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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 CAPIVASERTIB Cause Intentional dose omission? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Intentional dose omission have been filed in association with CAPIVASERTIB (TRUQAP). This represents 0.3% of all adverse event reports for CAPIVASERTIB.

5
Reports of Intentional dose omission with CAPIVASERTIB
0.3%
of all CAPIVASERTIB reports
0
Deaths
2
Hospitalizations

How Dangerous Is Intentional dose omission From CAPIVASERTIB?

Of the 5 reports, 2 (40.0%) 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 CAPIVASERTIB. However, 5 reports have been filed with the FAERS database.

What Other Side Effects Does CAPIVASERTIB Cause?

Diarrhoea (278) Rash (253) Death (228) Hyperglycaemia (152) Nausea (96) Vomiting (81) Blood glucose increased (70) Fatigue (67) Malignant neoplasm progression (62) Disease progression (61)

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 CAPIVASERTIB Alternatives Have Lower Intentional dose omission Risk?

CAPIVASERTIB vs CAPLACIZUMAB CAPIVASERTIB vs CAPLACIZUMAB-YHDP CAPIVASERTIB vs CAPMATINIB CAPIVASERTIB vs CAPREOMYCIN CAPIVASERTIB vs CAPSAICIN

Related Pages

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