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CME/CE

FDA Approvals: Tadalafil for Benign Prostatic Hyperplasia

  • Authors: News Author: Robert Lowes
    CME Author: Laurie Barclay, MD
  • CME/CE Released: 10/28/2011
  • THIS ACTIVITY HAS EXPIRED FOR CREDIT
  • Valid for credit through: 10/28/2012
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Target Audience and Goal Statement

This article is intended for primary care clinicians, urologists, geriatricians, and other specialists caring for patients with benign prostatic hyperplasia with or without erectile dysfunction.

The goal of this activity is to provide medical news to primary care clinicians and other healthcare professionals in order to enhance patient care.

Upon completion of this activity, participants will be able to:

  1. Describe new US Food and Drug Administration–approved indications for use of tadalafil for treatment of benign prostatic hyperplasia, along with a combination of benign prostatic hyperplasia and erectile dysfunction, in men who have both conditions.
  2. Describe adverse effects, warnings, and precautions associated with use of tadalafil.
  3. Describe other updates for October 2011 as indicated in the prescribing information for tadalafil.


Disclosures

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Medscape, LLC, encourages Authors to identify investigational products or off-label uses of products regulated by the US Food and Drug Administration, at first mention and where appropriate in the content.


Author(s)

  • Robert Lowes

    Robert Lowes is a journalist for Medscape Medical News. A former senior editor at Medical Economics magazine and contributor to numerous healthcare publications, Robert has covered medicine from almost every conceivable angle — public policy, managed care, education, ethics, medical malpractice, information technology, billing and collections, waiting-room design, and first-degree murder. His articles have won major awards such as first place in the annual journalism competition of the National Institute for Health Care Management, and several have been republished in books. Robert also is an anthologized poet. He can be contacted at [email protected]

    Disclosures

    Robert Lowes has disclosed no relevant financial relationships.

Editor(s)

  • Brande Nicole Martin

    CME Clinical Editor, Medscape, LLC

    Disclosures

    Disclosure: Brande Nicole Martin has disclosed no relevant financial relationships.

CME Author(s)

  • Laurie Barclay, MD

    Freelance writer and reviewer, Medscape, LLC

    Disclosures

    Disclosure: Laurie Barclay, MD, has disclosed no relevant financial relationships.

CME Reviewer(s)

  • Sarah Fleischman

    CME Program Manager, Medscape, LLC

    Disclosures

    Disclosure: Sarah Fleischman has disclosed no relevant financial relationships.


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    This enduring material activity, Medscape Education Clinical Briefs, has been reviewed and is acceptable for up to 300 Prescribed credits by the American Academy of Family Physicians. AAFP accreditation begins September 1, 2011. Term of approval is for 1 year from this date. Each Clinical Brief is approved for .25 Prescribed credits. Credit may be claimed for 1 year from the date of each Clinical Brief. Physicians should claim only the credit commensurate with the extent of their participation in the activity.

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CME/CE

FDA Approvals: Tadalafil for Benign Prostatic Hyperplasia

Authors: News Author: Robert Lowes CME Author: Laurie Barclay, MDFaculty and Disclosures
THIS ACTIVITY HAS EXPIRED FOR CREDIT

CME/CE Released: 10/28/2011

Valid for credit through: 10/28/2012

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Clinical Context

Tadalafil is a phosphodiesterase-5 (PDE5) inhibitor that was approved by the US Food and Drug Administration (FDA) in 2003 to treat erectile dysfunction (ED). The FDA has now expanded the approved indications to include benign prostatic hyperplasia (BPH), either alone or in combination with ED.

The inhibition of PDE5 by tadalafil improves erectile function by increasing the amount of cyclic guanosine monophosphate in the smooth muscle of the corpus cavernosa. This action increases penile blood flow, resulting in penile erection during sexual stimulation. PDE5 inhibition also affects concentration of cyclic guanosine monophosphate in the smooth muscle of the prostate, the bladder, and their vascular supply, but the precise mechanism for reducing BPH symptoms has not been determined.

Study Synopsis and Perspective

The FDA approved tadalafil (Cialis, Eli Lilly) a PE5 inhibitor to also treat the signs and symptoms of BPH as well as a combination of BPH and ED when the conditions coincide.

Men with BPH often experience sudden urges to urinate, difficulty in starting urination, a weak urine stream, and more frequent urination, including at night. In 2 clinical trials, men with BPH who took 5 mg of tadalafil daily experienced a significant improvement in these symptoms compared with men receiving a placebo. A third study showed that men who experienced both ED and BPH and who took 5 mg of tadalafil daily had improvement in both conditions compared with a placebo group.

Scott Monroe, MD, director of the Division of Reproductive and Urologic Products in the FDA's Center for Drug Evaluation and Research, said in a press release that both BPH and ED are common disorders among older men. "Cialis offers these men another treatment option," Dr. Monroe said.

For men with BPH or ED and BPH, dosage of tadalafil is 5 mg, taken at approximately the same time every day, with or without food.

Tadalafil joins a long list of other FDA-approved drugs for BPH symptoms: finasteride (Proscar); dutasteride (Avodart); dusasteride plus tamsulosin (Jalyn); and alpha-blockers terazosin (Hytrin), doxazosin (Cardura), tamsulosin (Flomax), alfuzosin (Uroxatral), and silodosin (Rapaflo).

The agency approved tadalafil for treating ED in 2003.

The FDA advises clinicians that they should not prescribe tadalafil for men taking nitrates such as nitroglycerin because the combination may trigger an unsafe drop in blood pressure. Also, the agency does not recommend combining tadalafil with alpha-blockers for the treatment of BPH because the combination therapy has not been adequately studied, and it comes with a risk of lowering blood pressure.

Warnings and Precautions

Men with limited cardiovascular function precluding sexual activity should not use tadalafil.

Concomitant use of tadalafil with alpha-blockers, antihypertensive drugs, or 5 or more units of alcohol may cause hypotension.

The dose of tadalafil should be adjusted for men taking potent inhibitors of cytochrome P450 3A4 (CYP3A4) such as ketoconazole or ritonavir, which increase exposure to tadalafil. For once-daily use, the dose of tadalafil should not exceed 2.5 mg, and for use as needed for ED, the cumulative dose should not exceed 10 mg every 72 hours.

CYP3A4 inducers such as rifampin reduce exposure to tadalafil.

In men with a history of priapism, tadalafil should be used with caution. If an erection lasts for more than 4 hours, men taking tadalafil should seek emergency treatment.

A sudden loss of vision in 1 or both eyes in men taking tadalafil may be a sign of nonarteritic ischemic optic neuropathy (NAION). These patients should stop the drug and seek medical attention. Patients with a history of NAION should be counseled regarding the increased risk for NAION with use of tadalafil.

Men who experience sudden decrease or loss of hearing while taking tadalafil should stop the drug and seek prompt medical care.

Before prescribing tadalafil for treatment of BPH, clinicians should rule out other urologic conditions with similar symptoms.

The most often reported adverse reactions, occurring in 2% or more of patients taking tadalafil, include headache, dyspepsia, back pain, muscle pain, nasal stuffing, flushing, and limb pain.

Use in Specific Populations

Use of tadalafil is not recommended in patients with severe hepatic impairment, and dosage adjustment may be needed in patients with mild or moderate hepatic impairment.

Once-daily use of tadalafil is not recommended in patients with renal impairment requiring hemodialysis or in patients with a creatinine clearance of less than 30 mL/minute. For use in these patients as needed for ED, the dose should not exceed 5 mg every 72 hours. Dosage adjustment may be needed in patients with a creatinine clearance of 30 to 50 mL/minute.

More information on tadalafil can be found on the FDA Web site.

Laurie Barclay, MD, contributed to this synopsis.

Clinical Implications

  • The FDA has now approved daily use of tadalafil to treat urinary signs and symptoms in men with BPH. The drug may also be used to treat both BPH and ED when these conditions coexist. For daily use in BPH or BPH/ED, the dosage of tadalafil is 5 mg, taken at approximately the same time every day, with or without food.
  • Use of tadalafil with nitrates, alpha-blockers, antihypertensive drugs, or 5 or more units of alcohol may cause hypotension. Men in whom cardiovascular function is too limited to engage in sexual activity should not be given tadalafil. Potent inhibitors of CYP3A4 increase exposure to tadalafil, whereas CYP3A4 inducers such as rifampin reduce exposure to tadalafil. Before prescribing tadalafil for treatment of BPH, clinicians should rule out other urologic conditions causing similar symptoms.
  • Patients with severe hepatic impairment should not be prescribed tadalafil. Patients with mild or moderate hepatic impairment may require dosage adjustment. Patients with renal impairment requiring hemodialysis, or patients with a creatinine clearance of less than 30 mL/minute, should not use tadalafil once daily. For as-needed use, the dose should not exceed 5 mg every 72 hours. Patients with a creatinine clearance of 30 to 50 mL/minute may require dosage adjustment.

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