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Allegra D 24 Hour

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* Based on 15 reviews from across the web.
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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: Insomnia, Restlessness, Sleep disorder, Palpitations, Anxiety, Dry eye

Posted By Anonymous in askapatient.com on April 2, 2011 @ 12:00 am

Side Effects: insomnia, dry eyes, heart palpatations, anxiety generally have no problem sleeping, but when I took this drug I was up all night but still tired and could not calm down and go...

Druginformer Identified Side Effects: Hypersensitivity

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

Side Effects: No noticable side affects. Allergies cleared up after about a week while taking with Fluticasone Nasal Spray.

Druginformer Identified Side Effects: None

Posted By Anonymous in askapatient.com on February 5, 2011 @ 12:00 am

Side Effects: Allergra D changed my menstrual cycles. My periods were only 2-3 days long for most of my adult life. I was in my late 30's when I started taking it. I thought I might be in perimenapau...

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...

Druginformer Identified Side Effects: Headache, Fatigue, Withdrawal syndrome

Posted By Anonymous in askapatient.com on June 16, 2010 @ 12:00 am

Side Effects: only side effect is if i dont take it! then i go through a withdrawal like not having coffee...tired, headache...etc...but I can get through it using the 12 hour just once then veramyst...

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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.