Erythromycin Related Musculoskeletal stiffness

Official Government Database Reports24

Online Conversations4

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, Malaise, Nausea, Hypersensitivity, Musculoskeletal stiffness, Diarrhoea, Somnolence, Decreased appetite

Posted By Anonymous in askapatient.com on October 8, 2013 @ 12:00 am

“Side Effects: Nausea for two hours after each dose, diarrhoea, stiff neck, headache, feeling of 'fullness' in ears, joint twinges, fatigue and general feeling of malaise. Having developed a...”

Druginformer Identified Side Effects: Chest discomfort, Back pain, Headache, Hunger, Nausea, Eye pain, Myalgia, Musculoskeletal stiffness, Crying, Abdominal pain upper, Dyspepsia, Dyspnoea, Muscular weakness

Posted By Anonymous in askapatient.com on March 14, 2013 @ 12:00 am

“Side Effects: Wind, Stomach Cramps, Upset Stomach, Constant need to go to the toilet, feeling very hungry but then felt nauseous, tight chest, difficulty breathing, weak, crying, headache, eyes hurt ...”

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: Dizziness, Nausea, Abdominal discomfort, Musculoskeletal stiffness

Posted By Anonymous in askapatient.com on October 28, 2005 @ 12:00 am

“Side Effects: dizziness, Nausea, stiff neck, severe stomach upset. Feel worse after taking Erythromycin.”

* 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.