"The U.S. Food and Drug Administration today approved Hysingla ER (hydrocodone bitartrate), an extended-release (ER) opioid analgesic to treat pain severe enough to require daily, around-the-clock, long-term opioid treatment and for which alternat"...
Contains sodium metabisulfite, a sulfite that may cause allergic-type reactions including anaphylactic symptoms and life-threatening or less severe asthmatic episodes in certain susceptible people. The overall prevalence of sulfite sensitivity in the general population is unknown and probably low. Sulfite sensitivity is seen more frequently in asthmatic than in nonasthmatic people.
Oxycodone can produce drug dependence of the morphine type and, therefore, has the potential for being abused. Psychic dependence, physical dependence and tolerance may develop upon repeated administration of TYLOX (oxycodone and acetaminophen capsules) (oxycodone and acetaminophen capsules), and it should be prescribed and administered with the same degree of caution appropriate to the use of other oral narcotic-containing medications. Like other narcotic-containing medications, TYLOX (oxycodone and acetaminophen capsules) is subject to the Federal Control Substances Act (Schedule II).
Head Injury and Increased Intracranial Pressure: The respiratory depressant effects of narcotics and their capacity to elevate cerebrospinal fluid pressure may be markedly exaggerated in the presence of head injury, other intracranial lesions or a pre-existing increase in intracranial pressure. Furthermore, narcotics produce adverse reactions which may obscure the clinical course of patients with head injuries.
Acute Abdominal Conditions: The administration of TYLOX (oxycodone and acetaminophen capsules) (oxycodone and acetaminophen capsules) or other narcotics may obscure the diagnosis or clinical course in patients with acute abdominal conditions.
Special Risk Patients: TYLOX (oxycodone and acetaminophen capsules) should be given with caution to certain patients such as the elderly or debilitated, and those with severe impairment of hepatic or renal function, hypothyroidism, Addison's disease, and prostatic hypertrophy or urethral stricture.
Usage in Pregnancy
Pregnancy Category C. Animal reproductive studies have not been conducted with TYLOX (oxycodone and acetaminophen capsules) . It is also not known whether TYLOX (oxycodone and acetaminophen capsules) can cause fetal harm when administered to a pregnant woman or can affect reproductive capacity. TYLOX (oxycodone and acetaminophen capsules) should not be given to a pregnant woman unless in the judgment of the physician, the potential benefits outweigh the possible hazards.
Nonteratogenic Effects: Use of narcotics during pregnancy may produce physical dependence in the neonate.
Labor and Delivery
As with all narcotics, administration of TYLOX (oxycodone and acetaminophen capsules) to the mother shortly before delivery may result in some degree of respiratory depression in the newborn and the mother, especially if higher doses are used.
It is not known whether the components of TYLOX (oxycodone and acetaminophen capsules) are excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when TYLOX (oxycodone and acetaminophen capsules) is administered to a nursing woman.
Safety and effectiveness in children have not been established.
Last reviewed on RxList: 4/3/2009
This monograph has been modified to include the generic and brand name in many instances.
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