DrugInformer Search

Allegra d 24 hour Related Dry mouth

Official Government Database Reports16
Online Conversations4

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 Allegra D 24 Hour

Thank you for sharing your experience with us!

Share Your Experience

Druginformer Identified Side Effects: Nausea, Lethargy, Acne, Dehydration, Disturbance in attention, Dry mouth, Insomnia, Decreased appetite

Posted By Anonymous in askapatient.com on September 20, 2011 @ 12:00 am

Side Effects: insomnia, loss of appetite, some dry mouth/dehydration, feel little nauseous/lethargic for a short bit right after taking. Been taking for 2 or 3 years and it sorta takes the ...

Druginformer Identified Side Effects: Dry mouth, Somnolence

Posted By Anonymous in askapatient.com on May 15, 2011 @ 12:00 am

Side Effects: Drowsiness. Dry mouth. I have no official complaints about Allegra D. I was taking it when you still need a prescription and the only problem I had was that the pill was giant...

Druginformer Identified Side Effects: Lethargy, Dehydration, Disturbance in attention, Dry mouth, Insomnia, Decreased appetite

Posted By Anonymous in askapatient.com on April 25, 2011 @ 12:00 am

... enough to be sure), feeling of dehydration in general (my skin is extra dry, my nose gets really crusty (sorry its gross, but true), feeling kinda "drugged" (like a little out of it, but not too sever...

Druginformer Identified Side Effects: Dysuria, Heart rate, Dry mouth, Hyperhidrosis

Posted By Anonymous in askapatient.com on July 10, 2010 @ 12:00 am

Side Effects: Difficulty urinating, dry mouth, inreased heart rate, excessive sweating. Didn't do too much for my allergies and side-effects outweighted benefits so I am tapering off this m...

* 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.