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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does ALBUTEROL Cause Device use issue? 194 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 194 reports of Device use issue have been filed in association with ALBUTEROL (Albuterol Sulfate). This represents 0.2% of all adverse event reports for ALBUTEROL.

194
Reports of Device use issue with ALBUTEROL
0.2%
of all ALBUTEROL reports
0
Deaths
10
Hospitalizations

How Dangerous Is Device use issue From ALBUTEROL?

Of the 194 reports, 10 (5.2%) required hospitalization.

Is Device use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ALBUTEROL. However, 194 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 use issue?

SOMATROPIN (2,571) LEVONORGESTREL (2,489) COPPER (1,318) BUDESONIDE\FORMOTEROL (1,236) EXENATIDE (992) BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (976) DUPILUMAB (528) ALIROCUMAB (471) INSULIN GLARGINE (469) BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (459)

Which ALBUTEROL Alternatives Have Lower Device use issue Risk?

ALBUTEROL vs ALBUTEROL\BUDESONIDE ALBUTEROL vs ALBUTEROL\IPRATROPIUM ALBUTEROL vs ALCAFTADINE ALBUTEROL vs ALCOHOL ALBUTEROL vs ALCOHOL\CHLORHEXIDINE

Related Pages

ALBUTEROL Full Profile All Device use issue Reports All Drugs Causing Device use issue ALBUTEROL Demographics