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Phosphodiesterase V Inhibitors

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Historical treatments for Erectile Dysfunction before the PDE5 inhibitors ... Tadalafil (Cialis) Doses: ... Back pain--unique to Cialis. Myalgia. Can be very ... – PowerPoint PPT presentation

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Title: Phosphodiesterase V Inhibitors


1
Phosphodiesterase V Inhibitors
  • By Lydia Zou
  • lzou_at_u.washington.edu
  • Doctor of Pharmacy Candidate
  • Class of 2008

2
Goals
  • Historical treatments for Erectile Dysfunction
    before the PDE5 inhibitors were discovered
  • General overview of the three drugs currently
    available today
  • Discuss the mechanism of action
  • Discuss the use of each drug (dosing, duration of
    action, etc)
  • List the side effects common and unique to all
    three drugs
  • Discuss the metabolism pathway(s) for each of the
    drugs
  • Discuss the interactions seen

3
History
  • Penile Implants (1973)
  • These are surgically implanted
  • They are still used in patients who have failed
    on other therapies
  • Overall patient-partner satisfaction is 90
  • Vascular Surgery (1973)
  • Not done very much these days (its a last
    resort)
  • Vacuum Pump (1983)
  • They work by creating a negative vacuum pressure.
    There is a constriction ring that is placed at
    the base of the penis to prevent venous drainage
    and maintain rigidity.
  • Good in theory but not in reality b/c it was
    clumsy to use

4
History
  • Vasoactive Intracavernosal pharmacotherapy
    (1995)
  • There are 2 products approved by the FDA
  • Caverject (alprostadil injection)
  • Edex (alprostadil injection)
  • Transurethral alprostadil (1997)
  • MUSE Medicated Urethral System for Erection
  • Its a small stick with aprostadil (PGE1) at the
    end that is stuck into the urethra. A release
    button is pushed to release the medication.
  • Oral PDE-5 Inhibitors (1998)

5
PDE 5 Inhibitors
  • Three drugs are currently approved
  • Sildenafil (Viagra)
  • Doses 25mg, 50mg, 100mg
  • Most patients start at 50mg and it can be taken
    anytime from 1/2 to 4 hours before sexual
    activity
  • Max frequency is once per day
  • Maybe best to take it on an empty stomach
  • Vardenafil (Levitra)
  • Doses 2.5mg, 5mg, 10mg, and 20mg
  • Most patients start at 10mg taken 60minutes
    before sexual activity
  • High fat meals can reduce the plasma
    concentration by 18-50 (on an empty stomach is
    not a bad idea)
  • Tadalafil (Cialis)
  • Doses 5mg, 10mg, 20mg
  • Most patients start on 10mg and it can be taken
    without regard to food
  • Maximum dosing frequency is once per day

6
Mechanism of Action
  • They inhibit phosphodiesterase V, which is
    responsible for the breakdown of cGMP
  • cGMP relaxes the smooth muscle and increases
    blood flow to the corpus cavernosum.
  • Note These drugs do not cause a chemical
    erection. Sexual stimulation is still needed to
    cause the initial release of nitric oxide, which
    stimulates the synthesis of cGMP.

7
Side Effects
  • Sildenafil
  • Headache and flushing
  • Dyspepsia
  • Nasal congestion
  • Abnormal vision (blue halo around lights)

8
Side Effects
  • Vardenafil
  • Headache and flushing
  • Rhinitis
  • Dyspepsia
  • Flu syndrome

9
Side Effects
  • Tadalafil
  • Headache and flushing
  • Dyspepsia
  • Nasal congestion
  • Back pain--unique to Cialis
  • Myalgia
  • Can be very bad (cant move). Pt will need to
    stop and use an alternative treatment.

10
Side Effects
  • Non-arteritic Ischemic Optic Neuropathy
  • This is the most common optic nerve disease for
    adults 50 years old
  • The onset is sudden and patients usually
    experience decreased vision in one eye
  • Occurs most frequently in the morning when first
    waking up
  • Risk Factors
  • Ischemic heart disease
  • HTN
  • Hypercholesterolemia
  • Diabetes
  • Age

11
Metabolism Pathways
  • Sildenafil
  • Major pathway 3A4 (79)
  • Minor pathways 2C9 (20)
  • 2C19 and 2D6 (
  • Vardenafil
  • Major pathway 3A4
  • Minor pathways 3A5 and 2C9
  • Tadalafil
  • Major pathway 3A4

12
Drug-Drug Interactions for the PDE 5 Inhibitors
13
Contraindications for PDE 5 Therapy
  • Nitrates
  • Patients using nitrates regularly or
    intermittently should not use any of the PDE-5
    Inhibitors.
  • Applies for any form of nitrates (sublingual,
    transdermal, etc)
  • Patients can get extreme hypotension
  • Hypersensitivity to any of the components of the
    tablet.

14
Use with Caution
  • Alpha-Blockers
  • In the past these drugs were contraindications,
    but recent evidence suggests that they can be
    used together
  • Patients should be stabilized on either the
    alpha-blocker or the PDE-5 inhibitor first before
    the other is added on at the lowest possible dose.

15
Interactions Already in the System
  • Sildenafil
  • Drug-Class Interactions
  • CYP3A4 potent Inhibitors 5 fold inc AUC
  • Potassium sparing diuretics
  • Loop diuretics
  • Antacids

16
Sildenafil contd
  • Drug-Drug Interactions
  • Amiodarone
  • Amlopdipine
  • Aspirin
  • Atazanavir
  • Bosentan
  • Cimetidine
  • Ciprofloxacin
  • Clarithromycin
  • Darunavir/ritonavir
  • Delavirdine
  • Erythromycin
  • Fluvoxamine
  • Grapefruit juice
  • Indinavir
  • Nelfinavir
  • Ritonavir (initially)
  • S-warfarin
  • Saquinavir
  • Saquinavir/ritonavir
  • tacrolimus

17
Interactions Already in the System
  • Vardenafil
  • Drug-Drug Interactions
  • Atazanavir
  • Cimetidine
  • Darunavir/ritonavir
  • Erythromycin
  • Ketoconazole
  • Ritonavir (initially)

18
Interactions Already in the System
  • Tadalafil
  • Drug Class Interactions
  • CYP3A4 Potent Inhibitors 5 fold inc AUC
  • Angiotensin Receptor Blocker and Thiazide Combos
  • Antacids

19
Tadalafil contd
  • Drug-Drug Interactions
  • Amlodipine
  • Aspirin
  • Atazanavir
  • Bendrofluazide
  • Darunavir/ritonavir
  • Doxazosin
  • Enalapril
  • Ethanol-acute
  • Ketoconazole
  • Lovastatin
  • Midazolam
  • Rifampin
  • S-warfarin
  • Tamsulosin
  • Theophylline

20
Interactions I Added
21
Sildenafil
  • Drug-Class Interactions
  • Beta-Blockers
  • The product insert states that the AUC of the
    active metabolite, N-desmethylsildenafil, was
    increased by 102 when taken with non-specific
    beta-blockers
  • Drug-Drug Interactions
  • Ambrisentan
  • A negative trial, cited in the product insert of
    ambrisentan, on healthy volunteers showed that
    sildenafil and ambrisentan did not have a
    clinically relevant effect on each others
    pharmacokinetics. No dose adjustments are needed
    when they are co-administered.

22
Vardenafil contd
  • Drug-Drug Interactions
  • Nifedipine
  • According to the product insert,
    co-administration of vardenafil 20mg and
    slow-release nifedipine 30mg or 60mg daily did
    not affect the Cmax or AUC of nifedipine.
    Nifedipine also did not change vardenafils
    plasma levels. Patients did experience an
    additional systolic/diastolic BP decrease of 6/5
    mmHg when on both medications.

23
Vardenafil contd
  • Drug-Drug Interactions
  • Ranitidine
  • According to the product insert, there is no
    pharmacokinetic interaction between these 2
    drugs.
  • S-warfarin
  • According to the package insert, no
    pharmacokinetic reactions occur between these two
    drugs. Vardenafil does not seem to have an effect
    on prothrombin time or other pharmacokinetic
    factors when taken with warfarin

24
Vardenafil
  • Drug-Drug Interactions
  • Digoxin
  • According to the product insert, there is no
    pharmacokinetic interaction between these two
    drugs.
  • Glyburide
  • According to the product insert, there is no
    pharmacokinetic interaction between these two
    drugs
  • Indinavir
  • According to the package insert, patients on
    indinavir (800mg TID) should not exceed 2.5mg of
    vardenafil per 24 hours. Indinavir increased
    vardenafils AUC by 16-fold, Cmax by 7-fold, and
    half-life by 2-fold.

25
Tadalafil
  • Drug-Class Interactions
  • H2-Antagonists
  • According to the package insert, there was no
    significant pharmacokinetic effect on tadalafil
    when stomach pH was increased
  • Drug-Drug Interactions
  • Alfuzosin
  • A randomized, double-blind, placebo-controlled,
    crossover study in 18 healthy normotensive adults
    studied the effects of tadalafil 20mg and
    alfuzosin 10mg daily. The mean standing and
    supine BP were slightly lower in those taking
    tadalafil compared to placebo, but these
    differences were not statistically significant

26
Tadalafil
  • Drug-Drug Interactions
  • Ritonavir (initially)
  • According to the PI, patients at steady state on
    ritonavir 500mg or 600mg twice per day had a 32
    increase in exposure (AUC) and a 30 decrease in
    Cmax when given a single dose of tadalafil
    compared to tadalafil 20mg alone. Patients on
    ritonavir 200mg BID experienced a 124 increase
    in AUC with no change in Cmax. Based on these
    results, its suggested that patients on potent
    3A4 inhibitors should take no more than 10mg of
    tadalafil per 72 hours.

27
Genelex Database
28
The Genelex Database
  • It lists the current drug interactions available
    in the literature.
  • Accounts for individual genotypes when
    metabolizing drugs.
  • Lists a severity rating.
  • Predicts interactions based on metabolism
    information when studies are not available.
  • It also lets users know when an interaction is
    based on literature and when it is based on the
    algorithm.

29
Accuracy of the Algorithm
30
When it was Right
  • There were instances where the algorithm was
    correct but it didnt predict the right
    percentage of change.

31
When it was Wrong
  • In many instances, the interaction I put in was a
    pharmacodynamic one so I wouldnt have expected
    the algorithm to get it since it focuses on
    pharmacokinetics. Although they were counted as
    part of the total Wrong, I dont think it was
    actually wrong. In actuality, the number of
    pharmacokinetic interactions that were Wrong
    was 7.

32
References
  • Hedaya MA, El-Afify DR, El-Maghraby GM. The
    effect of ciprofloxacin and clarithromycin on
    sildenafil oral bioavailability in human
    volunteers. Biopharm Drug Dispos 200627103-110.
  • Jetter A, Kinzig-Schippers M, Walchner-Bonjean M,
    et al. Effects of grapefruit juice on the
    pharmacokinetics of sildenafil. Clin Pharmacol
    Ther 20027121-29.
  • Kloner RA, Jackson G, Emmick JT, et al.
    Interactions between the phosphodiesterase 5
    inhibitor, talalafil and 2 a-blockers, doxazosin
    and tamsulosin in healthy normotensive men. J
    Urol 20041721935-1940.
  • Kloner RA. Pharmacology and drug interaction
    effects of the phosphodiesterase 5 inhibitors
    focus on a-blocker interactions. Am J Cardiol
    20059642-46.
  • Mehrotra N, Gupta M, Kovar A, et al. The role of
    pharmacokinetics and pharmacodynamics in
    phosphodiesterase-5 inhibitor therapy. Int J
    Impot Res 2007 19253-264.
  • Bank AJ, Kelly AS, Kaiser DR, et al. The effects
    of quinapril and atorvastatin on the
    responsiveness to sildenafil in men with erectile
    dysfunction. Vasc Med 200611251-257.
  • Nieminen T, tammela TL, Koobi T, et al. The
    effects of tamsulosin and sildenafil in separate
    and combined regimens on detailed hemodynamics in
    patients with benign prostatic enlargement. J
    Urol 20061762551-2556.
  • Ring BJ, Patterson BE, Mitchell MI, et al. Effect
    of tadalafil on cytochrome p450 3A4-mediated
    clearance studies in vitro and in vivo. Clin
    Pharmacol Ther 20057763-75.
  • Giuliano F, Kaplan SA, Cabanis M, et al.
    Hemodynamic interaction study between the
    alpha1-blocker alfuzosin and the
    phosphodiesterase-5 inhibitor tadalafil in
    middle-aged healthy male subjects. Urology
    2006671199-1204.
  • Therapeutics (Pharm 562) Class Lecture notes from
    5/23/2007
  • Product Insert Sildenafil
  • Product Insert Tadalafil
  • Product Insert Vardenafil
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