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User Voices for Acetaminophen; Aspirin; Caffeine

The following are comments from users that experienced side effects while taking Acetaminophen; Aspirin; Caffeine

Back Pain

Side Effects: I woke up from a dead sleep with Intense back and stomach pain about 2 hours after use. Tightness in chest and dizziness. I felt very weird and very short of breath. I also felt very an...


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Did the author experience back pain while taking excedrin (migraine)?

What is this?

Back Pain

Side Effects: my migraines are cured but Severe side effect such as i am getting regular back pain after taking this EXCEDRIN (MIGRAINE)

please stop taking this medicine


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Did the author experience back pain while taking excedrin (migraine)?

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Back Pain

Side Effects: I took 2pills of excedrin (migraine) aroud 8pm and I was fine my migraine went away but like 2 hours later I started filling stomach and back pain and I was awake until 1:40am and then ...


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Did the author experience back pain while taking excedrin (migraine)?

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Back Pain

Side Effects: After taking the migraine pills last night(10:30P.m) . The headache was gone. Until this morning around 9:45 A.M. Back pains occurred, hard to breath, vomiting. Please email me ASAP, if...


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Did the author experience back pain while taking excedrin (migraine)?

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Back Pain

Side Effects: Backache & chest pain

Every time I take it I ususally lay down and take a short nap, I wake up with my headache gone but a very bad upper backache and chest pain near the cent...


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Did the author experience back pain while taking excedrin (migraine)?

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* 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.