Does BUDESONIDE\FORMOTEROL Cause Product packaging quantity issue? 301 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 301 reports of Product packaging quantity issue have been filed in association with BUDESONIDE\FORMOTEROL. This represents 0.8% of all adverse event reports for BUDESONIDE\FORMOTEROL.
301
Reports of Product packaging quantity issue with BUDESONIDE\FORMOTEROL
0.8%
of all BUDESONIDE\FORMOTEROL reports
2
Deaths
41
Hospitalizations
How Dangerous Is Product packaging quantity issue From BUDESONIDE\FORMOTEROL?
Of the 301 reports, 2 (0.7%) resulted in death, 41 (13.6%) required hospitalization, and 4 (1.3%) were considered life-threatening.
Is Product packaging quantity issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE\FORMOTEROL. However, 301 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 Product packaging quantity issue?
LEUPROLIDE (523)
ALBUTEROL (431)
FENTANYL (286)
BUPRENORPHINE (225)
CYCLOSPORINE (206)
ESTRADIOL (201)
BIMATOPROST (177)
RIVAROXABAN (174)
EXENATIDE (154)
LIFITEGRAST (153)
Which BUDESONIDE\FORMOTEROL Alternatives Have Lower Product packaging quantity issue 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