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Erythromycin Related Hiccups

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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: Tremor, Headache, Fatigue, Dizziness, Hunger, Hiccups, Hypersensitivity, Cardiovascular disorder, Abscess, Cardiac flutter, Dyspepsia, Gastrointestinal disorder, Oedema, Decreased appetite

Posted By Anonymous in askapatient.com on November 27, 2011 @ 12:00 am

Side Effects: headache, dizziness, ravenously hungry, inability to eat, heart palpitations, extreme fatigue, shakiness, hiccups, swollen feet, severe indigestion I am allergic to penicillin...

Druginformer Identified Side Effects: Nausea, Abdominal discomfort, Hiccups, Euphoric mood, Tonsillitis, Diarrhoea

Posted By Anonymous in askapatient.com on September 15, 2011 @ 12:00 am

Side Effects: Severe Nausea, Stomach Pain, Lightheaded, Diarrhea, Hiccups I think I'd much rather take my chances with my tonsils blocking off my airway than subject myself to the side effe...

Druginformer Identified Side Effects: Malaise, Vomiting, Hiccups, Abdominal distension, Abdominal pain upper

Posted By Anonymous in askapatient.com on May 18, 2010 @ 12:00 am

Side Effects: Felt a bit sick when i woke up this morning after starting my prescription last night. As today went on i started experiencing extreme stomach cramps. The cramps were intermitant, usual...

* 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.