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Cardura Xl

Ingredients: Doxazosin Mesylate
Average User Review Score
* Based on 4 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: None

Posted By Anonymous in drugs.com on October 31, 2013 @ 12:00 am

Used Cardura XL on/off for several years now and more regularly recently. Wanted new prescription after moving to Europe, however doctor didn't now the product and recommended as alternative Tamsulosi...

Druginformer Identified Side Effects: None

Posted By Anonymous in druglib.com

Side Effects: None that I am aware of. Reduced prostate pain. I took this medication to reduce pain I was experiencing with my prostate. It took about two to three weeks after...

Druginformer Identified Side Effects: Loss of libido

Posted By Anonymous in druglib.com

Side Effects: None with Cardura. I switched from Flomax because the minimum dosage of 4 mg reduced libido and erectile strength. Not completely, but "half-mast" so to speak. Increased...

Druginformer Identified Side Effects: Loss of libido

Posted By Anonymous in druglib.com

Side Effects: None with Cardura. I switched from Flomax because the minimum dosage of 4 mg reduced libido and erectile strength. Not completely, but "half-mast" so to speak. Increased...

Druginformer Identified Side Effects: None

Posted By Verwon in prescriptiondrug-info.com on May 19, 2006 @ 12:00 am

Pill Image This is Doxazosin 8mgs, a generic for Cardura XL, this is used to lower high blood pressure.


* 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.