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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 TUCATINIB Cause Product residue present? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product residue present have been filed in association with TUCATINIB (TUKYSA). This represents 0.1% of all adverse event reports for TUCATINIB.

5
Reports of Product residue present with TUCATINIB
0.1%
of all TUCATINIB reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product residue present From TUCATINIB?

Of the 5 reports.

Is Product residue present Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TUCATINIB. However, 5 reports have been filed with the FAERS database.

What Other Side Effects Does TUCATINIB Cause?

Diarrhoea (1,587) Nausea (862) Fatigue (843) Vomiting (483) Death (400) Off label use (392) Malignant neoplasm progression (361) Palmar-plantar erythrodysaesthesia syndrome (355) Product dose omission issue (332) Asthenia (322)

What Other Drugs Cause Product residue present?

LEVODOPA (534) UPADACITINIB (442) ESTRADIOL (225) POTASSIUM (183) BUDESONIDE (168) MESALAMINE (156) MINOXIDIL (151) FEXOFENADINE\PSEUDOEPHEDRINE (149) TOFACITINIB (130) BUPROPION (123)

Which TUCATINIB Alternatives Have Lower Product residue present Risk?

TUCATINIB vs TUCIDINOSTAT TUCATINIB vs TYKERB TUCATINIB vs TYLENOL TUCATINIB vs TYROTHRICIN TUCATINIB vs TYSABRI

Related Pages

TUCATINIB Full Profile All Product residue present Reports All Drugs Causing Product residue present TUCATINIB Demographics