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Atacand Hct

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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 Verwon in prescriptiondrug-info.com on January 6, 2011 @ 12:00 am

Vim-25 is a natural supplement that is claimed to help with erectile dysfunction. Being a natural product, that is not actually proven to do anything, the side effect or interaction profiles hav...

Druginformer Identified Side Effects: None

Posted By Anonymous in drugs.com on January 19, 2005 @ 12:00 am

322/A CJ is a Candesartan Cilexetil 32mg, Hydrochlorothiazide 12.5mg tablet, brand name Atacand HCT Yellow oval tablet Imprint A CJ/ 322 Drug info available at http://www.drugs.com/cdi/ataca...

Druginformer Identified Side Effects: None

Posted By Dixiefireball in ic-network.com on February 26, 2004 @ 12:00 am

Free and Low Cost Prescription Drugs ... n some cases, households with incomes as high as $50,000 ... LEVELS ,NOT QUALIFIED FOR MEDICAID ,UP TO $50,000 INCOME. ... Free and Low Cost Medical Care Ope...

Druginformer Identified Side Effects: None

Posted By Salwa in facebook.com

WHAT ARE THE SPECIFIC DRUG TREATMENTS USED FOR HIGH BLOOD PRESSURE? There are several classes of drugs used to treat hypertension. Diuretics Benefits of Diuretics. Some of the benefits reported on d...

* 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.