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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 RISANKIZUMAB 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 RISANKIZUMAB (Skyrizi). This represents 0.5% of all adverse event reports for RISANKIZUMAB.

13
Reports of Haemoglobin decreased with RISANKIZUMAB
0.5%
of all RISANKIZUMAB reports
0
Deaths
9
Hospitalizations

How Dangerous Is Haemoglobin decreased From RISANKIZUMAB?

Of the 13 reports, 9 (69.2%) required hospitalization.

Is Haemoglobin decreased Listed in the Official Label?

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

What Other Side Effects Does RISANKIZUMAB Cause?

Product storage error (396) Drug ineffective (206) Psoriasis (138) Crohn's disease (103) Arthralgia (100) Off label use (100) Product temperature excursion issue (88) Diarrhoea (72) Fatigue (70) Rash (64)

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 RISANKIZUMAB Alternatives Have Lower Haemoglobin decreased Risk?

RISANKIZUMAB vs RISANKIZUMAB-RZAA RISANKIZUMAB vs RISDIPLAM RISANKIZUMAB vs RISEDRONATE RISANKIZUMAB vs RISEDRONIC ACID RISANKIZUMAB vs RISPERDAL

Related Pages

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