Does ALBUTEROL Cause Product complaint? 2,291 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,291 reports of Product complaint have been filed in association with ALBUTEROL (Albuterol Sulfate). This represents 2.4% of all adverse event reports for ALBUTEROL.
2,291
Reports of Product complaint with ALBUTEROL
2.4%
of all ALBUTEROL reports
9
Deaths
103
Hospitalizations
How Dangerous Is Product complaint From ALBUTEROL?
Of the 2,291 reports, 9 (0.4%) resulted in death, 103 (4.5%) required hospitalization, and 13 (0.6%) were considered life-threatening.
Is Product complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALBUTEROL. However, 2,291 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 Product complaint?
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (2,417)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (1,826)
FLUTICASONE\SALMETEROL (1,601)
MEPOLIZUMAB (1,296)
FLUTICASONE (1,112)
UMECLIDINIUM\VILANTEROL TRIFENATATE (1,108)
BELIMUMAB (1,079)
SUMATRIPTAN (718)
NICOTINE (700)
DICLOFENAC (511)
Which ALBUTEROL Alternatives Have Lower Product complaint Risk?
ALBUTEROL vs ALBUTEROL\BUDESONIDE
ALBUTEROL vs ALBUTEROL\IPRATROPIUM
ALBUTEROL vs ALCAFTADINE
ALBUTEROL vs ALCOHOL
ALBUTEROL vs ALCOHOL\CHLORHEXIDINE