| Subject: | FDA Warns of Injection Site Reactions With Naltrexone Injection |
| Category: | Food and Drug Administration (FDA)
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| Published: | Wed, 13 Aug 2008 - 11:00 am |
| The Food and Drug Administration (FDA) is informing healthcare professionals of the risk of adverse injection site reactions in patients receiving naltrexone (Vivitrol). Naltrexone is indicated for the treatment of alcohol dependence in patients who are able to abstain from alcohol in an outpatient setting prior to initiation of treatment. Naltrexone is administered as an intramuscular gluteal injection and should not be administered intravenously, subcutaneously, or inadvertently into fatty... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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