Does REPOTRECTINIB Cause Treatment noncompliance? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Treatment noncompliance have been filed in association with REPOTRECTINIB (Augtyro). This represents 3.7% of all adverse event reports for REPOTRECTINIB.
7
Reports of Treatment noncompliance with REPOTRECTINIB
3.7%
of all REPOTRECTINIB reports
0
Deaths
1
Hospitalizations
How Dangerous Is Treatment noncompliance From REPOTRECTINIB?
Of the 7 reports, 1 (14.3%) required hospitalization.
Is Treatment noncompliance Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for REPOTRECTINIB. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does REPOTRECTINIB Cause?
Dizziness (32)
Death (21)
Nausea (12)
Adverse event (11)
Neuropathy peripheral (11)
Off label use (10)
Paraesthesia (10)
Balance disorder (9)
Pain (9)
Hospitalisation (8)
What Other Drugs Cause Treatment noncompliance?
CLOZAPINE (2,521)
RISPERIDONE (1,986)
APIXABAN (1,749)
ARIPIPRAZOLE (1,583)
NICOTINE (1,382)
PALIPERIDONE (1,218)
ISOTRETINOIN (905)
LENALIDOMIDE (780)
OLANZAPINE (765)
TREPROSTINIL (755)
Which REPOTRECTINIB Alternatives Have Lower Treatment noncompliance Risk?
REPOTRECTINIB vs REQUIP
REPOTRECTINIB vs RESLIZUMAB
REPOTRECTINIB vs RESMETIROM
REPOTRECTINIB vs RESTASIS
REPOTRECTINIB vs RETINOL