Does RIPRETINIB Cause Adverse event? 214 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 214 reports of Adverse event have been filed in association with RIPRETINIB (QINLOCK). This represents 4.8% of all adverse event reports for RIPRETINIB.
214
Reports of Adverse event with RIPRETINIB
4.8%
of all RIPRETINIB reports
5
Deaths
36
Hospitalizations
How Dangerous Is Adverse event From RIPRETINIB?
Of the 214 reports, 5 (2.3%) resulted in death, 36 (16.8%) required hospitalization, and 2 (0.9%) were considered life-threatening.
Is Adverse event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RIPRETINIB. However, 214 reports have been filed with the FAERS database.
What Other Side Effects Does RIPRETINIB Cause?
Fatigue (582)
Alopecia (517)
Extra dose administered (357)
Death (356)
Underdose (345)
Nausea (292)
Drug ineffective (291)
Disease progression (290)
Hospitalisation (280)
Neoplasm progression (263)
What Other Drugs Cause Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which RIPRETINIB Alternatives Have Lower Adverse event Risk?
RIPRETINIB vs RISANKIZUMAB
RIPRETINIB vs RISANKIZUMAB-RZAA
RIPRETINIB vs RISDIPLAM
RIPRETINIB vs RISEDRONATE
RIPRETINIB vs RISEDRONIC ACID