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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 BELUMOSUDIL Cause Decreased activity? 13 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Decreased activity have been filed in association with BELUMOSUDIL (Rezurock). This represents 0.5% of all adverse event reports for BELUMOSUDIL.

13
Reports of Decreased activity with BELUMOSUDIL
0.5%
of all BELUMOSUDIL reports
0
Deaths
4
Hospitalizations

How Dangerous Is Decreased activity From BELUMOSUDIL?

Of the 13 reports, 4 (30.8%) required hospitalization.

Is Decreased activity Listed in the Official Label?

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

What Other Side Effects Does BELUMOSUDIL Cause?

Inappropriate schedule of product administration (377) Product use in unapproved indication (340) Fatigue (246) Nausea (154) Product dose omission issue (143) Drug ineffective (141) Diarrhoea (136) Death (135) Condition aggravated (127) Off label use (124)

What Other Drugs Cause Decreased activity?

NIRAPARIB (586) SACUBITRIL\VALSARTAN (570) RUXOLITINIB (558) DUPILUMAB (231) LEVOTHYROXINE (201) TREPROSTINIL (195) PREDNISONE (193) ALBUTEROL (190) EMTRICITABINE\TENOFOVIR DISOPROXIL (186) TERIPARATIDE (156)

Which BELUMOSUDIL Alternatives Have Lower Decreased activity Risk?

BELUMOSUDIL vs BELVIQ BELUMOSUDIL vs BELZUTIFAN BELUMOSUDIL vs BEMPEDOIC ACID BELUMOSUDIL vs BEMPEDOIC ACID\EZETIMIBE BELUMOSUDIL vs BEMPEGALDESLEUKIN

Related Pages

BELUMOSUDIL Full Profile All Decreased activity Reports All Drugs Causing Decreased activity BELUMOSUDIL Demographics