LETAIRIS Adverse Event: Device dislocation

Name: LETAIRIS Adverse Event: Device dislocation
Creator: FDATracker

LETAIRIS Adverse Event: Device dislocation is one of 4,500 adverse events in the FDATracker dataset. Key details — Primary drug: LETAIRIS; Product category: Drug; Primary reaction: Device dislocation.

Primary drug	LETAIRIS
Product category	Drug
Primary reaction	Device dislocation
All reactions	Device dislocation
Seriousness	Not serious
Patient outcome	Unknown
Patient sex	Female
All drugs reported	LETAIRIS; REMODULIN; REVATIO
Reporter country	US
Reporter type	1
Report date	20140313
Report ID	10007076

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