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Iloprost (Ventavis®) - PHA Online University

Iloprost (Ventavis®) - PHA Online University

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Actelion PAH Pathways ® (866-288-3546) offers a variety of options to cover either partial or full drugcosts for any patient with qualifying financial circumstances. Caring Voice Coalition (888-267-1440),an organization that provides grants to assist with drug cost for patients with chronic illnesses, mayalso provide coverage if the patient qualifies for such assistance.What are the frequent side effects of iloprost?The most common side effects include flushing (vasodilation), increased cough, headache, spasm ofjaw muscles that makes it difficult to open your mouth and may cause jaw discomfort (trismus),insomnia, nausea, low blood pressure, vomiting, increased alkaline phosphatase or GGT (liverenzymes measured in the blood), flu syndrome –like symptoms, back pain, tongue pain, fast orirregular heart rate or rhythm (palpitations), passing out (syncope), muscle cramps, coughing upblood (hemoptysis), and pneumonia.Hypotension leading to syncope has been observed; iloprost should therefore not be initiated inpatients with systolic blood pressure less than 85 mmHg.Pulmonary venous hypertension and pulmonary edema can occur in which case iloprost should bepromptly discontinued.<strong>Iloprost</strong> inhalation can induce narrowed breathing tubes (airways), called bronchospasm, manifest ascough, wheezing or shortness of breath.<strong>Iloprost</strong> solution can also irritate the eyes and skin. If iloprost comes in contact with the skin or eyes,rinse immediately with water.How are side effects of iloprost monitored?Vital signs should be monitored while initiating iloprost. <strong>Iloprost</strong> should generally be avoided if thesystemic systolic blood pressure is below 85 mmHg.If you experience any of the symptoms mentioned in the previous section, you should promptly notifyyour physician.What are considerations for use of iloprost in special populations?<strong>Iloprost</strong> has been shown to cause damage to the fetus (i.e. teratogenic) in rats. <strong>Iloprost</strong> has not beenevaluated in pregnant women or women who are breastfeeding. <strong>Iloprost</strong> should be used in pregnant ornursing mothers only if the potential benefit justifies the risk to the fetus or infant.Safety and efficacy in pediatric patients has not been established.Clinical studies did not include a sufficient number of patients over age 65 to determine either safetyor efficacy.<strong>Iloprost</strong> has not been evaluated in patients with impaired liver (hepatic) function; however,consideration should be given to increasing the dosing interval (e.g. 3 to 4 hours between doses) inpatients with moderate to severe hepatic impairment.<strong>Iloprost</strong> has not been evaluated in patients with impaired kidney (renal) function. Likewise, the effectof dialysis in unknown.Could a patient be allergic to iloprost?This is unlikely. An ampule of iloprost does not contain preservatives or sulfites. However, anymedication can cause side effects or sensitivities and patients should check with their doctor if theyexperience a problem.801 Roeder Rd, Ste. 1000 • Silver Spring, MD 20910 • (301) 565-3004 • www.<strong>PHA</strong>ssociation.org • www.<strong>PHA</strong><strong>Online</strong>Univ.org

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