Does RIPRETINIB Cause Product administration interrupted? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Product administration interrupted have been filed in association with RIPRETINIB (QINLOCK). This represents 0.3% of all adverse event reports for RIPRETINIB.
13
Reports of Product administration interrupted with RIPRETINIB
0.3%
of all RIPRETINIB reports
1
Deaths
2
Hospitalizations
How Dangerous Is Product administration interrupted From RIPRETINIB?
Of the 13 reports, 1 (7.7%) resulted in death, 2 (15.4%) required hospitalization.
Is Product administration interrupted Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RIPRETINIB. However, 13 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 Product administration interrupted?
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (1,446)
SODIUM OXYBATE (1,272)
CANNABIDIOL (511)
ISOTRETINOIN (503)
APREMILAST (314)
TREPROSTINIL (295)
EPOPROSTENOL (205)
LENALIDOMIDE (146)
ETANERCEPT (142)
INTERFERON BETA-1A (115)
Which RIPRETINIB Alternatives Have Lower Product administration interrupted Risk?
RIPRETINIB vs RISANKIZUMAB
RIPRETINIB vs RISANKIZUMAB-RZAA
RIPRETINIB vs RISDIPLAM
RIPRETINIB vs RISEDRONATE
RIPRETINIB vs RISEDRONIC ACID