Does PARAGARD 380A Cause Device breakage? 160 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 160 reports of Device breakage have been filed in association with PARAGARD 380A. This represents 8.9% of all adverse event reports for PARAGARD 380A.
160
Reports of Device breakage with PARAGARD 380A
8.9%
of all PARAGARD 380A reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device breakage From PARAGARD 380A?
Of the 160 reports.
Is Device breakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PARAGARD 380A. However, 160 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)
Menorrhagia (128)
Metrorrhagia (115)
Embedded device (107)
Pain (107)
Medical device complication (91)
Muscle spasms (89)
What Other Drugs Cause Device breakage?
COPPER (9,201)
SOMATROPIN (7,761)
ETONOGESTREL (4,140)
LEVONORGESTREL (2,726)
ETHINYL ESTRADIOL\ETONOGESTREL (741)
CARBIDOPA\LEVODOPA (634)
TREPROSTINIL (396)
ADALIMUMAB (375)
ALBUTEROL (256)
EPOPROSTENOL (240)
Which PARAGARD 380A Alternatives Have Lower Device breakage Risk?
PARAGARD 380A vs PERAMPANEL
PARAGARD 380A vs PERFLUTREN
PARAGARD 380A vs PHENOBARBITAL
PARAGARD 380A vs PHENYLEPHRINE
PARAGARD 380A vs PHENYLEPHRINE\PHENYLEPHRINE