Does RIPRETINIB Cause Product solubility abnormal? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Product solubility abnormal have been filed in association with RIPRETINIB (QINLOCK). This represents 0.2% of all adverse event reports for RIPRETINIB.
8
Reports of Product solubility abnormal with RIPRETINIB
0.2%
of all RIPRETINIB reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product solubility abnormal From RIPRETINIB?
Of the 8 reports, 2 (25.0%) required hospitalization.
Is Product solubility abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RIPRETINIB. However, 8 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 solubility abnormal?
BUPRENORPHINE (498)
BUPRENORPHINE\NALOXONE (274)
POLYETHYLENE GLYCOL 3350 (220)
CHOLESTYRAMINE (193)
PATIROMER (107)
LEVOTHYROXINE (100)
SOMATROPIN (98)
EXENATIDE (97)
ESTRADIOL (94)
NITROGLYCERIN (81)
Which RIPRETINIB Alternatives Have Lower Product solubility abnormal Risk?
RIPRETINIB vs RISANKIZUMAB
RIPRETINIB vs RISANKIZUMAB-RZAA
RIPRETINIB vs RISDIPLAM
RIPRETINIB vs RISEDRONATE
RIPRETINIB vs RISEDRONIC ACID