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Erythromycin Related Disability

Official Government Database Reports16
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: Eructation, Abdominal pain, Nausea, Vomiting, Disability, Drug ineffective

Posted By Anonymous in askapatient.com on March 23, 2015 @ 12:00 am

Side Effects: Severe debilitating upper abdomen pain through back. Pulsating stomach muscles. Feelings of nausea but no actual vomit. Excessive burping. After taking only 1 pill approximate...

Druginformer Identified Side Effects: Chest pain, Headache, Abdominal pain, Hunger, Disability, Muscle spasms

Posted By Anonymous in askapatient.com on March 2, 2012 @ 12:00 am

Side Effects: Severe debilitating abdo cramps (feels like it's right by my diaphragm), chest pain, headache, hollow hungry feeling but cramping too severe to eat. When I first felt the seve...

Druginformer Identified Side Effects: Disability, Flatulence, Abdominal pain, Nausea, Abdominal distension, Aggression

Posted By Anonymous in askapatient.com on September 9, 2005 @ 12:00 am

... abdominal cramps and nausea, extreme gaseous bloating aggressive 500 mg 4x daily. I felt like my stomach was wrapped in "barbed wire"...this feeling is more debilitating than the condition. ...

* 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.