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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 ABROCITINIB Cause Intentional dose omission? 10 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Intentional dose omission have been filed in association with ABROCITINIB (CIBINQO). This represents 0.3% of all adverse event reports for ABROCITINIB.

10
Reports of Intentional dose omission with ABROCITINIB
0.3%
of all ABROCITINIB reports
0
Deaths
1
Hospitalizations

How Dangerous Is Intentional dose omission From ABROCITINIB?

Of the 10 reports, 1 (10.0%) required hospitalization.

Is Intentional dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ABROCITINIB. However, 10 reports have been filed with the FAERS database.

What Other Side Effects Does ABROCITINIB Cause?

Drug ineffective (398) Condition aggravated (316) Off label use (269) Therapeutic product effect incomplete (186) Pruritus (171) Rash (134) Nausea (130) Dermatitis atopic (110) Headache (85) Acne (73)

What Other Drugs Cause Intentional dose omission?

DUPILUMAB (2,269) CERTOLIZUMAB PEGOL (1,253) ADALIMUMAB (845) TOFACITINIB (845) INFLIXIMAB (815) ABALOPARATIDE (623) ETANERCEPT (615) AMBRISENTAN (595) SODIUM OXYBATE (580) CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)

Which ABROCITINIB Alternatives Have Lower Intentional dose omission Risk?

ABROCITINIB vs ACALABRUTINIB ABROCITINIB vs ACAMPROSATE ABROCITINIB vs ACARBOSE ABROCITINIB vs ACCUTANE ABROCITINIB vs ACEBUTOLOL

Related Pages

ABROCITINIB Full Profile All Intentional dose omission Reports All Drugs Causing Intentional dose omission ABROCITINIB Demographics