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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 ADAGRASIB Cause Condition aggravated? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Condition aggravated have been filed in association with ADAGRASIB (KRAZATI). This represents 0.6% of all adverse event reports for ADAGRASIB.

5
Reports of Condition aggravated with ADAGRASIB
0.6%
of all ADAGRASIB reports
3
Deaths
0
Hospitalizations

How Dangerous Is Condition aggravated From ADAGRASIB?

Of the 5 reports, 3 (60.0%) resulted in death, and 1 (20.0%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

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

What Other Side Effects Does ADAGRASIB Cause?

Death (272) Diarrhoea (113) Hospitalisation (108) Nausea (87) Vomiting (79) Off label use (70) Asthenia (61) Fatigue (51) Decreased appetite (43) Dehydration (35)

What Other Drugs Cause Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which ADAGRASIB Alternatives Have Lower Condition aggravated Risk?

ADAGRASIB vs ADALIMUMAB ADAGRASIB vs ADALIMUMAB-AACF ADAGRASIB vs ADALIMUMAB-AATY ADAGRASIB vs ADALIMUMAB-ADAZ ADAGRASIB vs ADALIMUMAB-ADBM

Related Pages

ADAGRASIB Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated ADAGRASIB Demographics