Allegra and Singulair drug interactions - from FDA reports
Drug interactions are reported among people who take Allegra and Singulair together. This study is created by eHealthMe based on reports of 4,306 people who take Allegra and Singulair from FDA, and is updated regularly.
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4,306 people who take Allegra, Singulair are studied.
Number of reports submitted per year:
Most common drug interactions over time *:
< 1 month:
6 - 12 months:
1 - 2 years:
5 - 10 years:
Most common drug interactions by gender *:
Most common drug interactions by age *:
* Approximation only. Some reports may have incomplete information.
FDA reports used in this study
- Want to find out more about the FDA reports used in the study? You can request them from FDA.
Do you take Allegra and Singulair?
You are not alone:
Allegra has active ingredients of fexofenadine hydrochloride. It is often used in allergies. (latest outcomes from Allegra 51,818 users)
Singulair has active ingredients of montelukast sodium. It is often used in asthma. (latest outcomes from Singulair 78,334 users)
Interactions between Allegra and drugs from A to Za b c d e f g h i j k l m n o p q r s t u v w x y z
Interactions between Singulair and drugs from A to Za b c d e f g h i j k l m n o p q r s t u v w x y z
Browse all drug interactions of Allegra and Singulaira b c d e f g h i j k l m n o p q r s t u v w x y z
Related publications that referenced our studies
- Das S, Mondal S, Dey JK, Bandyopadhyay S, Saha I, Tripathi SK, "A case of montelukast induced hypercholesterolemia, severe hypertriglyceridemia and pancreatitis", Journal of Young Pharmacists, 2013 Jun .
What would happen?
Predict new side effects and undetected conditions when you take Allegra and Singulair (20,176 reports studied)
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NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT considered.
WARNING: Please DO NOT STOP MEDICATIONS without first consulting a physician since doing so could be hazardous to your health.
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You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).
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