Does BUDESONIDE Cause Haemoglobin decreased? 69 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 69 reports of Haemoglobin decreased have been filed in association with BUDESONIDE (BREYNA). This represents 0.3% of all adverse event reports for BUDESONIDE.
69
Reports of Haemoglobin decreased with BUDESONIDE
0.3%
of all BUDESONIDE reports
2
Deaths
49
Hospitalizations
How Dangerous Is Haemoglobin decreased From BUDESONIDE?
Of the 69 reports, 2 (2.9%) resulted in death, 49 (71.0%) required hospitalization, and 3 (4.3%) 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 BUDESONIDE. However, 69 reports have been filed with the FAERS database.
What Other Side Effects Does BUDESONIDE Cause?
Asthma (4,544)
Dyspnoea (4,441)
Drug ineffective (4,384)
Off label use (3,033)
Wheezing (2,590)
Cough (2,269)
Therapeutic product effect incomplete (2,191)
Loss of personal independence in daily activities (1,890)
Condition aggravated (1,548)
Fatigue (1,508)
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 BUDESONIDE Alternatives Have Lower Haemoglobin decreased Risk?
BUDESONIDE vs BUDESONIDE\FORMOTEROL
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM
BUDESONIDE vs BUMETANIDE
BUDESONIDE vs BUPIVACAINE