Does PARAGARD 380A Cause Device dislocation? 479 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 479 reports of Device dislocation have been filed in association with PARAGARD 380A. This represents 26.6% of all adverse event reports for PARAGARD 380A.
479
Reports of Device dislocation with PARAGARD 380A
26.6%
of all PARAGARD 380A reports
0
Deaths
2
Hospitalizations
How Dangerous Is Device dislocation From PARAGARD 380A?
Of the 479 reports, 2 (0.4%) required hospitalization.
Is Device dislocation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PARAGARD 380A. However, 479 reports have been filed with the FAERS database.
What Other Side Effects Does PARAGARD 380A Cause?
Device expulsion (685)
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 dislocation?
LEVONORGESTREL (13,757)
COPPER (6,955)
CARBIDOPA\LEVODOPA (2,937)
ETONOGESTREL (2,909)
TREPROSTINIL (1,626)
MIRENA (677)
BACLOFEN (492)
ADALIMUMAB (372)
EPOPROSTENOL (358)
DEXAMETHASONE (290)
Which PARAGARD 380A Alternatives Have Lower Device dislocation Risk?
PARAGARD 380A vs PERAMPANEL
PARAGARD 380A vs PERFLUTREN
PARAGARD 380A vs PHENOBARBITAL
PARAGARD 380A vs PHENYLEPHRINE
PARAGARD 380A vs PHENYLEPHRINE\PHENYLEPHRINE