FIBROVEIN 3% sodium tetradecyl sulfate 30mg/1mL multidose injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

fibrovein 3% sodium tetradecyl sulfate 30mg/1ml multidose injection vial

australasian medical & scientific ltd - sodium tetradecyl sulfate, quantity: 30 mg/ml - injection, solution - excipient ingredients: benzyl alcohol; water for injections; dibasic sodium phosphate dodecahydrate; monobasic potassium phosphate; sodium hydroxide - indications as at 09 june 2005 : the solution is designed for injection directly into the lumen of the varicose vein and is used as a sclerosant in the treatment of uncomplicated varicose veins of the leg by compression sclerotherapy. the strength of fibrovein selected depends on the size of the veins to be treated. fibrovein 3% is for the treatment of large superficial varicose veins. fibrovein 1% is for the treatment of small varicose veins and the larger venules. minor venules and spider veins (venous flares) should be treated with fibrovein 0.5% or 0.2%. the selection of the incorrect strength particularly in the case of minor venules and spider veins is liable to give rise to adverse reactions.

Brush, prophylaxis, teeth Australia - English - Department of Health (Therapeutic Goods Administration)

brush, prophylaxis, teeth

disposable medical supplies pty ltd - 35768 - brush, prophylaxis, teeth - to be uconnected to a dental handpiece and used by a dental hygienist and/or dentist to clean and polish teeth after treament.

EPIPEN Israel - English - Ministry of Health

epipen

trupharm marketing 1985 ltd. - epinephrine - solution for injection - epinephrine 1 mg / 1 ml - epinephrine - epinephrine - epipen is indicated in the emergency treatment of severe allergic reactions (type i) including anaphylaxis to stinging insects (e.g., order hymenoptera, which include bees, wasps, hornets, yellow jackets and fire ants) and biting insects (e.g., triatoma, mosquitoes), allergen immunotherapy, foods, drugs, diagnostic testing substances (e.g., radiocontrast media) and other allergens, as well as idiopathic anaphylaxis or exercise-induced anaphylaxis.epipen is intended for immediate administration in patients who are determined to be at increased risk for anaphylaxis, including individuals with a history of anaphylactic reactions. epipen is intended for immediate administration as emergency supportive therapy only and is not a substitute for immediate medical care.

EPIPEN JR Israel - English - Ministry of Health

epipen jr

trupharm marketing 1985 ltd. - epinephrine - solution for injection - epinephrine 0.5 mg / 1 ml - epinephrine - epinephrine - epipen jr is indicated in the emergency treatment of severe allergic reactions (type i) including anaphylaxis to stinging insects (e.g., order hymenoptera, which include bees, wasps, hornets, yellow jackets and fire ants) and biting insects (e.g., triatoma, mosquitoes), allergen immunotherapy, foods, drugs, diagnostic testing substances (e.g., radiocontrast media) and other allergens, as well as idiopathic anaphylaxis or exercise-induced anaphylaxis.epipen jr is intended for immediate administration in patients who are determined to be at increased risk for anaphylaxis, including individuals with a history of anaphylactic reactions. epipen jr is intended for immediate administration as emergency supportive therapy only and is not a substitute for immediate medical care.

Trolley, medical devices Australia - English - Department of Health (Therapeutic Goods Administration)

trolley, medical devices

ems oceania pty ltd - 40596 - trolley, medical devices - to be used to support / transport various medical device systems and provide utilities where needed such as bottled water supply and storage space.

Adrenaline (base) for anaphylaxis 1mg/1ml (1 in 1,000) solution for injection pre-filled syringes United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

adrenaline (base) for anaphylaxis 1mg/1ml (1 in 1,000) solution for injection pre-filled syringes

base) for anaphylaxis 1mg/1ml (1 in 1,000) solution for injection pre-filled syringes (martindale pharmaceuticals ltd - adrenaline - solution for injection - 1mg/1ml

CEFUROXIME SXP cefuroxime (as sodium) 1500 mg powder for  injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

cefuroxime sxp cefuroxime (as sodium) 1500 mg powder for injection vial

southern xp ip pty ltd - cefuroxime sodium, quantity: 1577.7 mg (equivalent: cefuroxime, qty 1500 mg) - injection, powder for - excipient ingredients: - cefuroxime sxp is indicated in adults and children of 40 kg or greater in weight for the prevention of infections associated with certain surgical procedures of the gastrointestinal (including oesophageal), orthopaedic, cardiovascular and gynaecological systems (including caesarean section) (see section 4.4: special warnings and precautions for use and section 5.2: pharmacokinetic properties).,in the prevention of infections in which it is very likely that anaerobic organisms will be encountered, cefuroxime should be administered with additional appropriate antibacterial agents such as metronidazole.,consideration should be given to official guidance on the appropriate use of antibacterial agents, as antibiotic prophylaxis is not required in all gastrointestinal, orthopaedic, cardiovascular and gynaecological procedures or surgeries.,for patients with specific cardiac conditions which predispose them to endocarditis who are undergoing abdominal surgery for which surgical antibiotic prophylaxis is indicated, the prophylaxis regimen should additionally include an antibiotic active against enterococci.,for patients undergoing orthopedic or cardiovascular surgery known to be, or at risk of being, colonised or infected with methicillin-resistant s. aureus (mrsa), add an antibiotic with activity against mrsa, such as vancomycin.,cefuroxime sxp is not indicated in children less than 40 kg in weight.

CEFUROXIME SXP cefuroxime (as sodium) 750 mg powder for  injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

cefuroxime sxp cefuroxime (as sodium) 750 mg powder for injection vial

southern xp ip pty ltd - cefuroxime sodium, quantity: 788.9 mg (equivalent: cefuroxime, qty 750 mg) - injection, powder for - excipient ingredients: - cefuroxime sxp is indicated in adults and children of 40 kg or greater in weight for the prevention of infections associated with certain surgical procedures of the gastrointestinal (including oesophageal), orthopaedic, cardiovascular and gynaecological systems (including caesarean section) (see section 4.4: special warnings and precautions for use and section 5.2: pharmacokinetic properties).,in the prevention of infections in which it is very likely that anaerobic organisms will be encountered, cefuroxime should be administered with additional appropriate antibacterial agents such as metronidazole.,consideration should be given to official guidance on the appropriate use of antibacterial agents, as antibiotic prophylaxis is not required in all gastrointestinal, orthopaedic, cardiovascular and gynaecological procedures or surgeries.,for patients with specific cardiac conditions which predispose them to endocarditis who are undergoing abdominal surgery for which surgical antibiotic prophylaxis is indicated, the prophylaxis regimen should additionally include an antibiotic active against enterococci.,for patients undergoing orthopedic or cardiovascular surgery known to be, or at risk of being, colonised or infected with methicillin-resistant s. aureus (mrsa), add an antibiotic with activity against mrsa, such as vancomycin.,cefuroxime sxp is not indicated in children less than 40 kg in weight.

Ibuprofen Chanelle Medical 200 mg capsules, soft Ireland - English - HPRA (Health Products Regulatory Authority)

ibuprofen chanelle medical 200 mg capsules, soft

chanelle medical - ibuprofen lysine - capsule, soft - 200 milligram(s) - propionic acid derivatives; ibuprofen