bextra- valdecoxib tablet, film coated
g.d. searle llc - valdecoxib (unii: 2919279q3w) (valdecoxib - unii:2919279q3w) - tablet, film coated - 10 mg - bextra tablets are indicated: - for relief of the signs and symptoms of osteoarthritis and adult rheumatoid arthritis. - for the treatment of primary dysmenorrhea. bextra should not be given to patients who have demonstrated allergic-type reactions to sulfonamides. bextra tablets are contraindicated in patients with known hypersensitivity to valdecoxib. bextra should not be given to patients who have experienced asthma, urticaria, or allergic-type reactions after taking aspirin or nsaids. severe, rarely fatal, anaphylactic-like reactions to nsaids are possible in such patients (see warnings — anaphylactoid reactions, and precautions — preexisting asthma). bextra is contraindicated for the treatment of post-operative pain immediately following coronary artery bypass graft (cabg) surgery and should not be used in this setting. (see clinical studies — safety studies).
bextra
pfizer new zealand limited - valdecoxib 20mg; ; - film coated tablet - 20 mg - active: valdecoxib 20mg excipient: croscarmellose sodium lactose monohydrate magnesium stearate microcrystalline cellulose opadry white purified water starch
bextra 20mg tablets
pfizer ltd - valdecoxib - oral tablet - 20mg
dynastat
pfizer new zealand limited - parecoxib sodium 21.18mg equivalent to 20 mg parecoxib; - powder for injection - 20 mg - active: parecoxib sodium 21.18mg equivalent to 20 mg parecoxib excipient: dibasic sodium phosphate heptahydrate nitrogen phosphoric acid sodium hydroxide hydrochloric acid nitrogen sodium chloride sodium hydroxide water for injection - for a single peri-operative dose for the management of post-operative pain.
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bextra film coated tablet 20 mg
yousif mahmood hussain pharmacy - valdecoxib - film coated tablet - 20