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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 mechanical issue? 455 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 455 reports of Device mechanical issue have been filed in association with ALBUTEROL (Albuterol Sulfate). This represents 0.5% of all adverse event reports for ALBUTEROL.

455
Reports of Device mechanical issue with ALBUTEROL
0.5%
of all ALBUTEROL reports
0
Deaths
8
Hospitalizations

How Dangerous Is Device mechanical issue From ALBUTEROL?

Of the 455 reports, 8 (1.8%) required hospitalization, and 1 (0.2%) were considered life-threatening.

Is Device mechanical issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ALBUTEROL. However, 455 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 mechanical issue?

SOMATROPIN (6,411) INSULIN GLARGINE-YFGN (853) INSULIN GLARGINE (725) DEVICE (226) ETANERCEPT (145) FLUTICASONE\SALMETEROL (127) GLATIRAMER (124) EXENATIDE (108) MEDROXYPROGESTERONE (99) ADALIMUMAB-AFZB (76)

Which ALBUTEROL Alternatives Have Lower Device mechanical 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 mechanical issue Reports All Drugs Causing Device mechanical issue ALBUTEROL Demographics