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User Voices for Montelukast Sodium

The following are comments from users that experienced side effects while taking Montelukast Sodium

Abnormal Dreams

Helps. But have vivid dreams and night sweats on it.


Source: Singulair

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Night Sweats

Helps. But have vivid dreams and night sweats on it.


Source: Singulair

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Sinusitis

Can't complain...only 2 sinus infections a year vs the 16 in 18 moths 6 years ago


Source: Singulair

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Anxiety

Dr gave me Singulair . It does seem to help. I have a Medication Phobia so it is hard to take anything new. I suffer Hard Anxiety until I see I'm not having any adverse reactions


Source: Singulair

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Dry Skin

makes my throat a little dry, but works good


Source: Singulair

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Scar

I'm sorta scared since this was just in the news for suicide risk but I'm going to talk to my doctor about this.


Source: Singulair

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Somnolence

Makes you sleepy


Source: Singulair

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Mood Altered

Stopped taking on trial (month), was having problems sleeping, moody , etc. Now am more tired, but my cognitive thinking is better!


Source: Singulair

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Sleep Disorder

Stopped taking on trial (month), was having problems sleeping , moody, etc. Now am more tired, but my cognitive thinking is better!


Source: Singulair

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Fatigue

Stopped taking on trial (month), was having problems sleeping, moody, etc. Now am more tired , but my cognitive thinking is better!


Source: Singulair

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Cough

made her coughing go from 7 weeks to one


Source: Singulair

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Sneezing

I just started Singulair a couple of weeks ago and the results have been amazing. A lot less postnasal drip and sneezing , which were my main symptoms.


Source: Singulair

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* 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.