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Excedrin (migraine) Related Renal pain

Official Government Database Reports7
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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: Renal pain, Chest pain, Neck pain, Dizziness, Abdominal discomfort, Euphoric mood, Dyspnoea, Migraine, Psychomotor hyperactivity, Abasia, Poor quality sleep

Posted By Anonymous in askapatient.com on June 11, 2014 @ 12:00 am

... and light headed. Then came the chest and neck pains, which spread to my left arm. I kept waking up during the night and was extremely hyper. In the morning I had stomach and kidney pain that was so s...

Druginformer Identified Side Effects: Chest discomfort, Tremor, Renal pain, Feeling cold, Abdominal pain, Nausea, Abdominal discomfort, Chills, Feeling jittery, Burning sensation, Vomiting, Blepharospasm, Hypoaesthesia, Tinnitus, Accidental poisoning, Heart rate irregular, Hyperhidrosis, Vision blurred

Posted By Anonymous in askapatient.com on March 15, 2014 @ 12:00 am

... Drug from hell!! Fast heart beat , nausea, vomiting several times, abdominal pain , kidney pain, shakes , chills , jittery , ears ringing, eye twitches when closed , tight chest feeling, odd blurry vi...


* 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.