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Erythromycin Related Sleep terror

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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: Tremor, Memory impairment, Confusional state, Pyrexia, Sleep terror, Somnolence

Posted By Anonymous in askapatient.com on August 20, 2011 @ 12:00 am

Side Effects: Confusion, Shakes, Tiredness, Forgetfulness (So bad, I couldn't remember my name and how to walk when I was out with my daughter.) Wind, Vivid Nightmares, and fever. This is m...

Druginformer Identified Side Effects: Sleep terror, Memory impairment, Candidiasis, Dyspepsia, Muscle spasms

Posted By Anonymous in askapatient.com on August 7, 2011 @ 12:00 am

Side Effects: vivid nightmares, cramps, upset stomach, thrush Taken this drug before and I don't remember it having this effect.

Druginformer Identified Side Effects: Retching, Tremor, Chest pain, Hunger, Nausea, Pain, Vomiting, Crying, Abdominal pain upper, Hyperhidrosis, Sleep terror

Posted By Anonymous in askapatient.com on February 25, 2011 @ 12:00 am

... terrible nightmares and was generally anxuous then awoke early in the morning with extreme stomach cramps and chest pain, vomiting for 4-6 hours to the point of dry heaving, sweating, trembling etc. L...


* 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.