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Allegra-d 12 Hour

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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 crystal Melton in drugs.com on December 28, 2008 @ 12:00 am

Allegra-D 12 hour Need help. My daughter started taking Zyrtec-D when she was about 14 years old and I began to notice a change in her personality. She began to not be so happy anymore and started...

Druginformer Identified Side Effects: None

Posted By SoMuchToBeCleanFor in drugs.com on December 28, 2008 @ 12:00 am

I'm not too sure anyone on here will be able to help you. This forum mostly discusses other issues. Have you talked to your doctor? Is she still taking the Allegra? Have any huge life events occu...

Druginformer Identified Side Effects: None

Posted By lucy heflin in prescriptiondrug-info.com on January 21, 2008 @ 12:00 am

Can you cut an Allegra 12 hour extended release tablet in half? I took one the last 2 mornings and had trouble sleeping both nights.

Druginformer Identified Side Effects: None

Posted By Anonymous in prescriptiondrug-info.com on January 24, 2006 @ 12:00 am

fexofenadine HCI 160mg/p pseudoephedrine HCI 120mg

* 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.