Does ENOXAPARIN Cause Suspected product quality issue? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Suspected product quality issue have been filed in association with ENOXAPARIN (Enoxaparin Sodium). This represents 0.0% of all adverse event reports for ENOXAPARIN.
6
Reports of Suspected product quality issue with ENOXAPARIN
0.0%
of all ENOXAPARIN reports
0
Deaths
1
Hospitalizations
How Dangerous Is Suspected product quality issue From ENOXAPARIN?
Of the 6 reports, 1 (16.7%) required hospitalization, and 2 (33.3%) were considered life-threatening.
Is Suspected product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ENOXAPARIN. However, 6 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 Suspected product quality issue?
AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE (64)
LEVOTHYROXINE (37)
HUMAN IMMUNOGLOBULIN G (32)
ESTRADIOL (30)
ONABOTULINUMTOXINA (30)
SODIUM (30)
CLONAZEPAM (29)
AFLIBERCEPT (27)
INSULIN GLARGINE (27)
IOPROMIDE (25)
Which ENOXAPARIN Alternatives Have Lower Suspected product quality issue Risk?
ENOXAPARIN vs ENOXAPARIN - WINTHROP
ENOXAPARIN vs ENSIFENTRINE
ENOXAPARIN vs ENTACAPONE
ENOXAPARIN vs ENTECAVIR
ENOXAPARIN vs ENTINOSTAT