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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 RITLECITINIB Cause Haemoglobin decreased? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Haemoglobin decreased have been filed in association with RITLECITINIB (Litfulo). This represents 0.4% of all adverse event reports for RITLECITINIB.

5
Reports of Haemoglobin decreased with RITLECITINIB
0.4%
of all RITLECITINIB reports
0
Deaths
1
Hospitalizations

How Dangerous Is Haemoglobin decreased From RITLECITINIB?

Of the 5 reports, 1 (20.0%) required hospitalization.

Is Haemoglobin decreased Listed in the Official Label?

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

What Other Side Effects Does RITLECITINIB Cause?

Drug ineffective (259) Therapeutic product effect incomplete (122) Condition aggravated (85) Off label use (82) Headache (70) Diarrhoea (49) Product dose omission issue (45) Alopecia (44) Fatigue (36) Urticaria (36)

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 RITLECITINIB Alternatives Have Lower Haemoglobin decreased Risk?

RITLECITINIB vs RITODRINE RITLECITINIB vs RITONAVIR RITLECITINIB vs RITUXAN RITLECITINIB vs RITUXIMAB RITLECITINIB vs RITUXIMAB-ABBS

Related Pages

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