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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 information output issue? 318 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 318 reports of Device information output issue have been filed in association with ALBUTEROL (Albuterol Sulfate). This represents 0.3% of all adverse event reports for ALBUTEROL.

318
Reports of Device information output issue with ALBUTEROL
0.3%
of all ALBUTEROL reports
0
Deaths
0
Hospitalizations

How Dangerous Is Device information output issue From ALBUTEROL?

Of the 318 reports.

Is Device information output issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ALBUTEROL. However, 318 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 information output issue?

SOMATROPIN (5,220) TREPROSTINIL (141) CARBIDOPA\LEVODOPA (14) INSULIN ASPART (10) DEVICE (9) BUDESONIDE\FORMOTEROL (7) ETANERCEPT (7) NOREPINEPHRINE (6) BACLOFEN (5) ESTRADIOL (5)

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