Information about Iloprost
Iloprost, an inhalation solution, is sold under the name Ventavis® and is used to treat pulmonary arterial hypertension (PAH). It was developed by the pharmaceutical company Schering AG and is marketed by Schering AG in Europe and Actelion Pharmaceuticals in the USA.
The approved dosing regimen for iloprost is 6 to 9 times daily (no more than every 2 hours) during waking hours, according to individual need and tolerability. The significant clinical effects observed in the pivotal study of patients with PAH were achieved with a median dose of 30 mcg per day (range: 12.5 to 45 mcg delivered at the mouthpiece), corresponding to 6 daily inhalations of 5 mcg. The majority of patients (> 80%) in the pivotal study used this median dose or a higher dose with an excellent treatment compliance after 12 weeks.
The first inhaled dose of iloprost should be 2.5 mcg (as delivered at the mouthpiece). If this dose is well tolerated, dosing should be increased to 5 mcg and maintained at that dose. Any patient who cannot tolerate the 5 mcg dose should be maintained at 2.5 mcg.
Each inhalation treatment requires one entire single-use ampule. Each single-use ampule delivers a concentration of 10 mcg/mL to the medication chamber of either the I-Neb® AAD® or Prodose® AAD® System, and delivers a nominal dose of either 2.5 mcg or 5.0 mcg to the mouthpiece. After each inhalation session, any solution remaining in the medication chamber should be discarded. Use of the remaining solution, even if the reservoir is “topped off” with fresh medication, will result in unpredictable dosing. Patients should follow the manufacturer’s instructions for cleaning the I-Neb® AAD® or Prodose® AAD® System components after each dose administration.
Complete information regarding use of iloprost in specific populations (e.g. nursing mothers, pediatrics, patients with hepatic or renal impairment), drug interactions, and overdosage can be found in full prescribing information.
Warnings:
Clinical pharmacology
Iloprost is a synthetic analogue of prostacyclin PGI2. Iloprost dilates systemic and pulmonary arterial vascular beds. It also affects platelet aggregation but the relevance of this effect to the treatment of pulmonary hypertension is unknown. The two diastereoisomers of iloprost differ in their potency in dilating blood vessels, with the 4S isomer substantially more potent than the 4R isomer.Dosage and administration
In the U.S., iloprost is intended to be inhaled specifically using the I-Neb® AAD® or Prodose® AAD® delivery systems. Iloprost has not been approved for use with other brands of nebulizers.The approved dosing regimen for iloprost is 6 to 9 times daily (no more than every 2 hours) during waking hours, according to individual need and tolerability. The significant clinical effects observed in the pivotal study of patients with PAH were achieved with a median dose of 30 mcg per day (range: 12.5 to 45 mcg delivered at the mouthpiece), corresponding to 6 daily inhalations of 5 mcg. The majority of patients (> 80%) in the pivotal study used this median dose or a higher dose with an excellent treatment compliance after 12 weeks.
The first inhaled dose of iloprost should be 2.5 mcg (as delivered at the mouthpiece). If this dose is well tolerated, dosing should be increased to 5 mcg and maintained at that dose. Any patient who cannot tolerate the 5 mcg dose should be maintained at 2.5 mcg.
Each inhalation treatment requires one entire single-use ampule. Each single-use ampule delivers a concentration of 10 mcg/mL to the medication chamber of either the I-Neb® AAD® or Prodose® AAD® System, and delivers a nominal dose of either 2.5 mcg or 5.0 mcg to the mouthpiece. After each inhalation session, any solution remaining in the medication chamber should be discarded. Use of the remaining solution, even if the reservoir is “topped off” with fresh medication, will result in unpredictable dosing. Patients should follow the manufacturer’s instructions for cleaning the I-Neb® AAD® or Prodose® AAD® System components after each dose administration.
Complete information regarding use of iloprost in specific populations (e.g. nursing mothers, pediatrics, patients with hepatic or renal impairment), drug interactions, and overdosage can be found in full prescribing information.
Important safety information
Contraindications:- There are no known contraindications.
- In clinical studies, common adverse reactions due to inhaled iloprost included: vasodilation (flushing, 27%), cough (39%), headache (30%), flu syndrome (14%), nausea (13%), neck spasms (12%), hypotension (11%), insomnia (8%), and fainting (syncope) (8%); other serious adverse events reported with the use of Ventavis included congestive heart failure, chest pain, supraventricular tachycardia, dyspnea, swelling of the limbs (especially around the ankles and feet), and kidney failure.
Warnings:
- Iloprost as Ventavis is intended for inhalation administration only via the I-Neb® AAD® or Prodose® AAD® Systems, pulmonary drug delivery devices. It has not been studied with any other nebulizers.
- Vital signs should be monitored while initiating inhaled iloprost therapy. Dose adjustments or a change in therapy should be considered if exertional syncope occurs. Inhaled Iloprost should not be initiated in patients with systolic blood pressure lower than 85 mm Hg. Iloprost should be stopped immediately if signs of pulmonary edema occur. This may be a sign of pulmonary venous hypertension. Iloprost has not been evaluated in patients with chronic obstructive pulmonary disease (COPD), severe asthma, or with acute pulmonary infections.
- Should signs of pulmonary edema occur when inhaled iloprost is administered in patients with pulmonary hypertension, the treatment should be stopped immediately. This may be a sign of pulmonary venous hypertension.
See also
References
- Ventavis Package insert prescribing information available in PDF format.
- H. Olschewski et al, Inhaled Iloprost for Severe Pulmonary Hypertension., NEJM, Volume 347:322-329, August 1, 2002, Number 5 http://content.nejm.org/cgi/content/abstract/347/5/322
- ATS 2005. The International Conference of the American Thoracic Society. 20 May - 25 May 2005. San Diego, CA.
External links
- Home page for Ventavis in the U.S.
- Home page for Ventavis in the EU
- Cotherix, Inc. (Company website) - marketer of Ventavis; prescribing information available in PDF format.
- FDA Web Site for Ventavis Consumer Information
Medications used in the management of pulmonary arterial hypertension (B01, C02) | |
|---|---|
| Prostacyclin analogues | Beraprost, Epoprostenol, Iloprost, Treprostinil |
| Endothelin receptor antagonists | Ambrisentan, Bosentan, Sitaxsentan |
| PDE5 inhibitors | Sildenafil, Tadalafil |
| Adjunctive therapy | Calcium channel blockers, Diuretics, Digoxin, Oxygen therapy, Warfarin |
Eicosanoids: prostaglandins | |
|---|---|
| Endogenous/series 2 | D2 - E2 (Dinoprostone) - H2 - I2 (Prostacyclin) |
| Prostaglandin analogues | Alprostadil - Beraprost - Bimatoprost - Carboprost - Enprostil - Iloprost - Latanoprost - Misoprostol - Travoprost - Treprostinil |
MeSH D006976 In medicine, pulmonary hypertension (PH) is an increase in blood pressure in the pulmonary artery or lung vasculature, leading to shortness of breath, dizziness, fainting, and other symptoms, all of which are exacerbated by exertion.
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A pharmaceutical company, or drug company, is a commercial business whose focus is to research, develop, market and/or distribute drugs, most commonly in the context of healthcare. They can deal in generic and/or brand medications.
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Schering AG was a research-centered pharmaceutical company founded in 1851 that merged with Bayer in December 2006. At that time the company employed more than 26,000 people in 140 subsidiaries all over the world. The company's headquarters are in Berlin-Wedding, Germany.
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Schering AG was a research-centered pharmaceutical company founded in 1851 that merged with Bayer in December 2006. At that time the company employed more than 26,000 people in 140 subsidiaries all over the world. The company's headquarters are in Berlin-Wedding, Germany.
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Prostacyclin is a member of the family of lipid molecules known as eicosanoids. Epoprostenol (brand name Flolan) is a synthetic form of prostacyclin, approved by the FDA as a medicine in 1995.
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The blood vessels are part of the cardiovascular system and function to transport blood throughout the body. The most important types, arteries and veins, carry blood away from or towards the heart, respectively.
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Platelets, or thrombocytes, are the cell fragments circulating in the blood that are involved in the cellular mechanisms of primary hemostasis leading to the formation of blood clots.
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In chemistry, isomers are molecules with the same chemical formula and often with the same kinds of chemical bonds between atoms, but in which the atoms are arranged differently (analogous to a chemical anagram).
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nebulizer is a device used to administer medication to people in forms of a liquid mist to the airways. It is commonly used in treating cystic fibrosis, asthma, and other respiratory diseases.
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A vasodilator is a drug or chemical that relaxes the smooth muscle in blood vessels, which causes them to dilate. Dilation of arterial blood vessels (mainly arterioles) lead to a decrease in blood pressure.
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Trismus (also known as lock jaw) is the inability to normally open the mouth due to inflammation of muscles of mastication. It is a frequent sequel to surgical removal of mandibular third molars (lower wisdom teeth).
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MeSH D007022
In physiology and medicine, hypotension refers to an abnormally low blood pressure. This is best understood as a physiologic state, rather than a disease. It is often associated with shock, though not necessarily indicative of it.
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In physiology and medicine, hypotension refers to an abnormally low blood pressure. This is best understood as a physiologic state, rather than a disease. It is often associated with shock, though not necessarily indicative of it.
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Fainting
Classifications and external resources
ICD-10 R 55.
ICD-9 780.2
DiseasesDB 27303
eMedicine med/3385 ped/2188 emerg/876
MeSH D013575 Fainting, also called syncope
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Classifications and external resources
ICD-10 R 55.
ICD-9 780.2
DiseasesDB 27303
eMedicine med/3385 ped/2188 emerg/876
MeSH D013575 Fainting, also called syncope
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Heart failure
Classification & external resources
ICD-10 I 50.0
ICD-9 428.0
DiseasesDB 16209
MedlinePlus 000158
eMedicine med/3552
MeSH D006333
Congestive heart failure (CHF), also called
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Classification & external resources
ICD-10 I 50.0
ICD-9 428.0
DiseasesDB 16209
MedlinePlus 000158
eMedicine med/3552
MeSH D006333
Congestive heart failure (CHF), also called
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Tachycardia
Classifications and external resources
ICD-10 R 00.0
ICD-9 785.0
MeSH D013610 Tachycardia is a form of cardiac arrhythmia which refers to a rapid beating of the heart.
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Classifications and external resources
ICD-10 R 00.0
ICD-9 785.0
MeSH D013610 Tachycardia is a form of cardiac arrhythmia which refers to a rapid beating of the heart.
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Dyspnea
Classifications and external resources
ICD-10 R 06.8
ICD-9 786.0
DiseasesDB 15892
MedlinePlus 003075 Dyspnea or Dyspnoea (Pronounced disp-nee-ah, from the Latin dyspnoea, Greek dyspnoia from
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Classifications and external resources
ICD-10 R 06.8
ICD-9 786.0
DiseasesDB 15892
MedlinePlus 003075 Dyspnea or Dyspnoea (Pronounced disp-nee-ah, from the Latin dyspnoea, Greek dyspnoia from
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Peripheral edema
Classifications and external resources
ICD-10 R 60.0
ICD-9 782.3
Peripheral edema is the swelling of tissues, usually in the lower limbs, due the accumulation of fluids.
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Classifications and external resources
ICD-10 R 60.0
ICD-9 782.3
Peripheral edema is the swelling of tissues, usually in the lower limbs, due the accumulation of fluids.
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MeSH C12.777.419.780.500 Renal failure or kidney failure is the condition in which the kidneys fail to function adequately.
Biochemically, it is typically detected by an elevated serum creatinine.
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Biochemically, it is typically detected by an elevated serum creatinine.
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Heart failure
Classification & external resources
ICD-10 I 50.0
ICD-9 428.0
DiseasesDB 16209
MedlinePlus 000158
eMedicine med/3552
MeSH D006333
Congestive heart failure (CHF), also called
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Classification & external resources
ICD-10 I 50.0
ICD-9 428.0
DiseasesDB 16209
MedlinePlus 000158
eMedicine med/3552
MeSH D006333
Congestive heart failure (CHF), also called
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MeSH D013617 A supraventricular tachycardia (SVT) is a tachycardia or rapid rhythm of the heart in which the origin of the electrical signal is either the atria or the AV node.
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Dyspnea
Classifications and external resources
ICD-10 R 06.8
ICD-9 786.0
DiseasesDB 15892
MedlinePlus 003075 Dyspnea or Dyspnoea (Pronounced disp-nee-ah, from the Latin dyspnoea, Greek dyspnoia from
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Classifications and external resources
ICD-10 R 06.8
ICD-9 786.0
DiseasesDB 15892
MedlinePlus 003075 Dyspnea or Dyspnoea (Pronounced disp-nee-ah, from the Latin dyspnoea, Greek dyspnoia from
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Peripheral edema
Classifications and external resources
ICD-10 R 60.0
ICD-9 782.3
Peripheral edema is the swelling of tissues, usually in the lower limbs, due the accumulation of fluids.
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Classifications and external resources
ICD-10 R 60.0
ICD-9 782.3
Peripheral edema is the swelling of tissues, usually in the lower limbs, due the accumulation of fluids.
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Chronic obstructive pulmonary disease
Classification & external resources
ICD-10 J 40. - J 44. , J 47.
ICD-9 490 - 496
OMIM 606963
DiseasesDB 2672
MedlinePlus 000091
eMedicine med/373 emerg/99
MeSH C08.381.495.
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Classification & external resources
ICD-10 J 40. - J 44. , J 47.
ICD-9 490 - 496
OMIM 606963
DiseasesDB 2672
MedlinePlus 000091
eMedicine med/373 emerg/99
MeSH C08.381.495.
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Asthma
Classification & external resources
ICD-10 J 45.
ICD-9 493
OMIM 600807
DiseasesDB 1006
MedlinePlus 000141
eMedicine med/177 emerg/43
MeSH C08.127.
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Classification & external resources
ICD-10 J 45.
ICD-9 493
OMIM 600807
DiseasesDB 1006
MedlinePlus 000141
eMedicine med/177 emerg/43
MeSH C08.127.
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MeSH D006976 In medicine, pulmonary hypertension (PH) is an increase in blood pressure in the pulmonary artery or lung vasculature, leading to shortness of breath, dizziness, fainting, and other symptoms, all of which are exacerbated by exertion.
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Thrombolytic drugs are used in medicine to dissolve blood clots in a procedure termed thrombolysis. They limit the damage caused by the blockage of the blood vessel.
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An anticoagulant is a substance that prevents coagulation; that is, it stops blood from clotting. A group of pharmaceuticals called anticoagulants can be used in vivo as a medication for thrombotic disorders.
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An antiplatelet drug is a member of a class of pharmaceuticals that decreases platelet aggregation and inhibits thrombus formation. They are effective in the arterial circulation, where anticoagulants have little effect.
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A section of the Anatomical Therapeutic Chemical Classification System.
B Blood and blood forming organs
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B Blood and blood forming organs
B01A Antithrombotic agents
B01AA Vitamin K antagonists
- B01AA01 Dicoumarol
- B01AA02 Phenindione
- B01AA03 Warfarin
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Vitamin K denotes a group of lipophilic, and hydrophobic, vitamins that are needed for the posttranslational modification of certain proteins, mostly required for blood coagulation. Chemically they are 2-methyl-1,4-naphthoquinone derivatives.
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