DrugInformer Search

User Voices for Acetaminophen; Aspirin; Caffeine

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

Psychotic Disorder

Side Effects: Awful stomach pains and weird mental state.

Stay away from this. Read the reviews. I took it and it made my migraine go away, but I feel extremely nauseas along with stomach p...


Source: viewrating.asp

View full report on related psychotic disorder

Did the author experience psychotic disorder while taking excedrin (migraine)?

What is this?

Psychotic Disorder

Side Effects: Vertigo, diarrhea, anxiety, burning fiery pain through jaw and temple, inability to function due to mental confusion, fatigue-lethargy, blood in stool, lack of emotional control and the...


Source: viewrating.asp

View full report on related psychotic disorder

Did the author experience psychotic disorder while taking excedrin (migraine)?

What is this?

Psychotic Disorder

Side Effects: This is the worst feeling I ever had. I usually don't take pain killers, but have to when I get migraines (every 6-8 weeks). This is the first time I took two pills at once as recommend...


Source: viewrating.asp

View full report on related psychotic disorder

Did the author experience psychotic disorder while taking excedrin (migraine)?

What is this?

* 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.