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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 PEXIDARTINIB Cause Haemoglobin decreased? 13 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Haemoglobin decreased have been filed in association with PEXIDARTINIB (Turalio). This represents 1.3% of all adverse event reports for PEXIDARTINIB.

13
Reports of Haemoglobin decreased with PEXIDARTINIB
1.3%
of all PEXIDARTINIB reports
0
Deaths
3
Hospitalizations

How Dangerous Is Haemoglobin decreased From PEXIDARTINIB?

Of the 13 reports, 3 (23.1%) required hospitalization.

Is Haemoglobin decreased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PEXIDARTINIB. However, 13 reports have been filed with the FAERS database.

What Other Side Effects Does PEXIDARTINIB Cause?

Fatigue (378) Product dose omission issue (335) Hair colour changes (327) Nausea (213) Pruritus (186) Aspartate aminotransferase increased (134) Rash (131) Off label use (130) Alanine aminotransferase increased (124) Diarrhoea (106)

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 PEXIDARTINIB Alternatives Have Lower Haemoglobin decreased Risk?

PEXIDARTINIB vs PHENACETIN PEXIDARTINIB vs PHENAZOPYRIDINE PEXIDARTINIB vs PHENCYCLIDINE PEXIDARTINIB vs PHENELZINE PEXIDARTINIB vs PHENOBARBITAL

Related Pages

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