Does BUDESONIDE Cause Recalled product administered? 22 Reports in FDA Database
Boost Your Natural Energy & Metabolism
Mitolyn — 6 exotic plants to unlock your body's fat-burning power. 90-day guarantee.
According to the FDA Adverse Event Reporting System (FAERS), 22 reports of Recalled product administered have been filed in association with BUDESONIDE (BREYNA). This represents 0.1% of all adverse event reports for BUDESONIDE.
22
Reports of Recalled product administered with BUDESONIDE
0.1%
of all BUDESONIDE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Recalled product administered From BUDESONIDE?
Of the 22 reports.
Is Recalled product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE. However, 22 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 Recalled product administered?
RAMIPRIL (1,028)
LISINOPRIL (744)
PENICILLIN G BENZATHINE (500)
LEVOTHYROXINE (406)
HUMAN IMMUNOGLOBULIN G (382)
VARENICLINE (381)
VALSARTAN (267)
QUINAPRIL (243)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
Which BUDESONIDE Alternatives Have Lower Recalled product administered Risk?
BUDESONIDE vs BUDESONIDE\FORMOTEROL
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM
BUDESONIDE vs BUMETANIDE
BUDESONIDE vs BUPIVACAINE