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Singulair Related Somnolence

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Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients. To view the active ingredient report, please click here.

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Druginformer Identified Side Effects: Back pain, Fatigue, Sinusitis, Cardiac flutter, Skin tightness, Hip fracture, Irritability, Nasal congestion, Somnolence

Posted By Anonymous in askapatient.com on February 8, 2015 @ 12:00 am

... But I started having heart palpitations as soon as I started taking it, was always tired and sleepy (was sleeping as much as 12 hours a night), had hip pain, lower back pain, pain and tightness in my ...

Druginformer Identified Side Effects: Coma, Depression, Somnolence

Posted By Anonymous in fdb.rxlist.com on December 24, 2014 @ 12:00 am

I was taking this daily, few years back and would get extremely sleepy and depressed, although cleared symptoms my sister who is approx. 8 years older went into a coma last year for 5 days and they s...

Druginformer Identified Side Effects: Somnolence, Chest discomfort, Dizziness, Nightmare, Anxiety, Depression

Posted By Anonymous in askapatient.com on September 23, 2014 @ 12:00 am

Side Effects: Sleepy, dizzy. Transient. I was told to take this drug at bedtime for those reasons. I haven't noticed anxiety, depression. Or any more nightmares than my usual, what I do experience is...

Druginformer Identified Side Effects: Arthralgia, Back pain, Headache, Neck pain, Fatigue, Abnormal dreams, Somnolence

Posted By Anonymous in askapatient.com on July 8, 2014 @ 12:00 am

... are better than when on an antihistamine and cortisol steroid inhaler combo regimen. I am a bit tired during the day but I can accept this, the odd dreams, and the minor aches and pains since I can b...

Druginformer Identified Side Effects: Headache, Dizziness, Nausea, Abdominal discomfort, Sleep disorder, Anxiety, Aggression, Apathy, Depression, Insomnia, Muscular weakness, Somnolence, Hot flush, Decreased appetite

Posted By Anonymous in askapatient.com on May 21, 2014 @ 12:00 am

Side Effects: loss of appetite, nausea, stomach pains, insomnia, interrupted sleep, anxiety, pain and weakness in arm, fatigue, headaches, feeling disconnected, heat flashes, dizziness, aggression, d...

Druginformer Identified Side Effects: Headache, Insomnia, Somnolence

Posted By Anonymous in askapatient.com on March 24, 2014 @ 12:00 am

Side Effects: The worst insomnia imaginable(it's 5:01 as I write this and I've been trying to sleep since 10:30p), and a fatigue headache to match. Pretty much unbearable. Have noticed slight reducti...

Druginformer Identified Side Effects: Nightmare, Memory impairment, Hyperventilation, Abnormal dreams, Drug ineffective, Paraesthesia, Somnolence, Poor quality sleep

Posted By Anonymous in askapatient.com on January 2, 2014 @ 12:00 am

... time of the day that I was taking it, and it didn't help. I came across these pills last night and decided to try one, not remembering if this was the medicine that caused the nightmares (I've tried a...

Druginformer Identified Side Effects: Cough, Somnolence

Posted By Anonymous in askapatient.com on November 24, 2013 @ 12:00 am

Side Effects: He has less coughing, sleepyness, he ha been using it since he was two. Without it it is non stop coughing.

Druginformer Identified Side Effects: Depression, Somnolence

Posted By DannyVirgo in fdb.rxlist.com on July 17, 2013 @ 12:00 am

... and the generic Singulair is the ONLY thing that has helped- Pulmicort, advair, etc. However, I have experienced the WORSE side effects ever! Last year I became extremely depressed but blamed it on li...

Druginformer Identified Side Effects: Cardiac flutter, Pyrexia, Somnolence

Posted By Anonymous in drugs.com on June 17, 2013 @ 12:00 am

... really bad cedar fever which is a problem in Texas. I am a rather slim female and at first my doctor gave me the regular adult dosage. It was too strong. I had heart palpitations and almost called ...

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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.