Pressure bandage, non-latex, non-sterile, reusable Australia - English - Department of Health (Therapeutic Goods Administration)

pressure bandage, non-latex, non-sterile, reusable

bsn medical (aust) pty ltd - 61223 - pressure bandage, non-latex, non-sterile, reusable - to be applied to and compress a local area of the body for one or more preventative/therapeutic applications (e.g. treatment of lymphoedema, venous oedema and lipoedema, and other phlebological indications).

Compression/pressure tubular garment Australia - English - Department of Health (Therapeutic Goods Administration)

compression/pressure tubular garment

bsn medical (aust) pty ltd - 64438 - compression/pressure tubular garment - to tightly fit over and apply compression/pressure (i.e., graduated or even-force) to a part of a limb, typically for the treatment/prevention of a disorder(s) of circulation [e.g., venous insufficiency, deep vein thrombosis (dvt)], to control scarring, and/or to manage lymphoedema.

NA- lidocaine hydrochloride injection, solution United States - English - NLM (National Library of Medicine)

na- lidocaine hydrochloride injection, solution

sintetica us llc - lidocaine hydrochloride anhydrous (unii: ec2cnf7xfp) (lidocaine - unii:98pi200987) - lidocaine is contraindicated in patients with a known history of hypersensitivity to local anesthetics of the amide type.

NA- lidocaine hydrochloride injection, solution United States - English - NLM (National Library of Medicine)

na- lidocaine hydrochloride injection, solution

sintetica us llc - lidocaine hydrochloride anhydrous (unii: ec2cnf7xfp) (lidocaine - unii:98pi200987) - lidocaine hydrochloride injection is indicated for production of local or regional anesthesia by infiltration techniques such as percutaneous injection, by peripheral nerve block techniques such as brachial plexus and intercostal and by central neural techniques such as lumbar and caudal epidural blocks, when the accepted procedures for these techniques as described in standard textbooks are observed. lidocaine hcl is contraindicated in patients with a known history of hypersensitivity to local anesthetics of the amide type.

Cast removal protective tape Australia - English - Department of Health (Therapeutic Goods Administration)

cast removal protective tape

bsn medical (aust) pty ltd - 66583 - cast removal protective tape - to be placed between a cast stockinette and the lining of a cast, along the line where subsequent cast cutting is intended to occur during cast removal, to prevent cuts and burns to the skin caused by the cast cutter/saw.

KETOROLAC TROMETHAMINE tablet, film coated United States - English - NLM (National Library of Medicine)

ketorolac tromethamine tablet, film coated

leading pharma, llc - ketorolac tromethamine (unii: 4eve5946bq) (ketorolac - unii:yzi5105v0l) - carefully consider the potential benefits and risks of ketorolac tromethamine tablets and other treatment options before deciding to use ketorolac tromethamine tablets. use the lowest effective dose for the shortest duration consistent with individual patient treatment goals. acute pain in adult patients ketorolac tromethamine tablets are indicated for the short-term (≤5 days) management of moderately severe acute pain that requires analgesia at the opioid level, usually in a postoperative setting. therapy should always be initiated with iv or im dosing of ketorolac tromethamine and ketorolac tromethamine tablets are to be used only as continuation treatment, if necessary. the total combined duration of use of ketorolac tromethamine tablets and ketorolac tromethamine is not to exceed 5 days of use because of the potential of increasing the frequency and severity of adverse reactions associated with the recommended doses (see warnings, precautions, dosage and administration, andadverse reactions ). patients should be switched to alternative analgesics as soon as possible, but ketorolac tromethamine tablet therapy is not to exceed 5 days. ketorolac tromethamine is contraindicated in patients with previously demonstrated hypersensitivity to ketorolac tromethamine. ketorolac tromethamine is contraindicated in patients with active peptic ulcer disease, in patients with recent gastrointestinal bleeding or perforation and in patients with a history of peptic ulcer disease or gastrointestinal bleeding. ketorolac tromethamine should not be given to patients who have experienced asthma, urticaria, or allergic-type reactions after taking aspirin or other nsaids. severe, rarely fatal, anaphylactic-like reactions to nsaids have been reported in such patients (see warnings, anaphylactoid reactions, and precautions, preexisting asthma ). ketorolac tromethamine is contraindicated as prophylactic analgesic before any major surgery. ketorolac tromethamine is contraindicated in the setting of coronary artery bypass graft (cabg) surgery (see warnings ). ketorolac tromethamine is contraindicated in patients with advanced renal impairment or in patients at risk for renal failure due to volume depletion (see warnings for correction of volume depletion). ketorolac tromethamine is contraindicated in labor and delivery because, through its prostaglandin synthesis inhibitory effect, it may adversely affect fetal circulation and inhibit uterine contractions, thus increasing the risk of uterine hemorrhage. ketorolac tromethamine inhibits platelet function and is, therefore, contraindicated in patients with suspected or confirmed cerebrovascular bleeding, hemorrhagic diathesis, incomplete hemostasis and those at high risk of bleeding (see warnings and precautions ). ketorolac tromethamine is contraindicated in patients currently receiving aspirin or nsaids because of the cumulative risks of inducing serious nsaid-related adverse events. the concomitant use of ketorolac tromethamine and probenecid is contraindicated. the concomitant use of ketorolac tromethamine and pentoxifylline is contraindicated.