United States -
English -
NLM (National Library of Medicine)
diclofenac sodium gel
hi-tech pharmacal co., inc. - diclofenac sodium (unii: qtg126297q) (diclofenac - unii:144o8ql0l1) - diclofenac sodium topical gel is indicated for the relief of the pain of osteoarthritis of joints amenable to topical treatment, such as the knees and those of the hands. diclofenac sodium topical gel is contraindicated in the following patients: pregnancy category c prior to 30 weeks gestation; category d starting 30 weeks gestation risk summary use of nsaids, including diclofenac sodium topical gel, during the third trimester of pregnancy increases the risk of premature closure of the fetal ductus arteriosus. avoid use of nsaids, including diclofenac sodium topical gel, in pregnant women starting at 30 weeks of gestation (third trimester). there are no adequate and well-controlled studies of diclofenac sodium topical gel in pregnant women. human and animal studies indicate that diclofenac crosses the placenta. data from observational studies regarding potential embryofetal risks of nsaid use in women in the first or second trimesters of pregnancy are inconclusive. in the general u.s. population, all clinica
United States -
English -
NLM (National Library of Medicine)
paregoric liquid
hi-tech pharmacal co., inc. - morphine (unii: 76i7g6d29c) (morphine - unii:76i7g6d29c) - morphine 2 mg in 5 ml - paregoric is useful for the treatment of diarrhea. hypersensitivity to morphine. because of its stimulating effect on the spinal cord, morphine should not be used in convulsive states, such as those occurring in status epilepticus, tetanus, and strychnine poisoning. this preparation should not be used in diarrhea caused by poisoning until the toxic material is eliminated from the gastrointestinal tract. paregoric is a schedule lll narcotic. morphine can produce drug dependence and, therefore, has the potential for being abused. patients receiving therapeutic dosage regimens of 10 mg every 4 hours for 1 to 2 weeks have exhibited mild withdrawal symptoms. development of the dependent state is recognizable by an increased tolerance to the analgesic effect and the appearance of purposive phenomena (complaints, pleas, demands, or manipulative actions) shortly before the time of the next scheduled dose. a patient in withdrawal should be treated in a hospital environment. usually, it is necessary only to provide sup
United States -
English -
NLM (National Library of Medicine)
protriptyline hydrochloride tablet, film coated
hi-tech pharmacal co., inc. - protriptyline hydrochloride (unii: 44665v00o8) (protriptyline - unii:4ndu154t12) - protriptyline hydrochloride 5 mg - protriptyline hydrochloride tablets are indicated for the treatment of symptoms of mental depression in patients who are under close medical supervision. its activating properties make it particularly suitable for withdrawn and anergic patients. protriptyline hydrochloride tablets are contraindicated in patients who have shown prior hypersensitivity to it. it should not be given concomitantly with a monoamine oxidase inhibiting compound. hyperpyretic crises, severe convulsions, and deaths have occurred in patients receiving tricyclic antidepressant and monoamine oxidase inhibiting drugs simultaneously. when it is desired to substitute protriptyline for a monoamine oxidase inhibitor, a minimum of 14 days should be allowed to elapse after the latter is discontinued. protriptyline should then be initiated cautiously with gradual increase in dosage until optimum response is achieved. protriptyline is contraindicated in patients taking cisapride because of the possibility of adverse cardiac interactions includ
United States -
English -
NLM (National Library of Medicine)
lidocaine ointment
hi-tech pharmacal co., inc. - lidocaine (unii: 98pi200987) (lidocaine - unii:98pi200987) - lidocaine 5 g in 100 g - rx only lidocaine ointment 5% is indicated for production of anesthesia of accessible mucous membranes of the oropharynx. it is also useful as an anesthetic lubricant for intubation and for the temporary relief of pain associated with minor burns, including sunburn, abrasions of the skin, and insect bites. lidocaine is contraindicated in patients with a known history of hypersensitivity to local anesthetics of the amide type or to other components of lidocaine ointment 5%.
Australia -
English -
APVMA (Australian Pesticides and Veterinary Medicines Authority)
international biolux new technology trilux 33 hard antifouling for aluminium
akzo nobel pty limited - copper present as cuprous thiocyanate; zinc pyrithione - paint - copper present as cuprous thiocyanate cyanide active 125.0 g/l; zinc pyrithione mineral-zinc active 50.0 g/l - antifouling - boat - aluminium | aluminium boat - marine growth | barnacles | fresh-water fouling organisms | marine fouling organisms | mussels
