Does ENOXAPARIN Cause Incorrect product administration duration? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Incorrect product administration duration have been filed in association with ENOXAPARIN (Enoxaparin Sodium). This represents 0.0% of all adverse event reports for ENOXAPARIN.
8
Reports of Incorrect product administration duration with ENOXAPARIN
0.0%
of all ENOXAPARIN reports
0
Deaths
3
Hospitalizations
How Dangerous Is Incorrect product administration duration From ENOXAPARIN?
Of the 8 reports, 3 (37.5%) required hospitalization, and 1 (12.5%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ENOXAPARIN. However, 8 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which ENOXAPARIN Alternatives Have Lower Incorrect product administration duration Risk?
ENOXAPARIN vs ENOXAPARIN - WINTHROP
ENOXAPARIN vs ENSIFENTRINE
ENOXAPARIN vs ENTACAPONE
ENOXAPARIN vs ENTECAVIR
ENOXAPARIN vs ENTINOSTAT