Does ALBUTEROL Cause Intentional product use issue? 570 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 570 reports of Intentional product use issue have been filed in association with ALBUTEROL (Albuterol Sulfate). This represents 0.6% of all adverse event reports for ALBUTEROL.
570
Reports of Intentional product use issue with ALBUTEROL
0.6%
of all ALBUTEROL reports
31
Deaths
136
Hospitalizations
How Dangerous Is Intentional product use issue From ALBUTEROL?
Of the 570 reports, 31 (5.4%) resulted in death, 136 (23.9%) required hospitalization, and 25 (4.4%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALBUTEROL. However, 570 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which ALBUTEROL Alternatives Have Lower Intentional product use issue Risk?
ALBUTEROL vs ALBUTEROL\BUDESONIDE
ALBUTEROL vs ALBUTEROL\IPRATROPIUM
ALBUTEROL vs ALCAFTADINE
ALBUTEROL vs ALCOHOL
ALBUTEROL vs ALCOHOL\CHLORHEXIDINE