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User Voices for Montelukast Sodium

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

Asthma

Side Effects: she is a high energy child who started experiencing very bad asthma and allergies at around 1 1/2 yrs. she was taking prednisone once a month for about 6 mos. and the dr. suggested sing...


Source: SINGULAIR: Side effects, ratings, and ...

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Asthma

Side Effects: Our son became irritable and gained 10 pounds! He had nightmares and threw temper tantrums. It did help his Asthma , but our sweet, loving boy became violent and out of control. The d...


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Asthma

... son is having severe tantrums, screaming, hitting, kicking, freaking out! He is also hallucinating. I take it also and have gained 15 pounds. Miserable. It does help with asthma , but not worth it. Bot...


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Asthma

... reason that he is beginning to fail in school. Not finish assignments, not turn work in, etc. Is this the medicine or just adolesence. The medicine has seemed to keep in asthma & allergy symptoms i...


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Asthma

Side Effects: My 2 year old son was diagnosed with Environmentally Induced Asthma in May 2006 (he was 19 months old). Smog and high humidity are the worst as are rapid chages in outdoor temperature. ...


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Asthma

Side Effects: Horrendous depression and crying. Really bummed about this because it's helped my asthma and shortness of breath a LOT. But I don't know how I can tolerate the depression much longer....


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Asthma

... days, requiring an emergency visit to a quick care facility where i was given hydrocodone and a shot of some painkiller. Aside from the side-effects, this medication treated my asthma and I didn't nee...


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Asthma

Side Effects: I developed a very bad allergic cough. My doctor actually thought I had developed asthma .

I was not given this drug for asthma and I am not an asthma sufferer so my experience...


Source: SINGULAIR: Side effects, ratings, and ...

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* 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.