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Erythromycin Related Accidental poisoning

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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: Retching, Abdominal pain upper, Accidental poisoning, Discomfort

Posted By Anonymous in askapatient.com on September 8, 2015 @ 12:00 am

Side Effects: Bad stomach cramps. Dry heaving until eventually bile came up. Haven't eaten since I was sick and can't face the thought of food. Never had a reaction to ab's before. This is like takin...

Druginformer Identified Side Effects: Headache, Fatigue, Dizziness, Nausea, Vomiting, Gastrointestinal pain, Accidental poisoning, Heart rate irregular, Pyrexia

Posted By Anonymous in askapatient.com on August 13, 2011 @ 12:00 am

Side Effects: Extreme intestinal pain.nausea followed by vomiting.Irregular heartbeat.fever,headache,dizziness and extreme fatigue four weeks later Toxic,poisonous muck

Druginformer Identified Side Effects: Chest pain, Fatigue, Dizziness, Nausea, Vomiting, Abdominal pain lower, Accidental poisoning, Dyspepsia, Muscular weakness, Tenderness, Decreased appetite

Posted By Anonymous in askapatient.com on March 31, 2011 @ 12:00 am

... supposed to be 7 days but had to stop due to: Severe lower abdominal pain Constant nausea leading to vomiting Dizziness Chest pain Constant heartburn Stomach soreness Significantly reduced appe...

* 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.