Does TEDIZOLID Cause Product dose omission issue? 29 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 29 reports of Product dose omission issue have been filed in association with TEDIZOLID (SIVEXTRO). This represents 3.8% of all adverse event reports for TEDIZOLID.
29
Reports of Product dose omission issue with TEDIZOLID
3.8%
of all TEDIZOLID reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product dose omission issue From TEDIZOLID?
Of the 29 reports, 3 (10.3%) required hospitalization, and 1 (3.4%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TEDIZOLID. However, 29 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 Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which TEDIZOLID Alternatives Have Lower Product dose omission issue Risk?
TEDIZOLID vs TEDUGLUTIDE
TEDIZOLID vs TEDUGLUTIDE\WATER
TEDIZOLID vs TEGAFUR
TEDIZOLID vs TEGAFUR\URACIL
TEDIZOLID vs TEGASEROD