Does TEDIZOLID Cause Incorrect product administration duration? 17 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Incorrect product administration duration have been filed in association with TEDIZOLID (SIVEXTRO). This represents 2.2% of all adverse event reports for TEDIZOLID.
17
Reports of Incorrect product administration duration with TEDIZOLID
2.2%
of all TEDIZOLID reports
1
Deaths
5
Hospitalizations
How Dangerous Is Incorrect product administration duration From TEDIZOLID?
Of the 17 reports, 1 (5.9%) resulted in death, 5 (29.4%) required hospitalization, and 1 (5.9%) 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 TEDIZOLID. However, 17 reports have been filed with the FAERS database.
What Other Side Effects Does TEDIZOLID Cause?
Off label use (109)
Product use in unapproved indication (93)
Thrombocytopenia (75)
Drug ineffective (73)
Nausea (48)
Pancytopenia (44)
Anaemia (43)
No adverse event (37)
Product availability issue (33)
Neuropathy peripheral (32)
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 TEDIZOLID Alternatives Have Lower Incorrect product administration duration Risk?
TEDIZOLID vs TEDUGLUTIDE
TEDIZOLID vs TEDUGLUTIDE\WATER
TEDIZOLID vs TEGAFUR
TEDIZOLID vs TEGAFUR\URACIL
TEDIZOLID vs TEGASEROD