Does LEVONORGESTREL Cause Product use issue? 339 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 339 reports of Product use issue have been filed in association with LEVONORGESTREL (Mirena). This represents 0.3% of all adverse event reports for LEVONORGESTREL.
339
Reports of Product use issue with LEVONORGESTREL
0.3%
of all LEVONORGESTREL reports
1
Deaths
29
Hospitalizations
How Dangerous Is Product use issue From LEVONORGESTREL?
Of the 339 reports, 1 (0.3%) resulted in death, 29 (8.6%) required hospitalization, and 1 (0.3%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEVONORGESTREL. However, 339 reports have been filed with the FAERS database.
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 Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which LEVONORGESTREL Alternatives Have Lower Product use issue Risk?
LEVONORGESTREL vs LEVORPHANOL
LEVONORGESTREL vs LEVOSIMENDAN
LEVONORGESTREL vs LEVOSULPIRIDE
LEVONORGESTREL vs LEVOTHYROXINE
LEVONORGESTREL vs LEVOTHYROXINE\LEVOTHYROXINE