Filipinas - inglés - FDA (Food And Drug Administration)

oxford distributions incorporated - choline salicylate , benzalkonium chloride - gel - 0.9g/ 0.002g

Filipinas - inglés - FDA (Food And Drug Administration)

oxford distributions, incorporated - phenylpropanolamine hydrochloride , paracetamol - syrup - 250 mg/12.5 mg

Filipinas - inglés - FDA (Food And Drug Administration)

oxford distributions incorporated - phenylpropanolamine hydrochloride - syrup (oral drops) - 6.25 mg/ml

Estados Unidos - inglés - NLM (National Library of Medicine)

oxford pharmaceuticals, llc - primidone (unii: 13afd7670q) (primidone - unii:13afd7670q) - primidone, used alone or concomitantly with other anticonvulsants, is indicated in the control of grand mal, psychomotor, and focal epileptic seizures. it may control grand mal seizures refractory to other anticonvulsant therapy. primidone is contraindicated in: 1) patients with porphyria and 2) patients who are hypersensitive to phenobarbital (see actions ).

Estados Unidos - inglés - NLM (National Library of Medicine)

oxford pharmaceuticals, llc - paroxetine hydrochloride (unii: x2els050d8) (paroxetine - unii:41vrh5220h) - paroxetine is indicated in adults for the treatment of: - major depressive disorder (mdd) - obsessive compulsive disorder (ocd) - panic disorder (pd) - social anxiety disorder (sad) - generalized anxiety disorder (gad) - posttraumatic stress disorder (ptsd) paroxetine is contraindicated in patients: - taking, or within 14 days of stopping, maois (including the maois linezolid and intravenous methylene blue) because of an increased risk of serotonin syndrome [see warnings and precautions (5.2), drug interactions ( 7)]. - taking thioridazine because of risk of qt prolongation [see warnings and precautions (5.3) and drug interactions (7)]. - t aking pimozide because of risk of qt prolongation[see warnings and precautions (5.3), drug interactions (7)]. - with known hypersensitivity (e.g., anaphylaxis, angioedema, stevens-johnson syndrome) to paroxetine or any of the inactive ingredients in paroxetine tablets, usp[see adverse reactions (6.1), (6.2)] . pregnancy category d [see warnings and precautions (5.4)]

Australia - inglés - Department of Health (Therapeutic Goods Administration)

zimmer biomet pty ltd - 34195 - unicondylar knee prosthesis - a partial knee system to be used in patients with anteromedial osteoarthritis or avascular necrosis. the device consists of a spherical design femoral bearing surface with a fully mobile bearing that stays congruent with the femoral component throughout the entire range of motion. the tibial tray is anatomically shaped and has a highly polished surface for the bearing to articulate on. the bearing is intended to be imlanted without the use of bone cement. the cementless oxford partial knee is intended for use in individuals with osteoarthritis or avascular necorosis limited to the medial compartment of the knee and is intended to be implanted without the application of bone cement.

Australia - inglés - Department of Health (Therapeutic Goods Administration)

zimmer biomet pty ltd - 34195 - unicondylar knee prosthesis - the tibial component of a partial knee. the tray is anatomically shaped and has a highly polished surface for the bearing to articulate on. the keel is modified to include an extractor slot the oxford partial knee is intended for use in individuals with osteoarthritis or avascular necrosis limited to the medial compartment of the knee and is intended to be implanted with bone cement.

Australia - inglés - Department of Health (Therapeutic Goods Administration)

zimmer biomet pty ltd - 34195 - unicondylar knee prosthesis - the bearings are manufactured from direct compression uhmwpe. the bearings have radii of curvature to match the femoral components. the oxford partial knee is intended for use in individuals with osteoarthritis or avascular necrosis limited to the medial compartment of the knee and is intended to be implanted with bone cement.

Australia - inglés - Department of Health (Therapeutic Goods Administration)

zimmer biomet pty ltd - 34195 - unicondylar knee prosthesis - a partial knee cemented tibial tray designed to be used in the lateral knee compartment. the tray has a domed top that is fully congruent with a matching bioconcaved bearing. this assists in resisting lateral dislocation during flexion and allows for deep flexion without impingement. biomet uk ltd. knee joint replacement prostheses provide the surgeon with a means of reducing pain and restoring function for many patients. whilst these devices are generally successful in attaining these goals they cannot be expected to withstand the activity levels and loads of normal healthy bone. the indications for use of the joint replacement prostheses include: 1)osteoarthritis, rheumatoid arthritis or traumatic arthritis 2)failure of a previous joint replacement procedure 3)correction of varus, valgus or post-traumatic deformity 4)correction or revision of unsuccessful osteotomy or arthrodesis. specifically for oxford lateral prostheses 1) isolated lateral compartment os or lateral avn 2) correctable valgus deformi

Australia - inglés - Department of Health (Therapeutic Goods Administration)

zimmer biomet pty ltd - 34195 - unicondylar knee prosthesis - a partial knee system to be used in patients with anteromedial osteoarthritis or avascular necrosis. the device consists of a spherical design femoral bearing surface with a fully mobile bearing that stays congruent with the femoral component throughout the entire range of motion. the femoral component has a porous coating overlaid with hydroxyapatite. it is intended to be used uncemented the cementless oxford partial knee is intended for use in individuals with osteoarthritis or avascular necrosis limited to the medial compartment of the knee and is intended to be implanted without the application of bone cement.