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Montelukast

Ingredients: Montelukast Sodium
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* Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients.

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Druginformer Identified Side Effects: Fatigue, Ear pain, Thirst

Effectiveness Rating:     Overall Rating:

Posted By deborah on October 18, 2018 @ 12:23 pm

wonder if its woth feeling like this on these tablets chest so much better but i have no energy terrible ear pains mainly at night and drinking a lot of wate

Druginformer Identified Side Effects: Dry skin, Dreamy state, Dehydration

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Posted By Jane on March 17, 2017 @ 3:14 am

Dreams are not bad, just different. My face is so dry that I've had to apply a combination of lubriderm lotion, coconut oil, and vitamin e oil twice a day, generously, to get it back to normal. It's so dry that it soaks all of that up and I'm still not shiny or oily looking. Before this moisturizing regimen, my skin has red blotches where skin was flaking. I've been drinking a couple liters of water a day (mostly in the evenings) and still fibs my self feeling very thirsty while I'm asleep, even waking up from dry throat.

Druginformer Identified Side Effects: Sleep disorder, Abnormal dreams, Mood altered, Hyperhidrosis

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Posted By Anthony on October 1, 2016 @ 7:02 am

Effective against allergen triggered asthma. However, sleep disrupted, waking in the middle of the night, vivid dreams and night sweats. Also a depressant.


* Warning: The facts and figures contained in these reports are accurate to the best of our capability; however, our metrics are only meant to augment your medical knowledge, and should never be used as the sole basis for selecting a new medication. As with any medical decision, be sure to work with your doctor to ensure the best choices are made for your condition.

* About FAERS: The FDA Adverse Event Reporting System (FAERS) is used by FDA for activities such as looking for new safety concerns that might be related to a marketed product, evaluating a manufacturer's compliance to reporting regulations and responding to outside requests for information. Reporting of adverse events is a voluntary process, and not every report is sent to FDA and entered into FAERS. The FAERS database may contain duplicate reports, the report quality is variable, and many factors may influence reporting (e.g., media attention, length of time a drug is marketed, market share). For these reasons, FAERS case reports cannot be used to calculate incidence or estimates of risk for a particular product or compare risks between products.