POLYMYXIN B- polymyxin b sulfate injection, powder, lyophilized, for solution Соединенные Штаты - английский - NLM (National Library of Medicine)

polymyxin b- polymyxin b sulfate injection, powder, lyophilized, for solution

fresenius kabi usa, llc - polymyxin b sulfate (unii: 19371312d4) (polymyxin b - unii:j2vz07j96k) - acute infections caused by susceptible strains of pseudomonas aeruginosa . polymyxin b sulfate is a drug of choice in the treatment of infections of the urinary tract, meninges, and blood-stream caused by susceptible strains of p. aeruginosa . it may also be used topically and subconjunctivally in the treatment of infections of the eye caused by susceptible strains of p. aeruginosa . it may be indicated in serious infections caused by susceptible strains of the following organisms, when less potentially toxic drugs are ineffective or contraindicated: h influenzae, specifically meningeal infections. escherichia coli, specifically urinary tract infections. aerobacter aerogenes, specifically bacteremia. klebsiella pneumoniae, specifically bacteremia. note: in meningeal infections, polymyxin b sulfate should be administered only by the intrathecal route. to reduce the development of drug-resistant bacteria and maintain the effectiveness of polymyxin b and other antibacterial drugs, polymyxin b should be used

POLYMYXIN B- polymyxin b sulfate injection, powder, lyophilized, for solution Соединенные Штаты - английский - NLM (National Library of Medicine)

polymyxin b- polymyxin b sulfate injection, powder, lyophilized, for solution

fresenius kabi usa, llc - polymyxin b sulfate (unii: 19371312d4) (polymyxin b - unii:j2vz07j96k) - acute infections caused by susceptible strains of pseudomonas aeruginosa . polymyxin b sulfate is a drug of choice in the treatment of infections of the urinary tract, meninges, and blood-stream caused by susceptible strains of p. aeruginosa . it may also be used topically and subconjunctivally in the treatment of infections of the eye caused by susceptible strains of p. aeruginosa . it may be indicated in serious infections caused by susceptible strains of the following organisms, when less potentially toxic drugs are ineffective or contraindicated: h influenzae, specifically meningeal infections. escherichia coli, specifically urinary tract infections. aerobacter aerogenes, specifically bacteremia. klebsiella pneumoniae, specifically bacteremia. note: in meningeal infections, polymyxin b sulfate should be administered only by the intrathecal route. to reduce the development of drug-resistant bacteria and maintain the effectiveness of polymyxin b and other antibacterial drugs, polymyxin b should be used

INDOMETHACIN injection, powder, lyophilized, for solution Соединенные Штаты - английский - NLM (National Library of Medicine)

indomethacin injection, powder, lyophilized, for solution

fresenius kabi usa, llc - indomethacin (unii: xxe1cet956) (indomethacin - unii:xxe1cet956) - indomethacin for injection is indicated to close a hemodynamically significant patent ductus arteriosus in premature infants weighing between 500 and 1,750 g when 48 hours usual medical management (e.g., fluid restriction, diuretics, digitalis, respiratory support, etc.) is ineffective. clear-cut clinical evidence of a hemodynamically significant patent ductus arteriosus should be present, such as respiratory distress, a continuous murmur, a hyperactive precordium, cardiomegaly, or pulmonary plethora on chest x-ray. indomethacin for injection is contraindicated in neonates: - with proven or suspected infection that is untreated - who are bleeding, especially those with active intracranial hemorrhage or gastrointestinal bleeding - with thrombocytopenia or coagulation defects - with or who are suspected of having necrotizing enterocolitis - with significant impairment of renal function - with congenital heart disease in whom patency of the ductus arteriosus is necessary for satisfactory pulmonary or systemic b

SODIUM CHLORIDE injection, solution, concentrate Соединенные Штаты - английский - NLM (National Library of Medicine)

sodium chloride injection, solution, concentrate

fresenius kabi usa, llc - sodium chloride (unii: 451w47iq8x) (sodium cation - unii:lyr4m0nh37, chloride ion - unii:q32zn48698) - 23.4% sodium chloride injection, usp is indicated for use as an electrolyte replenisher in parenteral fluid therapy. it serves as an additive for total parenteral nutrition (tpn) and as an additive for carbohydrate containing i.v. fluids. 23.4% sodium chloride injection, usp additive solution is contraindicated in patients with hypernatremia or fluid retention.

CARDIOPLEGIC SOLUTION- potassium chloride, sodium chloride, calcium chloride, and magnesium chloride injection, solution Соединенные Штаты - английский - NLM (National Library of Medicine)

cardioplegic solution- potassium chloride, sodium chloride, calcium chloride, and magnesium chloride injection, solution

fresenius kabi, usa, llc - potassium chloride (unii: 660yq98i10) (potassium cation - unii:295o53k152, chloride ion - unii:q32zn48698), sodium chloride (unii: 451w47iq8x) (sodium cation - unii:lyr4m0nh37, chloride ion - unii:q32zn48698), calcium chloride (unii: m4i0d6vv5m) (calcium cation - unii:2m83c4r6zb, chloride ion - unii:q32zn48698), magnesium chloride (unii: 02f3473h9o) (magnesium cation - unii:t6v3lhy838, chloride ion - unii:q32zn48698) - cardioplegic solution when suitably buffered in combination with ischemia and hypothermia is used to induce cardiac arrest during open heart surgery. cardioplegic solution must not be administered without the addition of 8.4% sodium bicarbonate injection, usp. not for intravenous injection. this solution is only for instillation into cardiac vasculature after buffering with sodium bicarbonate. flexible plastic container (free flex ® bag) do not remove solution container from its overwrap until immediately before use. the intact port cap provides visual tamper evidence. do not use if port cap is prematurely removed. maintain strict aseptic technique during handling. to open - always inspect the solution container before and after removal from the overwrap. - place the solution container on a clean, flat surface. remove the solution container from the overwrap. - check the solution container for leaks by squeezing firmly. if leaks are found, discard. to add 10 ml of 8.4% sodium bicarbonate injection, usp, and i

SODIUM ACETATE injection, solution, concentrate Соединенные Штаты - английский - NLM (National Library of Medicine)

sodium acetate injection, solution, concentrate

fresenius kabi usa, llc - sodium acetate (unii: 4550k0sc9b) (acetate ion - unii:569dqm74sc, sodium cation - unii:lyr4m0nh37) - sodium cation 328 mg in 100 ml - sodium acetate injection, usp (4 meq per ml) is indicated as a source of sodium for addition to large volume intravenous fluids to prevent or correct hyponatremia in patients with restricted or no oral intake. it is also useful as an additive for preparing specific intravenous fluid formulas when the needs of the patient cannot be met by standard electrolyte or nutrient solutions. sodium acetate injection, usp (4 meq per ml) is contraindicated in patients with hypernatremia or fluid retention.

SODIUM CHLORIDE- sodium chloride injection Соединенные Штаты - английский - NLM (National Library of Medicine)

sodium chloride- sodium chloride injection

fresenius kabi usa, llc - sodium chloride (unii: 451w47iq8x) (sodium cation - unii:lyr4m0nh37, chloride ion - unii:q32zn48698) - sodium chloride 9 mg in 1 ml - this parenteral preparation is indicated only for diluting or dissolving drugs for intravenous, intramuscular, or subcutaneous injection, according to instructions of the manufacturer of the drug to be administered.

SODIUM CHLORIDE injection, solution Соединенные Штаты - английский - NLM (National Library of Medicine)

sodium chloride injection, solution

fresenius kabi usa, llc - sodium chloride (unii: 451w47iq8x) (sodium cation - unii:lyr4m0nh37, chloride ion - unii:q32zn48698) - sodium chloride 9 mg in 1 ml - intravenous solutions containing sodium chloride are indicated for parenteral replenishment of fluid and sodium chloride as required by the clinical condition of the patient. none known. check flexible container solution composition, lot number, and expiry date. do not remove solution container from its overwrap until immediately before use. use sterile equipment and aseptic technique. to open - turn solution container over so that the text is face down. using the pre-cut corner tabs, peel open the overwrap and remove solution container. - check the solution container for leaks by squeezing firmly. if leaks are found, or if the seal is not intact, discard the solution. - do not use if the solution is cloudy or a precipitate is present. to add medication - identify white additive port with arrow pointing toward container. - immediately before injecting additives, break off white additive port cap with the arrow pointing toward container. - hold base of white additive port horizontally. - insert needle horizontally through the center of white additive port's septum and inject additives. - mix container contents thoroughly. preparation for administration - immediately before inserting the infusion set, break off blue infusion port cap with the arrow pointing away from container. - use a non-vented infusion set or close the air-inlet on a vented set. - close the roller clamp of the infusion set. - hold the base of blue infusion port. - insert spike through blue infusion port by rotating wrist slightly until the spike is inserted. note: see full directions accompanying administration set. warning: do not use flexible container in series connections.

HALOPERIDOL- haloperidol lactate injection, solution Соединенные Штаты - английский - NLM (National Library of Medicine)

haloperidol- haloperidol lactate injection, solution

fresenius kabi usa, llc - haloperidol lactate (unii: 6387s86pk3) (haloperidol - unii:j6292f8l3d) - haloperidol 5 mg in 1 ml - haloperidol injection is indicated for the treatment of patients with schizophrenia. haloperidol injection is contraindicated in patients with: - severe toxic central nervous system depression or comatose states from any cause. - hypersensitivity to this drug – hypersensitivity reactions have included anaphylactic reaction and angioedema (see warnings, hypersensitivity reactions and adverse reactions). - parkinson's disease (see warnings, neurological adverse reactions in patients with parkinson's disease or dementia with lewy bodies). - dementia with lewy bodies (see warnings, neurological adverse reactions in patients with parkinson's disease or dementia with lewy bodies).

ACYCLOVIR- acyclovir sodium injection, solution Соединенные Штаты - английский - NLM (National Library of Medicine)

acyclovir- acyclovir sodium injection, solution

fresenius kabi usa, llc - acyclovir sodium (unii: 927l42j563) (acyclovir - unii:x4hes1o11f) - acyclovir 50 mg in 1 ml - acyclovir sodium injection is indicated for the treatment of initial and recurrent mucosal and cutaneous herpes simplex (hsv-1 and hsv-2) in immunocompromised patients. acyclovir sodium injection is indicated for the treatment of severe initial clinical episodes of herpes genitalis in immuno-competent patients. acyclovir sodium injection is indicated for the treatment of herpes simplex encephalitis. acyclovir sodium injection is indicated for the treatment of neonates and infants with herpes simplex infections. acyclovir sodium injection is indicated for the treatment of varicella-zoster (shingles) infections in immunocompromised patients. acyclovir sodium injection is contraindicated for patients who develop hypersensitivity to acyclovir or valacyclovir.