Does ALBUTEROL Cause Device breakage? 256 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 256 reports of Device breakage have been filed in association with ALBUTEROL (Albuterol Sulfate). This represents 0.3% of all adverse event reports for ALBUTEROL.
256
Reports of Device breakage with ALBUTEROL
0.3%
of all ALBUTEROL reports
0
Deaths
12
Hospitalizations
How Dangerous Is Device breakage From ALBUTEROL?
Of the 256 reports, 12 (4.7%) required hospitalization, and 4 (1.6%) were considered life-threatening.
Is Device breakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALBUTEROL. However, 256 reports have been filed with the FAERS database.
What Other Side Effects Does ALBUTEROL Cause?
Dyspnoea (21,856)
Asthma (18,997)
Wrong technique in product usage process (17,114)
Wheezing (11,555)
Drug ineffective (11,057)
Device delivery system issue (9,509)
No adverse event (8,971)
Therapeutic product effect incomplete (8,496)
Cough (8,355)
Drug dose omission by device (8,162)
What Other Drugs Cause Device breakage?
COPPER (9,201)
SOMATROPIN (7,761)
ETONOGESTREL (4,140)
LEVONORGESTREL (2,726)
ETHINYL ESTRADIOL\ETONOGESTREL (741)
CARBIDOPA\LEVODOPA (634)
TREPROSTINIL (396)
ADALIMUMAB (375)
EPOPROSTENOL (240)
INSULIN GLARGINE (237)
Which ALBUTEROL Alternatives Have Lower Device breakage Risk?
ALBUTEROL vs ALBUTEROL\BUDESONIDE
ALBUTEROL vs ALBUTEROL\IPRATROPIUM
ALBUTEROL vs ALCAFTADINE
ALBUTEROL vs ALCOHOL
ALBUTEROL vs ALCOHOL\CHLORHEXIDINE