This form is not for reporting adverse events or product complaints. To report one, see Reporting Adverse Events and Product Complaints below.
 

By providing the information above and clicking “Submit,” you agree to permit Liquidia and others working on behalf of Liquidia to use this information to provide you with information, services, communications, and/or marketing materials about our product, studies and disease-related materials, and to use this information for market research purposes, and otherwise, all as described in our Privacy Policy. At any time, you can be removed from the contact list for YUTREPIA by contacting privacy@liquidia.com or as described in our Privacy Policy.

Reporting Adverse Events and Product Complaints

What is an adverse event?
Any untoward medical occurrence in a patient administered a product, which does not necessarily have a causal relationship with the treatment. An adverse event (AE) can be any unfavorable and unintended sign (for example, an abnormal laboratory finding), symptom, or disease temporally associated with the use of a product, whether or not it is considered related to the product. 

 

Why report side effects?
By reporting side effects for Liquidia products, you help us to ensure the safety of our products and our patients. Your information will also enable Liquidia to fulfill its reporting responsibilities to health authorities, which requires that we provide information on side effects with our products - even in cases where a relationship between the product and the effect is not established.
 

 

To report an adverse event or product complaint for YUTREPIA®

 

 

To report an adverse event or product complaint for Treprostinil injection

 


 

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