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Erythromycin Related Skin tightness

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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: Pain, Anxiety, Skin tightness, Insomnia, Muscle spasms

Posted By Anonymous in askapatient.com on May 22, 2015 @ 12:00 am

Side Effects: Severe pain and cramp around torso below ribs. Made me anxious due to tightness and pain. Hard to sleep.

Druginformer Identified Side Effects: Flatulence, Pain, Burning sensation, Skin tightness, Abdominal pain upper, Diarrhoea, Drug ineffective, Decreased appetite, Oropharyngeal pain, Appetite disorder

Posted By Anonymous in askapatient.com on October 6, 2006 @ 12:00 am

Side Effects: No appetite. Burning Diarreah, Tons of painful farting and stomach cramps after eating. Upper abdominal tightness felt like stabbing pain Have had a sore throat, i was taking ...

Druginformer Identified Side Effects: Mouth ulceration, Decreased appetite, Pain, Lethargy, Sleep disorder, Skin tightness

Posted By Anonymous in askapatient.com on July 25, 2006 @ 12:00 am

Side Effects: Upper abdominal tightness, lack of appetite, general lethargy, mouth ulcers (worst of all), lack of sleep. This was prescribed to me as Im allergic to Penecillin and instructi...

* 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.