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Acetaminophen, Aspirin And Caffeine

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* Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients.

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Druginformer Identified Side Effects: None

Posted By chinnajaggu in facebook.com on June 16, 2014 @ 12:00 am

June 16, 2014 · Migraine Headaches - Exams and Tests Your doctor will diagnose a migraine by examining you and asking questions about your health and lifestyle. There are no tests that can prove t...

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Posted By 100000158743875 in facebook.com on August 27, 2012 @ 12:00 am

The generic brands were not taken off the shelves. You could also just purchase the components separately and take them together - it is just acetaminophen, aspirin and caffeine.

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Posted By Verwon in prescriptiondrug-info.com on March 19, 2011 @ 12:00 am

If there were no markings on them, it is going to be difficult to determine exactly what they were. It is possible that they were a generic or store brand of Excedrin Migraine, which would conta...

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Posted By Verwon in prescriptiondrug-info.com on October 15, 2009 @ 12:00 am

That is correct, this is Extra Strength Excedrin, it contains Acetaminophen, Aspirin and Caffeine. This is a pain reliever and fever reducer. Is there anything else I can help you with?

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Posted By Verwon in prescriptiondrug-info.com on August 12, 2008 @ 12:00 am

It can be hard to get proper treatment for any type of pain from a lot of doctors, especially if the tests you have had so far do not show any problems and they have been giving you medications and yo...


* 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.