Does ALBUTEROL Cause Poor quality device used? 1,251 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,251 reports of Poor quality device used have been filed in association with ALBUTEROL (Albuterol Sulfate). This represents 1.3% of all adverse event reports for ALBUTEROL.
1,251
Reports of Poor quality device used with ALBUTEROL
1.3%
of all ALBUTEROL reports
2
Deaths
31
Hospitalizations
How Dangerous Is Poor quality device used From ALBUTEROL?
Of the 1,251 reports, 2 (0.2%) resulted in death, 31 (2.5%) required hospitalization, and 9 (0.7%) were considered life-threatening.
Is Poor quality device used Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALBUTEROL. However, 1,251 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 Poor quality device used?
SOMATROPIN (3,162)
MOMETASONE FUROATE (2,159)
FORMOTEROL\MOMETASONE FUROATE (1,091)
MEDROXYPROGESTERONE (80)
ETHINYL ESTRADIOL\ETONOGESTREL (77)
FOLLITROPIN (58)
ETONOGESTREL (55)
ETANERCEPT (46)
ESTRADIOL (41)
PEGFILGRASTIM (38)
Which ALBUTEROL Alternatives Have Lower Poor quality device used Risk?
ALBUTEROL vs ALBUTEROL\BUDESONIDE
ALBUTEROL vs ALBUTEROL\IPRATROPIUM
ALBUTEROL vs ALCAFTADINE
ALBUTEROL vs ALCOHOL
ALBUTEROL vs ALCOHOL\CHLORHEXIDINE