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

echo therapeutics pty ltd - buprenorphine hydrochloride, quantity: 324 microgram/ml (equivalent: buprenorphine, qty 300 microgram/ml) - injection, solution - excipient ingredients: glucose monohydrate; hydrochloric acid; water for injections - temgesic injection is indicated for the short-term (not more than one week) management of severe pain for which other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain. temgesic injection should be employed when sublingual administration is not practical e.g. pre- or peri-operatively. temgesic is not recommended for use in children. temgesic does not have an approved role in opioid dependence rehabilitation programmes.

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

pharmaco australia ltd - midazolam, quantity: 5 mg/ml - injection, solution - excipient ingredients: hydrochloric acid; sodium chloride; water for injections; sodium hydroxide - 1. intravenously as an agent for conscious sedation prior to short surgical, diagnostic, therapeutic or endoscopic procedures, such as bronchoscopy, gastroscopy, cystoscopy, coronary angiography and cardiac cathetherization, either alone or in conjunction with a narcotic; 2. intravenously for induction of anaesthesia, preliminary to administration of other anaesthetic agents. with the use of a narcotic premedicant, induction of anaesthesia can be attained with narrower dose range and in a shorter period of time; 3. sedation in intensive care units by intravenous intermittent administration or continuous infusion; 4. intramuscularly for preoperative sedation (induction of sleepiness or drowsiness and relief of apprehension) and to impair memory of perioperative events.

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

novartis pharmaceuticals australia pty ltd - ciclosporin, quantity: 50 mg/ml - injection, concentrated - excipient ingredients: ethanol; peg-35 castor oil - this product is accepted for registration as 'currently supplied' at the time of commencement of the act. new indications were approved as specified in the letter of 16 june 1992 from dr l. hunt. indications: as an immunosuppressive agent for the prevention of graft rejection following kidney, liver and heart allogeneic transplantation. extended indications as at 15 october 1993: for induction and/or maintenance of remission in the nephrotic syndrome. cyclosporin is not a first-line agent. its use should be restricted to occasions when steroids and cytostatic drugs have failed, or are not tolerated, or are considered inappropriate, and when renal function is unimpaired . indications as at 11 february 1994 from dr j. mcginness: 1. as an immunosuppressive agent for the prevention of graft rejection following kidney, liver and heart allogeneic transplantation. 2. for induction and/or maintenance of remission in the nephrotic syndrome. cyclosporin is not a first-line agent. its use should be restricted to occas

Jordania - inglés - JFDA (Jordan Food & Drug Administration - المؤسسة العامة للغذاء والدواء)

شركة مستودع الأدوية الأردني - the jordan drugstore co - methylergometrine maleate 0.2 mg/ml - 0.2 mg/ml

Irlanda - inglés - HPRA (Health Products Regulatory Authority)

anaquest limited - halothane - 250 milligram

Irlanda - inglés - HPRA (Health Products Regulatory Authority)

concord pharmaceuticals ltd - halothane - 0.01 %w/w

India - inglés - Central Drugs Standard Control Organization

raman & weil - halothane - 30/50;ml

Australia - inglés - APVMA (Australian Pesticides and Veterinary Medicines Authority)

merial australia pty ltd - halothane - anaesthetics/analgesics - animal | birds | calf | cattle | horse | horse foal | pig - heavier than 30 kg liveweight | pig - less than 30 kg liveweight | r - anaesthetic - local/general | general anaesthetic | immobiliser | local anaesthetic | premedication | sedative | tranquilliser | travel sickness

Irlanda - inglés - HPRA (Health Products Regulatory Authority)

eurovet animal health b.v. - ketamine hydrochloride - solution for injection - 100 milligram(s)/millilitre - ketamine - cats, dogs, horses - neurological preparations

Reino Unido - inglés - HMA (Heads of Medicines Agencies)

le vet b.v - detomidine hydrochloride 10 mg/ml - solution for injection - horses food, pigs food - other hypnotics and sedatives