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Ingredients: Erythromycin
Average User Review Score
* Based on 1 reviews from across the web.

Erythromycin is an antibiotic useful for the treatment of a number of bacterial infections. This includes respiratory tract infections, skin infections, chlamydia infections, and syphilis. It may also be used during pregnancy to prevent Group B streptococcal infection in the newborn. Erythromycin may be used to improve delayed stomach emptying. It can be given intravenously and by mouth. An eye ointment is routinely recommended after delivery to prevent eye infections in the newborn.

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Common adverse events from online conversations
Common adverse events from FDA database
* Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients.

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Druginformer Identified Side Effects: Abdominal discomfort

Posted By Anonymous in askapatient.com on November 29, 2007 @ 12:00 am

Side Effects: Mild stomach discomfort if taken on empty stomach. No other side effects. I have been taking this drug for several years now, with no ill effects. Liver functions are comple...

Druginformer Identified Side Effects: None

Posted By Berford2611 in twitter.com on June 15, 2014 @ 12:00 am

If it was out of play, it should only be a one-base advance and it's a dead ball, i.e., runner on 2nd gets 3rd.

Druginformer Identified Side Effects: None

Posted By Anonymous in facebook.com on March 10, 2008 @ 12:00 am

Vince Double You - Dancing With An Angel (Extended mix) Double You - Gimme All Your Love Double You - Got To Love Double You - Heart Of Glass Double You - Heart Of Glass (Club Mix) Double You - La Di ...

* 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.