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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 RAMUCIRUMAB Cause Adverse event? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Adverse event have been filed in association with RAMUCIRUMAB (CYRAMZA). This represents 0.1% of all adverse event reports for RAMUCIRUMAB.

6
Reports of Adverse event with RAMUCIRUMAB
0.1%
of all RAMUCIRUMAB reports
3
Deaths
0
Hospitalizations

How Dangerous Is Adverse event From RAMUCIRUMAB?

Of the 6 reports, 3 (50.0%) resulted in death.

Is Adverse event Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RAMUCIRUMAB. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does RAMUCIRUMAB Cause?

Malignant neoplasm progression (743) Death (492) Interstitial lung disease (269) Febrile neutropenia (229) Neutropenia (229) Decreased appetite (187) Diarrhoea (186) Hypertension (175) Pyrexia (161) Nausea (160)

What Other Drugs Cause Adverse event?

ABATACEPT (4,028) APIXABAN (3,871) ETANERCEPT (3,096) LENALIDOMIDE (2,426) INFLIXIMAB (2,269) ADALIMUMAB (2,121) METHOTREXATE (1,846) LEFLUNOMIDE (1,476) RIVAROXABAN (1,465) ALENDRONATE (1,462)

Which RAMUCIRUMAB Alternatives Have Lower Adverse event Risk?

RAMUCIRUMAB vs RANEXA RAMUCIRUMAB vs RANIBIZUMAB RAMUCIRUMAB vs RANIMUSTINE RAMUCIRUMAB vs RANITIDINE RAMUCIRUMAB vs RANITIDINE\RANITIDINE

Related Pages

RAMUCIRUMAB Full Profile All Adverse event Reports All Drugs Causing Adverse event RAMUCIRUMAB Demographics