Erythromycin Related Immobile

Official Government Database Reports3

Online Conversations3

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: Abdominal pain, Abdominal discomfort, Pain, Vomiting, Memory impairment, Immobile

Posted By Anonymous in askapatient.com on May 26, 2015 @ 12:00 am

“Side Effects: Had nagging pains in stomach all day Sunday (started taking them on saturday morning). Woke up at 3am Monday morning with severe stomach pains. Throwing up bile, literally as my body pr...”

Druginformer Identified Side Effects: Dizziness, Abdominal pain, Nausea, Vomiting, Immobile, Diarrhoea, Decreased appetite

Posted By Anonymous in askapatient.com on March 17, 2011 @ 12:00 am

“... I could not eat after because as I still felt the sharp pains as I would try to eat. Even after the 6 hours, if I moved around too fast I would soon hit the floor as the dizziness occured and would ta...”

Druginformer Identified Side Effects: Hunger, Nausea, Immobile, Dyspepsia

Posted By Anonymous in askapatient.com on August 6, 2007 @ 12:00 am

“Side Effects: Horrendous pains like heartburn, so bad I couldn't move or breathe and had to be taken to hospital. Intense hunger pains coupled with nausea. Wouldn't touch it again.”

* 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.