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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does RIPRETINIB Cause Product packaging quantity issue? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product packaging quantity issue have been filed in association with RIPRETINIB (QINLOCK). This represents 0.1% of all adverse event reports for RIPRETINIB.

5
Reports of Product packaging quantity issue with RIPRETINIB
0.1%
of all RIPRETINIB reports
0
Deaths
2
Hospitalizations

How Dangerous Is Product packaging quantity issue From RIPRETINIB?

Of the 5 reports, 2 (40.0%) required hospitalization, and 1 (20.0%) were considered life-threatening.

Is Product packaging quantity issue 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 Product packaging quantity issue?

LEUPROLIDE (523) ALBUTEROL (431) BUDESONIDE\FORMOTEROL (301) FENTANYL (286) BUPRENORPHINE (225) CYCLOSPORINE (206) ESTRADIOL (201) BIMATOPROST (177) RIVAROXABAN (174) EXENATIDE (154)

Which RIPRETINIB Alternatives Have Lower Product packaging quantity issue Risk?

RIPRETINIB vs RISANKIZUMAB RIPRETINIB vs RISANKIZUMAB-RZAA RIPRETINIB vs RISDIPLAM RIPRETINIB vs RISEDRONATE RIPRETINIB vs RISEDRONIC ACID

Related Pages

RIPRETINIB Full Profile All Product packaging quantity issue Reports All Drugs Causing Product packaging quantity issue RIPRETINIB Demographics