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Erythromycin Related Labour pain

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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: Headache, Dizziness, Vomiting, Abdominal pain upper, Discomfort, Insomnia, Muscular weakness, Labour pain

Posted By Anonymous in askapatient.com on August 28, 2013 @ 12:00 am

Side Effects: Stomach cramps like labour pain. Being sick, weak ,cant sleep, headache and dizzy. I just feel terrible don't ever take this antibiotics.

Druginformer Identified Side Effects: Pain, Lethargy, Abdominal distension, Abdominal pain upper, Diarrhoea, Dry mouth, Haemorrhage, Labour pain

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

Side Effects: Horrendous stomach cramps, extremely painful, i've given birth to three kids and these cramps felt worse than any ive ever experienced in my life including labour pains - started with t...

Druginformer Identified Side Effects: Abdominal discomfort, Hypersensitivity, Abdominal pain upper, Scar, Labour pain, Fear

Posted By Anonymous in askapatient.com on December 17, 2010 @ 12:00 am

Side Effects: Im allergic to penicillin so took these for 2 days but today think i will stop. I have had BAD BAD stomach pains since taking them. Last night i could not lie in bed as was jumping up e...

* 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.