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Singulair Related Oedema

Official Government Database Reports201
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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: Urticaria, Oedema

Posted By Anonymous in askapatient.com on February 27, 2015 @ 12:00 am

Side Effects: My feet were swollen have been off of it for 3 days still swollen. Hives all over my feet.

Druginformer Identified Side Effects: Tremor, Pain, Coordination abnormal, Oedema, Swelling

Posted By Anonymous in askapatient.com on May 1, 2014 @ 12:00 am

Gross edema (swelling) pain, Uncoordination and tremors. Mainly swelling. Still having it 5 days after stopping. It's significant though slightly better today (I've been taking Lasix ...

Druginformer Identified Side Effects: Arthralgia, Wheezing, Hunger, Abdominal discomfort, Abnormal weight gain, Nightmare, Abnormal dreams, Cough, Depression, Dyspnoea, Insomnia, Oedema, Rash, Suicidal ideation, Weight increased, Oropharyngeal pain

Posted By Anonymous in askapatient.com on July 28, 2011 @ 12:00 am

... I told the Doc and he said to go off for 4 days & try again. I started again after 5 days and the insomnia went away but the depression got worse and I began getting pain in my joints. I was always st...

Druginformer Identified Side Effects: Abnormal dreams, Asthma, Body temperature increased, Hyperhidrosis, Joint stiffness, Oedema, Swelling, Weight increased, Musculoskeletal discomfort, Poor quality sleep

Posted By Anonymous in askapatient.com on May 22, 2010 @ 12:00 am

Side Effects: Within days of starting Singulair granules: full-body edema (swelling), feverish for 18 hrs after taking med, sweating in sleep, weird dreams, poor sleep, legs so swollen they would ac...

Druginformer Identified Side Effects: Nausea, Depression, Oedema, Rash

Posted By Anonymous in askapatient.com on May 14, 2009 @ 12:00 am

... the problems to my working in the yard, so I focused on taking the Singulair more regularly, as my NP had advised when she gave me samples. I also began to feel mildly nauseated. My problems got rea...

Druginformer Identified Side Effects: Arthralgia, Fatigue, Sedation, Sleep disorder, Nightmare, Disturbance in attention, Fluid retention, Oedema, Somnolence

Posted By Anonymous in askapatient.com on July 12, 2007 @ 12:00 am

... symptoms from hell. Sleeping problems (nightmares and feeling like I had electicity running through my viens)Extreme drowsiness & sleepiness in the day, mental fogginess, bone and body aches so bad I ...

Druginformer Identified Side Effects: Back pain, Headache, Oedema, Weight increased

Posted By Anonymous in askapatient.com on May 15, 2007 @ 12:00 am

... in both feet and ankles. My supervisor at work asked me if I had broken my left foot and not known it. My knees are also swollen and I have started experiencing lower back pain. As seems to ...

Druginformer Identified Side Effects: Drug ineffective, Insomnia, Mood altered, Oedema

Posted By Anonymous in askapatient.com on August 20, 2006 @ 12:00 am

Side Effects: moodyness increased apitite puffiness in the face insomnia did not help my asthma at all


* 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.