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Erythromycin Related Thought blocking

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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: Abdominal discomfort, Lethargy, Abdominal pain upper, Dizziness, Hunger, Thought blocking, Tooth abscess

Posted By Anonymous in askapatient.com on September 17, 2011 @ 12:00 am

Side Effects: Dizziness lethargy sickness stomach cramps Started taking this yesterday , this morning my stomach was churning , I felt hungry but sick at the same time , my eyes couldn'...

Druginformer Identified Side Effects: Asthenia, Arthralgia, Dizziness, Nausea, Vomiting, Lethargy, Abdominal pain upper, Confusional state, Irritability, Somnolence, Thought blocking, Emotional distress, Decreased appetite

Posted By Anonymous in askapatient.com on April 9, 2010 @ 12:00 am

Side Effects: Extreme nausea, stomach cramps, loss of appetite, aching joints & general weakness/lethargy, extreme tiredness, emotionally unstable/ irritable, vomiting, feeling 'spaced-out', difficul...

Druginformer Identified Side Effects: Fatigue, Pain, Hypersensitivity, Insomnia, Muscular weakness, Thought blocking

Posted By Anonymous in askapatient.com on June 29, 2009 @ 12:00 am

Side Effects: Whole leg and arm weakness, couldn't sleep or eat. Body exhausted. Couldn't think or remember names. Spent 4 days in bed. a excrutiating pains in upper back calf.Took 3 paracetomol to g...

Druginformer Identified Side Effects: Pain, Vomiting, Thought blocking, Adverse drug reaction

Posted By Anonymous in askapatient.com on September 10, 2006 @ 12:00 am

... large amounts of food did the yogurt thing and the side effects are still the same. I even dropped dosage to 1500mg and no change of side effects severe UN-GODLY pain in upper abdomin around...

* 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.