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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\GUAIFENESIN Cause Off label use? 21 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Off label use have been filed in association with ALBUTEROL\GUAIFENESIN. This represents 38.9% of all adverse event reports for ALBUTEROL\GUAIFENESIN.

21
Reports of Off label use with ALBUTEROL\GUAIFENESIN
38.9%
of all ALBUTEROL\GUAIFENESIN reports
2
Deaths
0
Hospitalizations

How Dangerous Is Off label use From ALBUTEROL\GUAIFENESIN?

Of the 21 reports, 2 (9.5%) resulted in death, and 1 (4.8%) were considered life-threatening.

Is Off label use Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ALBUTEROL\GUAIFENESIN. However, 21 reports have been filed with the FAERS database.

What Other Side Effects Does ALBUTEROL\GUAIFENESIN Cause?

Asthma (28) Food allergy (23) Hypersensitivity (23) Headache (22) Hepatic enzyme increased (22) Hyperhidrosis (22) Hypertension (22) Immunodeficiency (22) Infusion related reaction (22) Joint swelling (22)

What Other Drugs Cause Off label use?

RITUXIMAB (39,751) INFLIXIMAB (34,801) DENOSUMAB (34,612) METHOTREXATE (24,020) VEDOLIZUMAB (21,017) ETANERCEPT (20,178) TOCILIZUMAB (18,256) PREDNISONE (17,867) LENALIDOMIDE (17,017) ADALIMUMAB (16,417)

Related Pages

ALBUTEROL\GUAIFENESIN Full Profile All Off label use Reports All Drugs Causing Off label use ALBUTEROL\GUAIFENESIN Demographics