PARAGARD 380A Adverse Event: Device dislocation

Name: PARAGARD 380A Adverse Event: Device dislocation
Creator: FDATracker

PARAGARD 380A Adverse Event: Device dislocation is one of 4,500 adverse events in the FDATracker dataset. Key details — Primary drug: PARAGARD 380A; Product category: Drug; Primary reaction: Device dislocation.

Primary drug	PARAGARD 380A
Product category	Drug
Primary reaction	Device dislocation
All reactions	Device dislocation; Pelvic pain
Seriousness	Serious
Patient outcome	Recovered/Resolved
Patient sex	Female
All drugs reported	PARAGARD 380A
Reporter country	US
Reporter type	3
Report date	20140312
Report ID	10004481

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