Does BUDESONIDE\FORMOTEROL Cause Decreased activity? 128 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 128 reports of Decreased activity have been filed in association with BUDESONIDE\FORMOTEROL. This represents 0.4% of all adverse event reports for BUDESONIDE\FORMOTEROL.
128
Reports of Decreased activity with BUDESONIDE\FORMOTEROL
0.4%
of all BUDESONIDE\FORMOTEROL reports
4
Deaths
73
Hospitalizations
How Dangerous Is Decreased activity From BUDESONIDE\FORMOTEROL?
Of the 128 reports, 4 (3.1%) resulted in death, 73 (57.0%) required hospitalization, and 2 (1.6%) were considered life-threatening.
Is Decreased activity Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE\FORMOTEROL. However, 128 reports have been filed with the FAERS database.
What Other Side Effects Does BUDESONIDE\FORMOTEROL Cause?
Dyspnoea (11,158)
Asthma (10,045)
Wheezing (5,632)
Cough (4,466)
Therapeutic product effect incomplete (4,392)
Drug ineffective (3,469)
Intentional product misuse (3,399)
Loss of personal independence in daily activities (3,397)
Off label use (3,269)
Device malfunction (2,771)
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 BUDESONIDE\FORMOTEROL Alternatives Have Lower Decreased activity Risk?
BUDESONIDE\FORMOTEROL vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE
BUDESONIDE\FORMOTEROL vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM
BUDESONIDE\FORMOTEROL vs BUMETANIDE
BUDESONIDE\FORMOTEROL vs BUPIVACAINE
BUDESONIDE\FORMOTEROL vs BUPIVACAINE\BUPIVACAINE ANHYDROUS