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Singulair Related Heart rate increased

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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: Headache, Fatigue, Abdominal pain, Hunger, Vomiting, Nightmare, Mood swings, Disturbance in attention, Drug ineffective, Dyspepsia, Heart rate increased, Migraine, Pain in extremity, Rash, Vaginal haemorrhage, Psychotic disorder

Posted By Anonymous in askapatient.com on June 13, 2008 @ 12:00 am

... she has only had one or two good days a week. She completely missed the last semester of the 11th grade and will have to repeat it. Her symptoms have been: headaches (cluster, migraine and mild), le...

Druginformer Identified Side Effects: Fatigue, Dizziness, Nausea, Vomiting, Nightmare, Memory impairment, Anxiety, Premenstrual syndrome, Decreased interest, Depression, Discomfort, Heart rate increased, Hypertension, Insomnia, Irritability, Migraine, Suicidal ideation, Weight decreased

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

... nightmares, insomnia, irritability, constant PMS type symptoms, migraines (sick migraines - puking), dizziness, nausea, forgetfulness, anxiety, rapid heartbeat, exhaustion, loss of interest. ...

Druginformer Identified Side Effects: Constipation, Pain, Flushing, Depression, Disturbance in attention, Dry mouth, Heart rate increased, Tachypnoea

Posted By Anonymous in askapatient.com on May 30, 2007 @ 12:00 am

... great feelings of depression, just wanted to stop my day and sleep. Hard to concentrate, and get motivated. Feeling flush faced, with rapid breathing, dry mouth. Lots of constipation. Feeling of w...

* 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.