Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Tedizolid phosphate
Drug ID BADD_D02136
Description Drug-resistant bacteria, such as methicillin-resistant _Staphylococcus aureus_, vancomycin-resistant _Enterococcus faecium_, and penicillin-resistant _Streptococcus penumoniae_, represent a massive public health threat.[A199086, A199131] Tedizolid is a member of the oxazolidinone class of antibiotics, which includes the previously approved [linezolid] and is generally effective against multidrug-resistant Gram-positive bacteria. Tedizolid is indicated for the treatment of acute bacterial skin and skin structure infections (ABSSSI) and is generally more effective and more tolerable than [linezolid].[L11232, A199086, A199050] Tedizolid was approved by the FDA on June 20, 2014, for sale by Cubist Pharmaceuticals as tedizolid phosphate (SIVEXTRO®). This product is currently available as both an oral tablet and as a powder for intravenous injection.[L11232]
Indications and Usage Tedizolid is indicated for the treatment of acute bacterial infections of the skin and skin structure (ABSSSI). To prevent drug resistance, tedizolid should only be used for infections that are caused by susceptible bacteria.[L11232]
Marketing Status approved
ATC Code Not Available
DrugBank ID DB09042
KEGG ID D09686
MeSH ID C515040
PubChem ID 11476460
TTD Drug ID D0DI6L
NDC Product Code 72000-310; 72000-320; 66406-0206; 42765-022; 67919-040; 67919-041; 68225-066; 65392-2912
UNII O7DRJ6R4DW
Synonyms tedizolid phosphate | torezolid phosphate | TR 701 | TR-701 | DA 7218 | DA7218 | DA-7218 | Sivextro
Chemical Information
Molecular Formula C17H16FN6O6P
CAS Registry Number 856867-55-5
SMILES CN1N=C(N=N1)C2=NC=C(C=C2)C3=C(C=C(C=C3)N4CC(OC4=O)COP(=O)(O)O)F
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice.
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Visual impairment06.02.10.013---
Vitreous floaters06.09.01.005--
Vomiting07.01.07.003--
White blood cell count decreased13.01.06.012--
Infusion related reaction08.01.03.002; 10.01.01.017; 12.02.05.009--
Transaminases increased13.03.04.036---
Adverse event08.06.01.010--
Optic nerve disorder06.02.08.001; 17.04.05.004--
Renal impairment20.01.03.010--
Vulvovaginal mycotic infection11.03.05.004; 21.14.02.004---
Multiple organ dysfunction syndrome08.01.03.057-
Drug effective for unapproved indication08.06.01.037; 12.09.02.001--
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