intron a kit
merck canada inc - interferon alfa-2b; water - kit - 18miu; 1ml - interferon alfa-2b 18miu; water 1ml - interferons
intron a liquid
merck canada inc - interferon alfa-2b - liquid - 15000000unit - interferon alfa-2b 15000000unit - interferons
intron a liquid
merck canada inc - interferon alfa-2b - liquid - 25000000unit - interferon alfa-2b 25000000unit - interferons
intron a liquid
merck canada inc - interferon alfa-2b - liquid - 50000000unit - interferon alfa-2b 50000000unit - interferons
dalfampridine tablet, film coated, extended release
actavis pharma, inc. - dalfampridine (unii: bh3b64okl9) (dalfampridine - unii:bh3b64okl9) - dalfampridine extended-release tablets are indicated as a treatment to improve walking in adult patients with multiple sclerosis (ms). this was demonstrated by an increase in walking speed [see clinical studies (14)]. the use of dalfampridine is contraindicated in the following conditions: - history of seizure [see warnings and precautions (5.1)] - moderate or severe renal impairment (crcl ≤50 ml/min) [see warnings and precautions (5.2)] - history of hypersensitivity to dalfampridine or 4-aminopyridine; reactions have included anaphylaxis [see warnings and precautions (5.4)] risk summary there are no adequate data on the developmental risk associated with use of dalfampridine in pregnant women. administration of dalfampridine to animals during pregnancy and lactation resulted in decreased offspring viability and growth at clinically relevant doses [see data] . in the u.s. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2 to 4% an
roferon-a solution 3 million i.u./ml
hoffmann-la roche limited - interferon alpha-2a - solution - 3m - interferon alpha-2a 3m - antineoplastic agents
roferon-a soln-liq im sc 9million i.u./ml solution
hoffmann-la roche limited - interferon alpha-2a - solution - 9m - interferon alpha-2a 9m - antineoplastic agents
roferon-a solution 18 million i.u./3ml
hoffmann-la roche limited - interferon alpha-2a - solution - 18m - interferon alpha-2a 18m - antineoplastic agents
dalfampridine tablet, film coated, extended release
ascend laboratories, llc - dalfampridine (unii: bh3b64okl9) (dalfampridine - unii:bh3b64okl9) - dalfampridine extended-release tablets are indicated as a treatment to improve walking in adult patients with multiple sclerosis (ms). this was demonstrated by an increase in walking speed [see clinical studies (14)]. the use of dalfampridine extended-release tablets are contraindicated in the following conditions: - history of seizure [see warnings and precautions (5.1)] - moderate or severe renal impairment (crcl≤50 ml/min) [see warnings and precautions (5.2)] - history of hypersensitivity to dalfampridine extended-release tablets or 4-aminopyridine; reactions have included anaphylaxis [see warnings and precautions (5.4)] risk summary there are no adequate data on the developmental risk associated with use of dalfampridine extended-release tablets in pregnant women. administration of dalfampridine to animals during pregnancy and lactation resulted in decreased offspring viability and growth at clinically relevant doses [see data]. in the u.s. general population, the estimated background risk of major bi
dalfampridine tablet, film coated, extended release
bryant ranch prepack - dalfampridine (unii: bh3b64okl9) (dalfampridine - unii:bh3b64okl9) - dalfampridine extended-release tablets are indicated as a treatment to improve walking in adult patients with multiple sclerosis (ms). this was demonstrated by an increase in walking speed [see clinical studies (14)]. the use of dalfampridine extended-release tablets are contraindicated in the following conditions: - history of seizure [see warnings and precautions (5.1)] - moderate or severe renal impairment (crcl≤50 ml/min) [see warnings and precautions (5.2)] - history of hypersensitivity to dalfampridine extended-release tablets or 4-aminopyridine; reactions have included anaphylaxis [see warnings and precautions (5.4)] risk summary there are no adequate data on the developmental risk associated with use of dalfampridine extended-release tablets in pregnant women. administration of dalfampridine to animals during pregnancy and lactation resulted in decreased offspring viability and growth at clinically relevant doses [see data]. in the u.s. general population, the estimated background risk of major birt