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Erythromycin Related Pain in extremity

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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: Arthralgia, Back pain, Fatigue, Pain, Myalgia, Abdominal pain upper, Pain in extremity, Abasia, Vaginitis bacterial

Posted By Anonymous in askapatient.com on January 9, 2014 @ 12:00 am

Side Effects: Starting Day 5 (unbearable by Day 6) stabbing pain in back, left side, stomach cramps, joint pain, extreme muscle pain in legs. knees so that I could not walk properly, extreme fatique,...

Druginformer Identified Side Effects: Chest pain, Back pain, Nausea, Musculoskeletal stiffness, Pain in extremity

Posted By Anonymous in askapatient.com on December 15, 2010 @ 12:00 am

Side Effects: excess saliva, nauseau chest pain, back stiffness, aching arms and hands It does appear to have started to resolve the infection on tonsils that was so bad I could not swallow...

Druginformer Identified Side Effects: Back pain, Headache, Pain, Diarrhoea, Discomfort, Micturition disorder, Pain in extremity, Pyrexia

Posted By Anonymous in askapatient.com on December 28, 2009 @ 12:00 am

Side Effects: Sickness and diarrhea, bloted painfull stomach, fever, headache, back and leg pain. I also Couldn't urinate for 3 days. i will never take this again. My chest infection was a ...


* 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.