Does ENOXAPARIN Cause Intentional product use issue? 57 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 57 reports of Intentional product use issue have been filed in association with ENOXAPARIN (Enoxaparin Sodium). This represents 0.2% of all adverse event reports for ENOXAPARIN.
57
Reports of Intentional product use issue with ENOXAPARIN
0.2%
of all ENOXAPARIN reports
31
Deaths
16
Hospitalizations
How Dangerous Is Intentional product use issue From ENOXAPARIN?
Of the 57 reports, 31 (54.4%) resulted in death, 16 (28.1%) required hospitalization, and 10 (17.5%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ENOXAPARIN. However, 57 reports have been filed with the FAERS database.
What Other Side Effects Does ENOXAPARIN Cause?
Off label use (1,707)
Exposure during pregnancy (1,215)
Haemorrhage (1,059)
Foetal exposure during pregnancy (918)
Anaemia (914)
Thrombocytopenia (834)
Dyspnoea (822)
Maternal exposure during pregnancy (818)
Drug ineffective (769)
Nausea (708)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which ENOXAPARIN Alternatives Have Lower Intentional product use issue Risk?
ENOXAPARIN vs ENOXAPARIN - WINTHROP
ENOXAPARIN vs ENSIFENTRINE
ENOXAPARIN vs ENTACAPONE
ENOXAPARIN vs ENTECAVIR
ENOXAPARIN vs ENTINOSTAT