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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 Post procedural complication? 35 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 35 reports of Post procedural complication have been filed in association with ALBUTEROL (Albuterol Sulfate). This represents 0.0% of all adverse event reports for ALBUTEROL.

35
Reports of Post procedural complication with ALBUTEROL
0.0%
of all ALBUTEROL reports
0
Deaths
20
Hospitalizations

How Dangerous Is Post procedural complication From ALBUTEROL?

Of the 35 reports, 20 (57.1%) required hospitalization, and 1 (2.9%) were considered life-threatening.

Is Post procedural complication Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ALBUTEROL. However, 35 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 Post procedural complication?

ADALIMUMAB (2,494) ETANERCEPT (318) CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (244) UPADACITINIB (241) RISANKIZUMAB-RZAA (232) INFLIXIMAB (217) METHOTREXATE (188) TREPROSTINIL (174) HUMAN IMMUNOGLOBULIN G (159) PREDNISONE (157)

Which ALBUTEROL Alternatives Have Lower Post procedural complication 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 Post procedural complication Reports All Drugs Causing Post procedural complication ALBUTEROL Demographics