Does PARAGARD 380A Cause Device expulsion? 685 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 685 reports of Device expulsion have been filed in association with PARAGARD 380A. This represents 38.0% of all adverse event reports for PARAGARD 380A.
685
Reports of Device expulsion with PARAGARD 380A
38.0%
of all PARAGARD 380A reports
0
Deaths
1
Hospitalizations
How Dangerous Is Device expulsion From PARAGARD 380A?
Of the 685 reports, 1 (0.1%) required hospitalization.
Is Device expulsion Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PARAGARD 380A. However, 685 reports have been filed with the FAERS database.
What Other Side Effects Does PARAGARD 380A Cause?
Device dislocation (479)
Vaginal haemorrhage (186)
Pelvic pain (177)
Device breakage (160)
Menorrhagia (128)
Metrorrhagia (115)
Embedded device (107)
Pain (107)
Medical device complication (91)
Muscle spasms (89)
What Other Drugs Cause Device expulsion?
LEVONORGESTREL (27,572)
COPPER (11,141)
ETONOGESTREL (1,993)
MIRENA (1,300)
ETHINYL ESTRADIOL\ETONOGESTREL (986)
CARBIDOPA\LEVODOPA (129)
NEXPLANON (98)
NUVARING (92)
ESTRADIOL (57)
HISTRELIN (22)
Which PARAGARD 380A Alternatives Have Lower Device expulsion Risk?
PARAGARD 380A vs PERAMPANEL
PARAGARD 380A vs PERFLUTREN
PARAGARD 380A vs PHENOBARBITAL
PARAGARD 380A vs PHENYLEPHRINE
PARAGARD 380A vs PHENYLEPHRINE\PHENYLEPHRINE