Does PARAGARD 380A Cause Embedded device? 107 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 107 reports of Embedded device have been filed in association with PARAGARD 380A. This represents 5.9% of all adverse event reports for PARAGARD 380A.
107
Reports of Embedded device with PARAGARD 380A
5.9%
of all PARAGARD 380A reports
0
Deaths
2
Hospitalizations
How Dangerous Is Embedded device From PARAGARD 380A?
Of the 107 reports, 2 (1.9%) required hospitalization.
Is Embedded device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PARAGARD 380A. However, 107 reports have been filed with the FAERS database.
What Other Side Effects Does PARAGARD 380A Cause?
Device expulsion (685)
Device dislocation (479)
Vaginal haemorrhage (186)
Pelvic pain (177)
Device breakage (160)
Menorrhagia (128)
Metrorrhagia (115)
Pain (107)
Medical device complication (91)
Muscle spasms (89)
What Other Drugs Cause Embedded device?
COPPER (3,425)
LEVONORGESTREL (3,413)
CARBIDOPA\LEVODOPA (736)
MIRENA (159)
ETONOGESTREL (30)
UNSPECIFIED INGREDIENT (12)
ADALIMUMAB (11)
TREPROSTINIL (8)
Which PARAGARD 380A Alternatives Have Lower Embedded device Risk?
PARAGARD 380A vs PERAMPANEL
PARAGARD 380A vs PERFLUTREN
PARAGARD 380A vs PHENOBARBITAL
PARAGARD 380A vs PHENYLEPHRINE
PARAGARD 380A vs PHENYLEPHRINE\PHENYLEPHRINE