DrugInformer Search

Erythromycin Related Tinnitus

Official Government Database Reports36
Online Conversations7

Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients. To view the active ingredient report, please click here.

Tell us about your Experience with Erythromycin

Thank you for sharing your experience with us!

Share Your Experience

Druginformer Identified Side Effects: Headache, Fatigue, Nausea, Pain, Tinnitus, Abnormal dreams, Diarrhoea, Drug ineffective, Insomnia, Decreased appetite

Posted By Anonymous in askapatient.com on March 13, 2013 @ 12:00 am

... but didn't make connection with that and other symptoms of extreme nausea, loss of appetite, inability to sleep and when sleep came from exhaustion disturbing dreams, headache, acute pain behind right...

Druginformer Identified Side Effects: Chest pain, Back pain, Dizziness, Feeling abnormal, Tinnitus, Anxiety, Deafness, Depression, Heart rate irregular, Insomnia, Scar, Fear

Posted By Anonymous in askapatient.com on January 5, 2011 @ 12:00 am

Side Effects: Fast heart beat, chest pain, shooting back pain, depression, anxiety, fearful - scared feeling, unexplained fear of usual events or tv shows, spaced out feeling, dizzy, LOUD ringing in ...

Druginformer Identified Side Effects: Lethargy, Nightmare, Tinnitus, Confusional state, Depression, Diarrhoea, Disturbance in attention, Dyspepsia, Somnolence, Decreased appetite, Fear

Posted By Anonymous in askapatient.com on August 22, 2009 @ 12:00 am

Side Effects: In the first few weeks: indigestion, lack of appetite, diarrhea, etc. Later feelings of disconnection, lethargy and inability to concentrate, tiredness, depression and confusion, and od...

Druginformer Identified Side Effects: Anger, Tinnitus

Posted By Anonymous in askapatient.com on July 15, 2007 @ 12:00 am

I finished taking this medicine 2 months ago, and have very loud ringing in my ears, it is driving me mad. I wouldnt recommend this medicine to anybody, its not worth the...

Druginformer Identified Side Effects: Fatigue, Abdominal pain, Night sweats, Tinnitus, Deafness, Dehydration, Diarrhoea, Dry mouth, Hyperhidrosis, Mouth ulceration, Decreased appetite

Posted By Anonymous in askapatient.com on July 14, 2007 @ 12:00 am

... cramping. I've also experienced ringing in my ears to the point of feeling like I'm going deaf and mouth ulcers. Night sweats, day sweats and feeling very tired despite getting adequate sleep. <...

Druginformer Identified Side Effects: Asthenia, Hypoaesthesia, Tinnitus, Anxiety, Electrolyte imbalance, Euphoric mood, Cardiac flutter, Abnormal dreams, Confusional state, Depression, Discomfort, Disorientation, Ear infection, Gait disturbance, Insomnia, Muscular weakness, Chapped lips, Haemorrhage, Decreased appetite, Vomiting projectile

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

Side Effects: Sickness and vomiting (projectile), no appetite, loss of balance, light headed, full feeling in head, ringing in the ears, anxiety (high), mild confusion, disorientation, depression, vi...

Druginformer Identified Side Effects: Tinnitus, Dyspepsia, Insomnia

Posted By Anonymous in askapatient.com on April 25, 2005 @ 12:00 am

Side Effects: Upset stomach and inability to sleep. Even after taking a Vicidin, I only slept for 2 hours. I wake up with ringing in my ears and I do not drink even caffiene. Probably worth...

* 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.