptors.
Silodosin binds with high affinity to the alpha-1A subtype, which exists in high concentrations in the smooth muscle of the prostate, bladder neck, and urethra, but has less affinity for the alpha-1B subtype, which is present at higher concentrations in the smooth muscle of the circulatory system. This means it has a greater impact on BPH symptoms and a lower impact on blood pressure.
Hence, the vasodilatation and low blood pressure were often seen with other alpha-blockers that are not seen in patients who take Silodosin.
By relieving the tension, decreasing pressure and reducing urethral resistance, the symptoms of BPH are relieved. This improves dysuria (difficult urination) associated with benign prostatic hyperplasia.
While its low affinity for 1B receptors means that Silodosin has less of an impact on blood pressure, its higher affinity for 1A receptors can have an undesirable effect, most notably higher rates of sexual side effects.
Side effects of Silodosin
As Silodosin is a newer drug, there are no long term studies into its quality of life impacts so we cannot evaluate it on that basis.
However, in clinical trials, Silodosin demonstrated a low level of the reported cardiovascular and blood pressure-related side effects associated with existing alpha blocker-based BPH symptom treatments; including dizziness and first-dose syncope (fainting).
Nevertheless, postural hypotension, with or without symptoms (e.g., dizziness) may develop when beginning Silodosin treatment.
As with other alpha-blockers, patients should be cautioned about driving, operating machinery, or performing hazardous tasks when initiating therapy.
In a double-blind, placebo-controlled, 12-week clinical trial, 466 patients were given Silodosin, and 457 patients were administered a placebo. At least one treatment-emergent adverse reaction was reported by 55.2% of Silodosin treated patients and 36.8% for placebo-treated patients.
The majority (72.1%) of the adverse reactions were qualified by the investigator as mild.
A total of 6.4% of Silodosin treated patients, and 2.2% for placebo-treated patients discontinued therapy due to an adverse reaction.
Other adverse effects observed were:
- Diarrhea 2.6 %
- Headache 2.4%
- Nasopharyngitis 2.4%
- Nasal Congestion 2.1 %
The following adverse events were reported between 1%, and 2% of patients receiving Silodosin and these events occurred more frequently than with placebo:
- increased PSA
- abdominal pain
- priapism (painful erection).
This seems to suggest that Silodosin may have lower incidences of non-sexual side effects than other alpha-blockers.
It should also be noted that Intraoperative Floppy Iris Syndrome (IFIS), which is often associated with alpha-blocker treatment, seems to be less likely in patients taking Silodosin.
In a 9-month open-label safety study of Silodosin, only one case of IFIS was reported.
Due to its high affinity for 1A receptors and low affinity for 1B receptors, Silodosin seems to cause higher rates of retrograde and reduced ejaculation than other alpha-blockers.
Reduced ejaculation is caused by impaired function of the vas deferens, the duct which conveys sperm from the testicle to the urethra in a normal ejaculation process.
When 1A-adrenergic receptors are stimulated, they produce contraction of the vas deferens and sperm delivery from the testes to the urethra, producing a normal ejaculation.
However, if these alpha 1A-adrenergic receptors are blocked by the Silodosin action, the normal contraction is not produced, and sperm delivery is affected.
This is clinically manifested as a reduction in semen volume. It is a dynamic effect, and there are no alterations in sperm formation, number or function and the ability to orgasm is preserved.
This effect is reversible (within a few days) upon discontinuation of treatment.
A European trial concluded that Silodosin was effective for alleviating BPH symptoms, but no more so than other alpha-blockers. The trial included men aged 60+ years with a clinical diagnosis of benign prostatic hyperplasia with an International Prostate Symptom Score of 12 or higher.
Overall, 1036 patients were enrolled. Of these, 766 patients (77.1%) experienced an approximate 25% improvement in their total International Prostate Symptom Score.
The number of men reporting a high number of nighttime bathroom trips decreased from 85.7% to 52.4%. Half of the patients reported an improvement in frequency symptoms reported at baseline.
These results indicate that despite the much higher selectivity for Silodosin over other alpha-blockers like Tamsulosin, these drugs have reached the top of the dose-response curve and there is no way to make alpha-blockers more effective for alleviating symptoms or to achieve a more significant effect.
Silodosin, as other alpha-blockers drugs, does not affect the prostate size or BPH. It is asymptomatic treatment of the condition.
- A long-term evaluation of Silodosin has not yet been carried out. As such, there is no way to know its impact and safety over long term use.
- It is essential to keep in mind that this treatment, like many alpha-blockers, has limited effects on symptoms, and although it does not have the same blood pressure, vasodilation and hypotension effects as other alpha-blockers, it also creates problems like retrograde ejaculation.
- You should keep in mind that this treatment does not solve or cure the BPH.
- That being said, if you are concerned about blood pressure, or adverse side effects but still wish to take an alpha-blocker for your BPH symptoms, Silodosin may be the most suitable medication for you.
Over the past 30 years, the evolution of α-blocker therapy for BPH has focused primarily on improving convenience and tolerability, while at the same time treating symptoms of BPH.
This has resulted in the creation of Alfuzosin and has been relatively successful. Only a small number of men have reported severe side effects, with a moderate amount experiencing minor side effects.
Side effects of Alfuzosin
The most common side effects of Alfuzosin in clinical studies are:
- upper respiratory infection
Adverse side effects reported include :
- angina pectoris in patients with pre-existing coronary artery disease
- hepatocellular and cholestatic liver injury
- flush edema
- postural hypotension
When taking Alfuzosin, patients should be cautious about driving, operating machinery, or performing hazardous tasks, especially those with low blood pressure or who are taking antihypertensive medications or nitrates.
This is due to the possible occurrence of symptoms related to postural hypotension such as dizziness.
It must be used with caution in patients with a history of QT prolongation (a disorder of the cardiac rhythm) or those who are taking medications that prolong the QT interval.
If the patient is going through cataract surgery or any procedure involving the eyes, it is vital that they inform their ophthalmologist about the use of Alfuzosin, even if they are no longer taking it. The reason for this is Floppy Iris Syndrome (IFIS).
This is a syndrome where the iris becomes flaccid and may require the surgeon to make modifications during surgery. This syndrome is frequently present in patients receiving alpha-blockers, especially tamsulosin.
Although Alfuzosin is effective in controlling the symptoms of BPH and has fewer side effects than other drugs of its class, there are drawbacks.
Three placebo-controlled clinical trials involving 1,608 men were conducted in which the participants were administered daily doses of 10mg and 15mg of Alfuzosin. Following the trial:
- 5.7% experienced dizziness
- 3.0% upper respiratory tract infection
- 3.0% headaches
- 2.7% complained of fatigue
Other effects reported between 1% and 2% of patients included bodily pain, digestive problems, abdominal pain, dyspepsia, constipation, and nausea.
Further side effects included impotence and respiratory issues, such as bronchitis, sinusitis, and pharyngitis.
Approximately 30% of patients experienced at least a 30% increase in peak urinary flow rate.
The general improvement in maximum urinary flow rate is 16-25%. Patients with more severe symptoms have a more significant response to treatment than those with milder symptoms.
The effect of Alfuzosin treatment on prostate size has been studied in a randomized control trial in 2006.
In this study, 536 participants were randomly allocated to receive Alfuzosin or a placebo.
It was discovered that after three months, there were no significant differences in prostate size between the treatment groups and the placebo group. This is to be expected because, like all other alpha-blockers, it does not impact prostate size.
- Alfuzosin is possibly the most effective alpha-blockers with fewer side effects than its competitors. Symptomatic improvement is seen in 30-40% of the patients.
- However, the degree to which symptoms improve does not seem to vary at all, suggesting that while more men see positive results using Alfuzosin, the improvements are no more significant than if they had a positive reaction to any other alpha-blocker.
- Although Alfuzosin may have a better safety profile than drugs, it has numerous side effects that need to be considered.
- Moreover, it would be best if you kept in mind that this drug only acts to relieve symptoms; it does not cure or treat BPH. A notable downside of Alfuzosin is that it is much more expensive than other prostate medications.
What herbs or natural supplements treat BPH
However, due to the low percentage of men who have experienced relief using some of these drugs.
Natural solutions for prostate problems remain a better alternative in such cases.
While natural options can be more effective for some men and have less or even zero side effects, many men struggle to differentiate between the many different options available.
In our research, we have found that one natural supplement is far superior to all others currently available.
For men with an enlarged prostate, we only recommend Total Health For The Prostate, often alongside active surveillance.
Total Health for the Prostate is the first and only, truly complete, and clinically effective prostate supplement.
It is scientifically formulated to contain clinically significant dosages of the 23 most effective, most vital, prostate-restoring vitamins, minerals and herbal compounds in the world.
Because it’s a complete formulation, with a multifaceted approach to prostate health, it is more effective and faster working than any other supplement on the market.
Herbal ingredients, such as beta-sitosterol, are natural 5 alpha-reductase inhibitors that have been proven to improve urinary symptoms and flow, and may also work to shrink the prostate via the same mechanisms as pharmaceutical 5 alpha-reductase inhibitors – but without the nasty side effects.
Other herbal compounds such as curcumin have been shown to improve urinary symptoms such as urinary retention and urine flow in men with BPH.
Total Health For The Prostate also contains quercetin, derived from the flower buds of Japanese Sophora flowers. Laboratory studies demonstrate its anti-inflammatory properties which are highly beneficial for men with prostate disease.
Quercetin has been shown to reduce prostate-related pain and swelling and helps relieve urinary difficulties associated with prostate disease.
Total Health also contains essential minerals such as zinc, selenium, and boron. In a healthy prostate, zinc is the most abundant mineral in the prostate.
Research has revealed that men with BPH (an enlarged prostate) and cancer of the prostate typically have lower levels of zinc in the prostate compared to a healthy prostate.
Additionally, Total Health for the prostate contains selenium.
Studies have shown that men who live in areas with selenium-rich soils and eat a selenium-rich diet have lower chances of developing or dying of cancer, (prostate cancer). Other studies have shown that boron works to inhibit human cancer cell growth.
By providing a full suite of minerals in clinically significant doses, Total Health works to restore healthy prostate function and safeguard you against future prostate disease.
Total Health also contains a complete battery of the essential vitamins for your prostate.
Studies done at Georgetown University Medical Center examined the efficacy of natural products for men with BPH.
In this study, men were given a combination of beta-sitosterol, vitamin E and various other herbs, minerals, and vitamins.
The men taking the beta-sitosterol and vitamin E complex experienced significantly reduced nocturia (nighttime urination) and saw an improvement in frequency and overall symptoms.
Total Health contains all-natural Vitamin E in a clinically significant dose.
Other studies have linked vitamin D3 deficiency to an increased risk of developing prostate cancer at a younger age. Lab studies have shown that prostate cancer cells treated with vitamin D3 can be killed and prevented from spreading.
Total Health provides a high dose of vitamin D3 to ensure you have adequate vitamin D3 levels. Studies have also linked vitamin C to a lower risk of prostate cancer.
Is it safe?
Total Health for the Prostate contains clinically significant dosages that have shown to be safe in clinical studies.
All ingredients are 100% natural, GMO-free, and tested for contaminants, heavy metals, and radiation.
We rigorously test all raw ingredients in our products to ensure they meet the American pharmacological standards and the American herbal products association standards.
Our manufacturing facilities are all US-based and FDA-monitored. We verify the purity of our products and label accuracy using 3rd party independent laboratories.
Total Health for the Prostate is safe to take alongside all common prostate medications or supplements.
*Vitamin D3 can interact with some blood thinners. If you are taking prescription-strength blood thinners, you may wish to consult your doctor before taking Total Health for the Prostate.
Does Total Health alleviate symptoms?
Each one of the 23 nutrients has dozens of peer-reviewed, clinical research that demonstrates their efficacy and safety.
On top of that, Total Health for the Prostate has a 20-year track record of alleviating symptoms. It is backed up by hundreds of case studies, customer testimonials and review videos.
Does Total Health shrink and heal the prostate?
Unlike prescription drugs, Total Health for the Prostate is designed to shrink the prostate gland.
Ingredients such as beta-sitosterol are natural 5 alpha-reductase inhibitors, which have been shown to shrink the prostate gland.
Total Health conclusion
Total Health for the Prostate is by far the best quality and most effective natural supplement for prostate disease, BPH and general urinary health available on the market.
It contains higher dosages, more ingredients, and the most bioavailable forms of vital nutrient compounds. It is made in the USA at FDA-audited facilities and tested at 3rd party labs.
We recommend that you take Total Health for at least 90 days to combat BPH and restore prostate health. Total Health will restore prostate health naturally, as well as safeguard you against future prostate disease.
Total Health for the Prostate is a high quality, fast working, and effective all-natural prostate supplement. It works as effectively as pharmaceutical products to alleviate symptoms and reduce prostate volume and size.
However, the critical difference is that Total Health uses all-natural ingredients. As such, no side effects are experienced.
It has a 20-year track record of working effectively, backed up by the testimonies of hundreds of men from all over the world. If you would like more information about Total Health For the Prostate, Click Here.