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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 APREPITANT Cause Haemoglobin decreased? 43 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 43 reports of Haemoglobin decreased have been filed in association with APREPITANT (CINVANTI). This represents 0.8% of all adverse event reports for APREPITANT.

43
Reports of Haemoglobin decreased with APREPITANT
0.8%
of all APREPITANT reports
4
Deaths
28
Hospitalizations

How Dangerous Is Haemoglobin decreased From APREPITANT?

Of the 43 reports, 4 (9.3%) resulted in death, 28 (65.1%) required hospitalization, and 4 (9.3%) were considered life-threatening.

Is Haemoglobin decreased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for APREPITANT. However, 43 reports have been filed with the FAERS database.

What Other Side Effects Does APREPITANT Cause?

Fatigue (955) Pyrexia (913) Dyspnoea (909) Hypersensitivity (881) Rash (789) Alopecia (760) Gastrointestinal disorder (722) Pruritus (707) Confusional state (696) Glossodynia (696)

What Other Drugs Cause Haemoglobin decreased?

LENALIDOMIDE (4,031) RUXOLITINIB (3,297) ECULIZUMAB (3,028) ADALIMUMAB (2,459) CLOZAPINE (2,396) RITUXIMAB (1,803) APIXABAN (1,779) NIRAPARIB (1,759) METHOTREXATE (1,754) RIBAVIRIN (1,753)

Which APREPITANT Alternatives Have Lower Haemoglobin decreased Risk?

APREPITANT vs APROTININ APREPITANT vs ARANESP APREPITANT vs ARAVA APREPITANT vs AREDIA APREPITANT vs ARFORMOTEROL

Related Pages

APREPITANT Full Profile All Haemoglobin decreased Reports All Drugs Causing Haemoglobin decreased APREPITANT Demographics