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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 EVEROLIMUS Cause Tumour marker increased? 228 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 228 reports of Tumour marker increased have been filed in association with EVEROLIMUS (EVEROLIMUS). This represents 0.6% of all adverse event reports for EVEROLIMUS.

228
Reports of Tumour marker increased with EVEROLIMUS
0.6%
of all EVEROLIMUS reports
13
Deaths
45
Hospitalizations

How Dangerous Is Tumour marker increased From EVEROLIMUS?

Of the 228 reports, 13 (5.7%) resulted in death, 45 (19.7%) required hospitalization, and 6 (2.6%) were considered life-threatening.

Is Tumour marker increased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for EVEROLIMUS. However, 228 reports have been filed with the FAERS database.

What Other Side Effects Does EVEROLIMUS Cause?

Death (5,090) Malignant neoplasm progression (3,789) Diarrhoea (3,061) Fatigue (2,946) Stomatitis (2,692) Nausea (2,079) Dyspnoea (1,925) Drug ineffective (1,837) Pyrexia (1,664) Decreased appetite (1,633)

What Other Drugs Cause Tumour marker increased?

PALBOCICLIB (817) FULVESTRANT (408) NIRAPARIB (356) LETROZOLE (343) RIBOCICLIB (317) RUCAPARIB CAMSYLATE (257) CAPECITABINE (228) ELACESTRANT (222) OLAPARIB (171) ANASTROZOLE (142)

Which EVEROLIMUS Alternatives Have Lower Tumour marker increased Risk?

EVEROLIMUS vs EVOLOCUMAB EVEROLIMUS vs EXELON EVEROLIMUS vs EXEMESTANE EVEROLIMUS vs EXENATIDE EVEROLIMUS vs EXFORGE

Related Pages

EVEROLIMUS Full Profile All Tumour marker increased Reports All Drugs Causing Tumour marker increased EVEROLIMUS Demographics