KELAPRIL 20mg Nový Zéland - angličtina - Ministry for Primary Industries

kelapril 20mg

kela n.v. - benazepril hydrochloride - benazepril hydrochloride 100 g/kg - cardiovascular agent

SULFACETAMIDE SODIUM solution Spojené štáty - angličtina - NLM (National Library of Medicine)

sulfacetamide sodium solution

nucare pharmaceuticals,inc. - sulfacetamide sodium (unii: 4nrt660kjq) (sulfacetamide - unii:4965g3j0f5) - sulfacetamide sodium 100 mg in 1 ml - sulfacetamide sodium ophthalmic solution usp, 10% is indicated for the treatment of conjunctivitis and other superficial ocular infections due to susceptible microorganisms, and as an adjunctive in systemic sulfonamide therapy of trachoma: escherichia coli, staphylococcus aureus, streptococcus pneumoniae, streptococcus (viridans group), haemophilus influenzae, klebsiella species, and enterobacter species. topically applied sulfonamides do not provide adequate coverage against neisseria species, serratia marcescens and pseudomonas aeruginosa . a significant percentage of staphylococcal isolates are completely resistant to sulfa drugs. sulfacetamide sodium ophthalmic solution is contraindicated in individuals who have a hypersensitivity to sulfonamides or to any ingredient of the preparation.

SULFACETAMIDE SODIUM solution Spojené štáty - angličtina - NLM (National Library of Medicine)

sulfacetamide sodium solution

sandoz inc. - sulfacetamide sodium (unii: 4nrt660kjq) (sulfacetamide - unii:4965g3j0f5) - sulfacetamide sodium 100 mg in 1 ml - indications and usage: sulfacetamide sodium ophthalmic solution usp, 10% is indicated for the treatment of conjunctivitis and other superficial ocular infections due to susceptible microorganisms, and as an adjunctive in systemic sulfonamide therapy of trachoma: escherichia coli, staphylococcus aureus, streptococcus pneumoniae, streptococcus (viridans group), haemophilus influenzae, klebsiella species, and enterobacter species. topically applied sulfonamides do not provide adequate coverage against neisseria species, serratia marcescens and pseudomonas aeruginosa . a significant percentage of staphylococcal isolates are completely resistant to sulfa drugs. contraindications: sulfacetamide sodium ophthalmic solution is contraindicated in individuals who have a hypersensitivity to sulfonamides or to any ingredient of the preparation.

CARISOPRODOL- carisoprodol tablet Spojené štáty - angličtina - NLM (National Library of Medicine)

carisoprodol- carisoprodol tablet

west-ward pharmaceutical corp - carisoprodol (unii: 21925k482h) (carisoprodol - unii:21925k482h) - carisoprodol 350 mg - carisoprodol tablets are indicated for the relief of discomfort associated with acute, painful musculoskeletal conditions in adults. carisoprodol tablets should only be used for short periods (up to two or three weeks) because adequate evidence of effectiveness for more prolonged use has not been established and because acute, painful musculoskeletal conditions are generally of short duration [see dosage and administration (2) ]. carisoprodol tablets are contraindicated in patients with a history of acute intermittent porphyria or a hypersensitivity reactions to a carbamate such as meprobamate there are no data on the use of carisoprodol tablets during human pregnancy. animal studies indicate that carisoprodol crosses the placenta and results in adverse effects on fetal growth and postnatal survival. the primary metabolite of carisoprodol, meprobamate, is an approved anxiolytic. retrospective, post-marketing studies do not show a consistent association between maternal use of meprobamate and an increase

SULFACETAMIDE SODIUM solution Spojené štáty - angličtina - NLM (National Library of Medicine)

sulfacetamide sodium solution

h.j. harkins company, inc. - sulfacetamide sodium (unii: 4nrt660kjq) (sulfacetamide - unii:4965g3j0f5) - sulfacetamide sodium 100 mg in 1 ml - sulfacetamide sodium ophthalmic solution usp, 10% is indicated for the treatment of conjunctivitis and other superficial ocular infections due to susceptible microorganisms, and as an adjunctive in systemic sulfonamide therapy of trachoma: escherichia coli, staphylococcus aureus, streptococcus pneumoniae, streptococcus (viridans group), haemophilus influenzae, klebsiella species, and enterobacter species. topically applied sulfonamides do not provide adequate coverage against neisseria species, serratia marcescens and pseudomonas aeruginosa . a significant percentage of staphylococcal isolates are completely resistant to sulfa drugs. sulfacetamide sodium ophthalmic solution is contraindicated in individuals who have a hypersensitivity to sulfonamides or to any ingredient of the preparation.

BISMUTH SUBSALICYLATE MAXIMUM STRENGTH STOMACH RELIEF- bismuth subsalicylate liquid Spojené štáty - angličtina - NLM (National Library of Medicine)

bismuth subsalicylate maximum strength stomach relief- bismuth subsalicylate liquid

aurohealth llc - bismuth subsalicylate (unii: 62tey51rr1) (salicylic acid - unii:o414pz4lpz, bismuth cation - unii:zs9cd1i8ye) - bismuth subsalicylate 1050 mg in 30 ml - upset stomach reliever and antidiarrheal relieves - travelers’ diarrhea - diarrhea - upset stomach due to overindulgence in food and drink, including: heartburn indigestion nausea gas belching fullness - heartburn - indigestion - nausea - gas - belching - fullness - an ulcer - a bleeding problem - bloody or black stool - fever - mucus in the stool - anticoagulation (thinning the blood) - diabetes - gout - arthritis when using this product a temporary, but harmless, darkening of the stool and/or tongue may occur - symptoms get worse - ringing in the ears or loss of hearing occurs - diarrhea lasts more than 2 days if pregnant or breast feeding, ask a health professional before use.

STOMACH RELIEF MAXIMUM STRENGTH- bismuth subsalicylate liquid Spojené štáty - angličtina - NLM (National Library of Medicine)

stomach relief maximum strength- bismuth subsalicylate liquid

cvs pharmacy, inc. - bismuth subsalicylate (unii: 62tey51rr1) (salicylic acid - unii:o414pz4lpz, bismuth cation - unii:zs9cd1i8ye) - bismuth subsalicylate 1050 mg in 30 ml - upset stomach reliever and antidiarrheal relieves - travelers’ diarrhea - diarrhea - upset stomach due to overindulgence in food and drink, including: heartburn indigestion nausea gas belching fullness - heartburn - indigestion - nausea - gas - belching - fullness - an ulcer - a bleeding problem - bloody or black stool - fever - mucus in the stool - anticoagulation (thinning the blood) - diabetes - gout - arthritis when using this product a temporary, but harmless, darkening of the stool and/or tongue may occur - symptoms get worse - ringing in the ears or loss of hearing occurs - diarrhea lasts more than 2 days if pregnant or breast feeding, ask a health professional before use.

STRATUSCARE ANTACID AND ANTIGAS REGULAR STRENGTH dimethicone aluminum hydroxide magnesium suspension Spojené štáty - angličtina - NLM (National Library of Medicine)

stratuscare antacid and antigas regular strength dimethicone aluminum hydroxide magnesium suspension

stratus pharmaceuticals - dimethicone (unii: 92ru3n3y1o) (dimethicone - unii:92ru3n3y1o) - dimethicone 20 mg in 5 ml

STRATUSCARE ANTACID AND ANTIGAS dimethicone aluminum hydroxide magnesium suspension Spojené štáty - angličtina - NLM (National Library of Medicine)

stratuscare antacid and antigas dimethicone aluminum hydroxide magnesium suspension

stratus pharamceuticals - dimethicone (unii: 92ru3n3y1o) (dimethicone - unii:92ru3n3y1o) - dimethicone 40 mg in 5 ml

STRATUSCARE ANTACID AND ANTIGAS aluminum hydroxide magnesium simethicone suspension Spojené štáty - angličtina - NLM (National Library of Medicine)

stratuscare antacid and antigas aluminum hydroxide magnesium simethicone suspension

stratus pharamceuticals - dimethicone (unii: 92ru3n3y1o) (dimethicone - unii:92ru3n3y1o) - dimethicone 20 mg in 5 ml