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Get the free ( and naloxone) sublingual film. Approval Letter - samhsa - buprenorphine samhsa

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DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration Silver Spring MD 20993 NDA 022410 NDA APPROVAL Reckitt Benckiser Pharmaceuticals Inc. 10710 Midlothian Turnpike, Suite 430 Richmond,
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How to fill out and naloxone sublingual film:

01
Open the package of naloxone sublingual film carefully.
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Make sure your hands are clean and dry before handling the film.
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Take out one film from the package and hold it using clean fingertips.
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Place the film under your tongue, close to the base.
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Allow the film to dissolve completely without chewing or swallowing it.
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Do not eat or drink for at least 30 minutes after taking the naloxone sublingual film.
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Dispose of the packaging and any remaining unused films properly.

Who needs naloxone sublingual film:

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Naloxone sublingual film is commonly used for the emergency treatment of opioid overdose.
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It is especially important for individuals who are at risk of overdose or may witness an overdose event to have naloxone available.
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People who use opioids recreationally or are on opioid-based medications, such as for pain management, may benefit from having naloxone sublingual film on hand.
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Healthcare providers, first responders, and those who work in settings where opioid overdose is a concern should also consider having naloxone available.
Note: It is important to consult with a healthcare professional for proper usage and to determine if naloxone sublingual film is appropriate for your specific needs.
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Naloxone sublingual film is a medication used to rapidly reverse opioid overdose.
Healthcare providers and pharmacies are required to file naloxone sublingual film.
Naloxone sublingual film should be filled out with patient information, dosage administered, and the date and time of administration.
The purpose of naloxone sublingual film is to quickly reverse the effects of opioid overdose and restore normal breathing.
Information such as patient name, dosage administered, date and time of administration, and the name of the healthcare provider or pharmacy should be reported on the naloxone sublingual film.
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