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See our list of 27 drugs you should never take with methotrexate. If you are currently taking celecoxib (CELEBREX)you should contact your physician to consider alternative NSAID treatment. In a recent complaint to the FDA, we took several makers of diabetes drugs to task for direct-to-consumer ads that promote the drugs for unapproved uses.

The Food and Drug Administration (FDA) now requires that the professional product labeling, or package inserts, for all fluroquinolone antibiotics must warn about the possibility of peripheral neuropathy (nerve damage). In this article, we highlight problems with these so-called abuse-deterrent opioid formulations. Read our independent analysis of the data considered by the FDA when it approved this new gout drug and our assessment of why you should not use it. Etanercept, an effective disease-modifying anti-rheumatic drug (DMARD), now joins adalimubab (HUMIRA) and inflixamib (REMICADE) to be the third of the arthritis disease-modifying drugs (see discussion on the following page about disease-modifying drugs) to receive a black box warning concerning infections, calling for TB testing and, if positive, TB treatment before starting these drugs. If this were true, it would be a clear example of the unintended consequences of regulation.



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Tc fanolesomab, a drug to help diagnose appendicitis, from the market because of potentially fatal adverse drug reactions, according to a Dec. Food and Drug Administration, recently warned physicians and patients about safety concerns regarding two drugs commonly used to treat Alzheimer’s disease. There is no evidence to suggest that aripiprazole is a “breakthrough” drug.

Numerous advertisements in magazines and on television and the Internet tout the miraculous age-reversing and bodybuilding properties of synthetic growth hormone treatment. Memantine (NAMENDA) recently has been one of the drugs for Alzheimer’s disease most heavily promoted through direct-to-consumer advertising. Find out why the most commonly prescribed drug of any kind in the U. Nothing could be simpler and more effective than a letter to doctors in addition to what the FDA has already agreed to do. Public Citizen researchers present safety and efficacy data about prasugrel hydrochloride, and recommend labeling to effectively communicate the drug's risks (including hemorrhage and cancer) to consumers.


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