should you stop taking pain pills if having blood workdone

#Should you stop taking pain pills if having blood workdone how to
#Should you stop taking pain pills if having blood workdone update
#Should you stop taking pain pills if having blood workdone professional

Because we are constantly monitoring the safety of opioid pain medicines, we are also including new prescribing information on other side effects including central sleep apnea and drug interactions.

#Should you stop taking pain pills if having blood workdone update

We are continuing to monitor this safety concern and will update the public if we have new information.

#Should you stop taking pain pills if having blood workdone professional

Contact your health care professional if you experience increased pain, withdrawal symptoms, changes in your mood, or thoughts of suicide. Even when the opioid dose is decreased gradually, you may experience symptoms of withdrawal (See Additional Information for Patients).

#Should you stop taking pain pills if having blood workdone how to

Patients taking opioid pain medicines long-term should not suddenly stop taking your medicine without first discussing with your health care professional a plan for how to slowly decrease the dose of the opioid and continue to manage your pain. Create a patient-specific plan to gradually taper the dose of the opioid and ensure ongoing monitoring and support, as needed, to avoid serious withdrawal symptoms, worsening of the patient’s pain, or psychological distress (For tapering and additional recommendations, see Additional Information for Health Care Professionals). No standard opioid tapering schedule exists that is suitable for all patients.

When you and your patient have agreed to taper the dose of opioid analgesic, consider a variety of factors, including the dose of the drug, the duration of treatment, the type of pain being treated, and the physical and psychological attributes of the patient. Health care professionals should not abruptly discontinue opioids in a patient who is physically dependent. Examples of common opioids include codeine, fentanyl, hydrocodone, hydromorphone, morphine, oxycodone, and oxymorphone. They have serious risks, including abuse, addiction, overdose, and death. Opioids are a class of powerful prescription medicines that are used to manage pain when other treatments and medicines cannot be taken or are not able to provide enough pain relief. Patients may attempt to treat their pain or withdrawal symptoms with illicit opioids, such as heroin, and other substances. In turn, these symptoms can lead patients to seek other sources of opioid pain medicines, which may be confused with drug-seeking for abuse. Rapid discontinuation can result in uncontrolled pain or withdrawal symptoms. These changes will provide expanded guidance to health care professionals on how to safely decrease the dose in patients who are physically dependent on opioid pain medicines when the dose is to be decreased or the medicine is to be discontinued. While we continue to track this safety concern as part of our ongoing monitoring of risks associated with opioid pain medicines, we are requiring changes to the prescribing information for these medicines that are intended for use in the outpatient setting. These include serious withdrawal symptoms, uncontrolled pain, psychological distress, and suicide.

Food and Drug Administration (FDA) has received reports of serious harm in patients who are physically dependent on opioid pain medicines suddenly having these medicines discontinued or the dose rapidly decreased.