Does AXITINIB Cause Wrong technique in product usage process? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Wrong technique in product usage process have been filed in association with AXITINIB (INLYTA). This represents 0.1% of all adverse event reports for AXITINIB.
16
Reports of Wrong technique in product usage process with AXITINIB
0.1%
of all AXITINIB reports
2
Deaths
1
Hospitalizations
How Dangerous Is Wrong technique in product usage process From AXITINIB?
Of the 16 reports, 2 (12.5%) resulted in death, 1 (6.3%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AXITINIB. However, 16 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which AXITINIB Alternatives Have Lower Wrong technique in product usage process Risk?
AXITINIB vs AZACITIDINE
AXITINIB vs AZATHIOPRINE
AXITINIB vs AZD-1222
AXITINIB vs AZELAIC ACID
AXITINIB vs AZELASTINE