Ten Drugs Make New FDA Watch List

April 03, 2017

Ten drugs or drug classes treating everything from obesity to arthritis made the latest watch list of drugs with possible safety issues that was released by the US Food and Drug Administration (FDA) last week.

The list reflects potential signals of serious risk or new safety information collected by the FDA Adverse Event Reporting System (FAERS) in the fourth quarter of 2016.

The combination of naltrexone and bupropion (Contrave, Orexigen Therapeutics) for weight loss was flagged because the FDA received reports that some patients were losing consciousness. Likewise, the agency detected a possible signal of diarrhea, vomiting, and nausea for the arthritis drug apremilast (Otezla, Celgene).

The FDA cautions that a drug's appearance on a quarterly FAERS watch list does not mean the agency has established a causal relationship with the cited adverse event. Instead, the agency is studying the need for regulatory action. If the FDA concludes that there is a causal link, it can collect more information to better describe the threat, revise the drug's label, order a risk evaluation and mitigation strategy, or withdraw the drug from the market.

Sometimes the FDA already has put the matter of a drug's potential risk signal to rest before it publishes the watch list. This kind of regulatory resolution was true for the diabetes drug glyburide (Diabeta, Sanofi-Aventis) in the fourth quarter list for 2016. The agency has updated the adverse-events section of the drug's label to include bullous reactions, erythema multiforme, and exfoliative dermatitis. Another example is ibrutinib (Imbruvica, Pharmacyclics and Janssen), indicated for chronic lymphocytic leukemia/small lymphocytic lymphoma, and two other types of lymphoma. The label was updated to warn about the risk for Pneumocystis jirovecii pneumonia.

                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                       
Product Name: Trade (Active Ingredient) or Product Class Potential Signal of a Serious Risk / New Safety Information Additional Information
           (as of March 31, 2017)
Contrave (naltrexone HCl and bupropion HCl) extended-release tabletsLoss of consciousnessFDA is evaluating the need for regulatory action.
Coumadin (warfarin sodium) tablets, for oral use
           Eliquis (apixaban) tablets, for oral use
           Pradaxa (dabigatran etexilate mesylate) caps
           Savaysa (edoxaban tosylate) tablets, for oral use
           Xarelto (rivaroxaban) tablets, for oral use
MenorrhagiaFDA decided that no action is necessary at this time based on available information.
Depo-Medrol (methylprednisolone acetate) injectable suspension, USP, not for use in neonates, contains benzyl alcohol intravenous use
           Depo-Provera (medroxyprogesterone acetate), injectable suspension, USP
           Depo-Provera CI (medroxyprogesterone acetate), injectable suspension, for intramuscular use
Medication errorsThe carton and container labeling was revised to help differentiate between Depo-Medrol and Depo-Provera products.
           Depo-Provera labeling
Diabeta (glyburide) tablets, USPSkin reactionsThe Adverse Reactions section of the labeling for Diabeta was updated to include bullous reactions, erythema multiforme, and exfoliative dermatitis.
           Diabeta labeling
Imbruvica (ibrutinib), capsules, for oral use Pneumocystis jirovecii pneumonia (PJP)The Warnings and Precautions section of the labeling for Imbruvica was updated to include PJP.
           Imbruvica labeling
Nitropress (sodium nitroprusside) injectionCarboxyhemoglobinemiaFDA is evaluating the need for regulatory action.
Northera (droxidopa) capsules, for oral useCerebrovascular accidentThe Warnings and Precautions section of the labeling for Northera was updated to include information about stroke.   The Adverse Reactions section of the labeling for Northera was updated with information about cerebrovascular accident.
           Northera labeling
           FDA is evaluating the need for other regulatory action.
Nucala (mepolizumab) for injection, for subcutaneous useAnaphylaxisThe Warning and Precautions section of the labeling for Nucala was updated to include anaphylaxis.
           Nucala labeling
Opsumit (macitentan) tablets, for oral useFluid overloadThe Warnings and Precautions section of the labeling for Opsumit was updated to include information about fluid retention.
           Opsumit labeling
Otezla (apremilast) tablets, for oral useDiarrhea, nausea, and vomitingFDA is evaluating the need for regulatory action.
           

Source: FDA

           

 

Follow Robert Lowes on Twitter @LowesRobert

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