Results 281 to 290 of about 93,808 (329)
Some of the next articles are maybe not open access.

Gingival sequestration of nifedipine in nifedipine-induced gingival overgrowth

The Lancet, 1992
The mechanism of gingival overgrowth associated with long-term use of nifedipine and of other drugs that affect calcium homoeostasis, such as cyclosporin and phenytoin, is unknown. With an ultrasensitive assay, we measured the pharmacokinetics of nifedipine in plasma and gingival crevicular fluid (GCF) of nine patients receiving this drug for angina ...
Janice S. Ellis   +3 more
openaire   +3 more sources

Chitosan microspheres of nifedipine and nifedipine-cyclodextrin inclusion complexes

International Journal of Pharmaceutics, 1996
Chitosan microspheres of nifedipine and nifedipine cyclodextrin complexes were prepared by the glutaraldehyde cross-linking of chitosan. Microspheres having different degrees of swelling were made by varying the cross-linking density. Drug incorporation efficiencies exceeding 70 % could be achieved for this drug.
Ivan Jalšenjak   +3 more
openaire   +3 more sources

Pharmacokinetics of nifedipine.

International journal of clinical pharmacology research, 1985
The pharmacokinetics of a slow-release formulation of nifedipine were studied following oral administration of a single 20 mg tablet in nine young male volunteers. Blood samples were collected and nifedipine concentrations analysed by gas liquid chromatography.
PASANISI, FABRIZIO   +2 more
openaire   +2 more sources

Nifedipine in the treatment of hypertension

European Journal of Clinical Pharmacology, 1983
Nifedipine, a calcium antagonist with a predominant vasodilator action, was evaluated for the treatment of hypertension. A 20 mg-tablet, with a slower absorption and a more sustained blood-level than provided by the 10 mg-capsule was administered to 20 patients. The duration of the trial was 20 weeks.
S. Blake   +3 more
openaire   +3 more sources

Pharmacology of Nifedipine [PDF]

open access: possible, 1975
This paper is a brief synopsis of the main pharmacological properties of nifedipine in connection with a concept of its hemodynamic action.
openaire   +1 more source

Nifedipine in Antihypertensive Therapy

Archives of Internal Medicine, 1985
To the Editor. —We read with interest the article by Evans et al 1 in the May 1984Archives. Their results are similar to ours in demonstrating nifedipine efficacy as a substitute for hydralazine and captopril in combination antihypertensive therapy. 2 Recently, McAreavey et al 3 suggested hydralazine as the best third-line drug.
Ehud Grossman   +2 more
openaire   +3 more sources

Pharmacokinetics of nifedipine in Taiwanese

Biopharmaceutics & Drug Disposition, 2004
AbstractTo elucidate the pharmacokinetics of nifedipine in Taiwanese, a retrospective review of nifedipine bioequivalence studies completed in Taiwan in the past 5 years was conducted. A total of 198 healthy male volunteers were given a single dose of a 10 mg Adalat® capsule as a reference drug after overnight fasting.
Yow Shieng Uang   +3 more
openaire   +3 more sources

Nifedipine-Induced Hypokalemia

Drug Intelligence & Clinical Pharmacy, 1986
Nifedipine, a calcium-channel blocking agent, has been reported to cause many side effects, particularly in the cardiovascular system. A case of nifedipine-induced hypokalemia is presented, with a discussion on the presumable mechanism involved in this phenomenon.
Shoshana Armon, Moshe Tishler
openaire   +3 more sources

Nifedipine and Agranulocytosis

Annals of Internal Medicine, 1983
Excerpt To the editor: We write to report a case of agranulocytosis we believe was probably caused by nifedipine.
Richard H. Turner, Arnold J. Voth
openaire   +2 more sources

Nifedipine in Intestinal Colic

JAMA: The Journal of the American Medical Association, 1990
To the Editor.— Nifedipine, a calcium channel blocking agent, relaxes smooth muscle and has been widely used for the treatment of coronary insufficiency and hypertension. Used for its spasmolytic effect, nifedipine has been found to be effective in relieving acute and recurrent urinary colic. 1 It exhibits relaxant activity in the intestinal tract and
openaire   +3 more sources

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