Does AXITINIB Cause Intentional dose omission? 27 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 27 reports of Intentional dose omission have been filed in association with AXITINIB (INLYTA). This represents 0.2% of all adverse event reports for AXITINIB.
27
Reports of Intentional dose omission with AXITINIB
0.2%
of all AXITINIB reports
1
Deaths
9
Hospitalizations
How Dangerous Is Intentional dose omission From AXITINIB?
Of the 27 reports, 1 (3.7%) resulted in death, 9 (33.3%) required hospitalization, and 1 (3.7%) were considered life-threatening.
Is Intentional dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AXITINIB. However, 27 reports have been filed with the FAERS database.
What Other Side Effects Does AXITINIB Cause?
Death (2,222)
Diarrhoea (2,187)
Fatigue (1,816)
Neoplasm progression (1,315)
Hypertension (1,146)
Off label use (1,075)
Nausea (955)
Decreased appetite (920)
Dysphonia (871)
Disease progression (768)
What Other Drugs Cause Intentional dose omission?
DUPILUMAB (2,269)
CERTOLIZUMAB PEGOL (1,253)
ADALIMUMAB (845)
TOFACITINIB (845)
INFLIXIMAB (815)
ABALOPARATIDE (623)
ETANERCEPT (615)
AMBRISENTAN (595)
SODIUM OXYBATE (580)
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)
Which AXITINIB Alternatives Have Lower Intentional dose omission Risk?
AXITINIB vs AZACITIDINE
AXITINIB vs AZATHIOPRINE
AXITINIB vs AZD-1222
AXITINIB vs AZELAIC ACID
AXITINIB vs AZELASTINE