Does LINEZOLID Cause Incorrect product administration duration? 87 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 87 reports of Incorrect product administration duration have been filed in association with LINEZOLID (Linezolid). This represents 0.5% of all adverse event reports for LINEZOLID.
87
Reports of Incorrect product administration duration with LINEZOLID
0.5%
of all LINEZOLID reports
25
Deaths
38
Hospitalizations
How Dangerous Is Incorrect product administration duration From LINEZOLID?
Of the 87 reports, 25 (28.7%) resulted in death, 38 (43.7%) required hospitalization, and 5 (5.7%) 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 LINEZOLID. However, 87 reports have been filed with the FAERS database.
What Other Side Effects Does LINEZOLID Cause?
Off label use (1,781)
Thrombocytopenia (1,588)
Drug ineffective (1,303)
Anaemia (1,294)
Lactic acidosis (824)
Nausea (800)
Neuropathy peripheral (748)
Vomiting (716)
Drug interaction (658)
Pancytopenia (638)
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 LINEZOLID Alternatives Have Lower Incorrect product administration duration Risk?
LINEZOLID vs LINZESS
LINEZOLID vs LIORESAL
LINEZOLID vs LIORESAL INTRATHECAL
LINEZOLID vs LIORESAL INTRATHECAL /ML
LINEZOLID vs LIOTHYRONINE