LITHIUM CARBONATE ER- lithium carbonate tablet মার্কিন যুক্তরাষ্ট্র - ইংরেজি - NLM (National Library of Medicine)

lithium carbonate er- lithium carbonate tablet

glenmark pharmaceuticals inc., usa - lithium carbonate (unii: 2bmd2gna4v) (lithium cation - unii:8h8z5uer66) - lithium carbonate 450 mg - lithium carbonate extended-release tablets are indicated in the treatment of manic episodes of manic-depressive illness. maintenance therapy prevents or diminishes the intensity of subsequent episodes in those manic-depressive patients with a history of mania. typical symptoms of mania include pressure of speech, motor hyperactivity, reduced need for sleep, flight of ideas, grandiosity, elation, poor judgment, aggressiveness and possibly hostility. when given to a patient experiencing a manic episode, lithium carbonate extended-release tablets may produce a normalization of symptomatology within 1 to 3 weeks.

LITHIUM CARBONATE tablet, extended release মার্কিন যুক্তরাষ্ট্র - ইংরেজি - NLM (National Library of Medicine)

lithium carbonate tablet, extended release

mylan pharmaceuticals inc. - lithium carbonate (unii: 2bmd2gna4v) (lithium cation - unii:8h8z5uer66) - lithium carbonate 450 mg - lithium carbonate extended-release tablets are indicated in the treatment of manic episodes of manic-depressive illness. maintenance therapy prevents or diminishes the intensity of subsequent episodes in those manic-depressive patients with a history of mania. typical symptoms of mania include pressure of speech, motor hyperactivity, reduced need for sleep, flight of ideas, grandiosity, elation, poor judgment, aggressiveness and possibly hostility. when given to a patient experiencing a manic episode, lithium carbonate extended-release tablets may produce a normalization of symptomatology within 1 to 3 weeks.

LITHIUM CARBONATE tablet, extended release মার্কিন যুক্তরাষ্ট্র - ইংরেজি - NLM (National Library of Medicine)

lithium carbonate tablet, extended release

mylan institutional inc. - lithium carbonate (unii: 2bmd2gna4v) (lithium cation - unii:8h8z5uer66) - lithium carbonate 450 mg - lithium carbonate extended-release tablets are indicated in the treatment of manic episodes of manic-depressive illness. maintenance therapy prevents or diminishes the intensity of subsequent episodes in those manic-depressive patients with a history of mania. typical symptoms of mania include pressure of speech, motor hyperactivity, reduced need for sleep, flight of ideas, grandiosity, elation, poor judgment, aggressiveness and possibly hostility. when given to a patient experiencing a manic episode, lithium carbonate extended-release tablets may produce a normalization of symptomatology within 1 to 3 weeks.

SEVELAMER CARBONATE tablet, film coated
SEVELAMER CARBONATE powder, for suspension মার্কিন যুক্তরাষ্ট্র - ইংরেজি - NLM (National Library of Medicine)

sevelamer carbonate tablet, film coated sevelamer carbonate powder, for suspension

winthrop u.s, a business of sanofi-aventis u.s. llc - sevelamer carbonate (unii: 9ycx42i8iu) (sevelamer - unii:941n5duu5c) - sevelamer carbonate 800 mg - sevelamer carbonate is indicated for the control of serum phosphorus in adults and children 6 years of age and older with chronic kidney disease (ckd) on dialysis. sevelamer carbonate is contraindicated in patients with bowel obstruction. sevelamer carbonate is contraindicated in patients with known hypersensitivity to sevelamer carbonate, sevelamer hydrochloride, or to any of the excipients. risk summary sevelamer carbonate is not absorbed systemically following oral administration and maternal use is not expected to result in fetal exposure to the drug. clinical considerations sevelamer carbonate may decrease serum levels of fat-soluble vitamins and folic acid in pregnant women [see clinical pharmacology (12.2)] . consider supplementation. data animal data in pregnant rats given dietary doses of 0.5, 1.5, or 4.5 g/kg/day of sevelamer hydrochloride during organogenesis, reduced or irregular ossification of fetal bones, probably due to a reduced absorption of fat-soluble vitamin d, occurred in mid and high-dose groups (human equivalent doses approximately equal to 3–4 times the maximum clinical trial dose of 13 g). in pregnant rabbits given oral doses of 100, 500, or 1000 mg/kg/day of sevelamer hydrochloride by gavage during organogenesis, an increase of early resorptions occurred in the high-dose group (human equivalent dose twice the maximum clinical trial dose). risk summary sevelamer carbonate is not absorbed systemically by the mother following oral administration, and breastfeeding is not expected to result in exposure of the child to sevelamer carbonate. clinical considerations sevelamer carbonate may decrease serum levels of fat-soluble vitamins and folic acid in pregnant women [see clinical pharmacology (12.2)] . consider supplementation. the safety and efficacy of sevelamer carbonate in lowering serum phosphorus levels was studied in patients 6 years of age and older with ckd. in this study, sevelamer carbonate was apparently less effective in children with a low baseline serum phosphorus, which described children <13 years of age and children not on dialysis. given its mechanism of action, sevelamer carbonate is expected to be effective in lowering serum phosphorus levels in pediatric patients with ckd. most adverse events that were reported as related, or possibly related, to sevelamer carbonate were gastrointestinal in nature. no new risks or safety signals were identified with the use of sevelamer carbonate in the trial. sevelamer carbonate has not been studied in pediatric patients below 6 years of age. clinical studies of sevelamer carbonate did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. other reported clinical experience has not identified differences in responses between the elderly and younger patients. in general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range.

LITHIUM CARBONATE tablet, extended release মার্কিন যুক্তরাষ্ট্র - ইংরেজি - NLM (National Library of Medicine)

lithium carbonate tablet, extended release

american health packaging - lithium carbonate (unii: 2bmd2gna4v) (lithium cation - unii:8h8z5uer66) - lithium carbonate 450 mg - lithium carbonate extended-release tablets are indicated in the treatment of manic episodes of manic-depressive illness. maintenance therapy prevents or diminishes the intensity of subsequent episodes in those manic-depressive patients with a history of mania. typical symptoms of mania include pressure of speech, motor hyperactivity, reduced need for sleep, flight of ideas, grandiosity, elation, poor judgment, aggressiveness and possibly hostility. when given to a patient experiencing a manic episode, lithium carbonate extended-release tablets may produce a normalization of symptomatology within 1 to 3 weeks.

Gaviscon Liquid Sachets Oral Suspension Sodium alginate 500mg, Sodium bicarbonate 267mg, Calcium carbonate 160mg আয়ার্লণ্ড - ইংরেজি - HPRA (Health Products Regulatory Authority)

gaviscon liquid sachets oral suspension sodium alginate 500mg, sodium bicarbonate 267mg, calcium carbonate 160mg

reckitt benckiser ireland ltd - sodium alginate; sodium bicarbonate; calcium carbonate - oral suspension in sachet - 500 mg+267 mg+160 milligram(s) - other drugs for peptic ulcer and gastro-oesophageal reflux disease (gord); alginic acid

Acidex Oral Suspension, Sodium Alginate 500mg, Sodium Bicarbonate 267mg, Calcium Carbonate 160mg/10ml আয়ার্লণ্ড - ইংরেজি - HPRA (Health Products Regulatory Authority)

acidex oral suspension, sodium alginate 500mg, sodium bicarbonate 267mg, calcium carbonate 160mg/10ml

pinewood laboratories ltd - sodium alginate; sodium bicarbonate; calcium carbonate - oral suspension - 500mg+267mg+160 milligram/ 10 millilitre - salt solutions; sodium bicarbonate

Gaviscon Advance Peppermint Oral Suspension Sachets   Sodium Alginate 500mg, Potassium hydrogen carbonate 100 mg Oral suspension. আয়ার্লণ্ড - ইংরেজি - HPRA (Health Products Regulatory Authority)

gaviscon advance peppermint oral suspension sachets sodium alginate 500mg, potassium hydrogen carbonate 100 mg oral suspension.

reckitt benckiser ireland ltd - sodium alginate; potassium hydrogen carbonate - oral suspension - 1000/200 milligram(s) - other drugs for peptic ulcer and gastro-oesophageal reflux disease (gord); alginic acid

Gaviscon Advance Peppermint Oral Suspension Sodium alginate 500 mg, Potassium hydrogen carbonate 100 mg. আয়ার্লণ্ড - ইংরেজি - HPRA (Health Products Regulatory Authority)

gaviscon advance peppermint oral suspension sodium alginate 500 mg, potassium hydrogen carbonate 100 mg.

reckitt benckiser ireland ltd - sodium alginate; potassium hydrogen carbonate - oral suspension - 1000/200 milligram(s) - other drugs for peptic ulcer and gastro-oesophageal reflux disease (gord); alginic acid