Does BUDESONIDE Cause Wrong technique in product usage process? 242 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 242 reports of Wrong technique in product usage process have been filed in association with BUDESONIDE (BREYNA). This represents 1.0% of all adverse event reports for BUDESONIDE.
242
Reports of Wrong technique in product usage process with BUDESONIDE
1.0%
of all BUDESONIDE reports
2
Deaths
17
Hospitalizations
How Dangerous Is Wrong technique in product usage process From BUDESONIDE?
Of the 242 reports, 2 (0.8%) resulted in death, 17 (7.0%) required hospitalization, and 2 (0.8%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE. However, 242 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which BUDESONIDE Alternatives Have Lower Wrong technique in product usage process Risk?
BUDESONIDE vs BUDESONIDE\FORMOTEROL
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM
BUDESONIDE vs BUMETANIDE
BUDESONIDE vs BUPIVACAINE