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Erythromycin Related Mental impairment

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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: Arthralgia, Chest pain, Headache, Fatigue, Erythema, Pain, Pruritus, Burning sensation, Myalgia, Palpitations, Anxiety, Abdominal pain upper, Abnormal dreams, Confusional state, Insomnia, Irritability, Mental impairment, Tenderness, Decreased appetite, Menstruation irregular

Posted By Anonymous in askapatient.com on December 14, 2012 @ 12:00 am

itchy red bumps on my chest, confusion, extreme fatigue, gums became red, very sore and throbbed so bad it hurt to eat, heart palps, confusion, anxiety and very irritated. No patience w...

Druginformer Identified Side Effects: Tremor, Chest pain, Sedation, Anxiety, Mental impairment, Decreased appetite

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

... to the out of hours doctors she said i had suspected phuemonia I ended up having to be taken to hospital the night before last i was so distressed no one could calm me down i was shaking so much the m...

Druginformer Identified Side Effects: Dizziness, Dry mouth, Mental impairment, Mouth ulceration, Delayed sleep phase

Posted By Anonymous in askapatient.com on September 22, 2006 @ 12:00 am

Side Effects: dizziness, unable to focus my thoughts, taking a long time to fall asleep at night (several hours), mouth ulcers, dry mouth

Druginformer Identified Side Effects: Lethargy, Impatience, Abdominal pain upper, Disturbance in attention, Mental impairment, Somnolence

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

Side Effects: Stomach cramps, mental difficulties - loss of concentration, lethargy, sleepy, aggravated, impatience

* 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.