Does ALBUTEROL Cause Condition aggravated? 2,815 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,815 reports of Condition aggravated have been filed in association with ALBUTEROL (Albuterol Sulfate). This represents 2.9% of all adverse event reports for ALBUTEROL.
2,815
Reports of Condition aggravated with ALBUTEROL
2.9%
of all ALBUTEROL reports
491
Deaths
1,518
Hospitalizations
How Dangerous Is Condition aggravated From ALBUTEROL?
Of the 2,815 reports, 491 (17.4%) resulted in death, 1,518 (53.9%) required hospitalization, and 531 (18.9%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALBUTEROL. However, 2,815 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which ALBUTEROL Alternatives Have Lower Condition aggravated Risk?
ALBUTEROL vs ALBUTEROL\BUDESONIDE
ALBUTEROL vs ALBUTEROL\IPRATROPIUM
ALBUTEROL vs ALCAFTADINE
ALBUTEROL vs ALCOHOL
ALBUTEROL vs ALCOHOL\CHLORHEXIDINE