Does RIPRETINIB Cause Post procedural complication? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Post procedural complication have been filed in association with RIPRETINIB (QINLOCK). This represents 0.1% of all adverse event reports for RIPRETINIB.
5
Reports of Post procedural complication with RIPRETINIB
0.1%
of all RIPRETINIB reports
0
Deaths
4
Hospitalizations
How Dangerous Is Post procedural complication From RIPRETINIB?
Of the 5 reports, 4 (80.0%) required hospitalization.
Is Post procedural complication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RIPRETINIB. However, 5 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 Post procedural complication?
ADALIMUMAB (2,494)
ETANERCEPT (318)
CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (244)
UPADACITINIB (241)
RISANKIZUMAB-RZAA (232)
INFLIXIMAB (217)
METHOTREXATE (188)
TREPROSTINIL (174)
HUMAN IMMUNOGLOBULIN G (159)
PREDNISONE (157)
Which RIPRETINIB Alternatives Have Lower Post procedural complication Risk?
RIPRETINIB vs RISANKIZUMAB
RIPRETINIB vs RISANKIZUMAB-RZAA
RIPRETINIB vs RISDIPLAM
RIPRETINIB vs RISEDRONATE
RIPRETINIB vs RISEDRONIC ACID