Does LEVONORGESTREL Cause Embedded device? 3,413 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 3,413 reports of Embedded device have been filed in association with LEVONORGESTREL (Mirena). This represents 3.0% of all adverse event reports for LEVONORGESTREL.
3,413
Reports of Embedded device with LEVONORGESTREL
3.0%
of all LEVONORGESTREL reports
0
Deaths
507
Hospitalizations
How Dangerous Is Embedded device From LEVONORGESTREL?
Of the 3,413 reports, 507 (14.9%) required hospitalization, and 43 (1.3%) were considered life-threatening.
Is Embedded device Listed in the Official Label?
Yes, Embedded device is listed as a known adverse reaction in the official FDA drug label for LEVONORGESTREL.
What Other Side Effects Does LEVONORGESTREL Cause?
Device expulsion (27,572)
Device dislocation (13,757)
Vaginal haemorrhage (10,910)
Genital haemorrhage (7,968)
Drug ineffective (6,008)
Abdominal pain lower (5,938)
Procedural pain (5,572)
Uterine perforation (4,973)
Nausea (4,879)
Complication of device insertion (4,662)
What Other Drugs Cause Embedded device?
COPPER (3,425)
CARBIDOPA\LEVODOPA (736)
MIRENA (159)
PARAGARD 380A (107)
ETONOGESTREL (30)
UNSPECIFIED INGREDIENT (12)
ADALIMUMAB (11)
TREPROSTINIL (8)
Which LEVONORGESTREL Alternatives Have Lower Embedded device Risk?
LEVONORGESTREL vs LEVORPHANOL
LEVONORGESTREL vs LEVOSIMENDAN
LEVONORGESTREL vs LEVOSULPIRIDE
LEVONORGESTREL vs LEVOTHYROXINE
LEVONORGESTREL vs LEVOTHYROXINE\LEVOTHYROXINE