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Searched for rapid. Results 201 to 210 of 541 total matches.

Gallium For Hypercalcemia of Malignancy

   
The Medical Letter on Drugs and Therapeutics • May 03, 1991  (Issue 843)
trials are available comparing gallium with plicamycin; plicamycin rapidly decreases serum calcium after ...
Gallium nitrate (Ganite - Fujisawa, USA), originally an anticancer drug, was recently marketed for treatment of cancer-associated hypercalcemia that has not responded to hydration. Other drugs used for treatment of hypercalcemia include furosemide (Lasix, and others), the bisphosphonate etidronate (Didronel IV), calcitonin (Calcimar), and plicamycin (Mithracin, formerly mithramycin) (RAB Schaiff et al, Clin Pharm, 8:108, 1989). Newer bisphosphonates are available in Europe.
Med Lett Drugs Ther. 1991 May 3;33(843):41-2 |  Show IntroductionHide Introduction

Fludarabine

   
The Medical Letter on Drugs and Therapeutics • Sep 20, 1991  (Issue 853)
— After intravenous infusion of fludarabine phosphate, the phosphate group is rapidly cleaved, leaving 2 ...
Fludarabine phosphate (Fludara - Berlex), an analog of vidarabine (Vira-A), was recently approved by the U.S. Food and Drug Administration for treatment of patients with refractory chronic lymphocytic leukemia (CLL). The drug has not yet been marketed but is still available, as it has been for two years, through the National Cancer Institute.
Med Lett Drugs Ther. 1991 Sep 20;33(853):89-90 |  Show IntroductionHide Introduction

Quinapril for Hypertension

   
The Medical Letter on Drugs and Therapeutics • Mar 20, 1992  (Issue 866)
— Quinapril is a pro-drug that is rapidly converted to its active form in the small intestine and the liver ...
Quinapril (Accupril - Parke-Davis), an angiotensin-converting enzyme (ACE) inhibitor, has been approved by the US Food and Drug Administration (FDA) for treatment of hypertension. ACE inhibitors are now widely used for this indication (Medical Letter, 33:33, 1991).
Med Lett Drugs Ther. 1992 Mar 20;34(866):27-8 |  Show IntroductionHide Introduction

Risperidone for Chronic Schizophrenia

   
The Medical Letter on Drugs and Therapeutics • Apr 15, 1994  (Issue 920)
to have a more rapid onset of action, producing clinical improvement after one week (RL Borison et al ...
Risperidone (Risperdal - Janssen), a benzisoxazole derivative, is now available in the USA for treatment of schizophrenia and other psychotic disorders.
Med Lett Drugs Ther. 1994 Apr 15;36(920):33-4 |  Show IntroductionHide Introduction

Aerosolized Deoxyribonuclease for Cystic Fibrosis

   
The Medical Letter on Drugs and Therapeutics • Apr 15, 1994  (Issue 920)
treatment stopped, pulmonary function tests and pulmonary symptoms rapidly returned to baseline. ADVERSE ...
Recombinant human deoxyribonuclease I (rhDNase; dornase alfa; Pulmozyme - Genentech), an enzyme that hydrolyzes extracellular DNA, is now available as a purified solution to decrease the viscosity of sputum in patients with cystic fibrosis. It requires a nebulizer to produce an aerosol mist for inhalation.
Med Lett Drugs Ther. 1994 Apr 15;36(920):34-5 |  Show IntroductionHide Introduction

Aprotinin To Decrease Bleeding in Cardiac Surgery

   
The Medical Letter on Drugs and Therapeutics • Jun 10, 1994  (Issue 924)
disappears rapidly from the circulation and is metabolized by lysosomal activity in the kidney ...
Aprotinin (Trasylol - Miles), an inhibitor of fibrinolysis first identified in 1930, was recently approved by the US Food and Drug Administration for intravenous use in high-risk coronary artery bypass graft (CABG) surgery to decrease bleeding and the need for transfusion. Inhibitors of fibrinolysis previously available in the USA include aminocaproic acid (Amicar, and others) and tranexamic acid (Cyklokapron - Medical Letter, 29:89, 1987).
Med Lett Drugs Ther. 1994 Jun 10;36(924):50-1 |  Show IntroductionHide Introduction

Yohimbine for Male Sexual Dysfunction

   
The Medical Letter on Drugs and Therapeutics • Dec 23, 1994  (Issue 938)
is not clear. Yohimbine is well absorbed from the gastrointestinal tract and disappears rapidly from the blood ...
Yohimbine hydrochloride, a presynaptic 2 -adrenergic receptor antagonist available by prescription in the USA (Yocon, Yohimex, and others), is advertised for treatment of impotence and has been used as an aphrodisiac. A pre-1938 drug, yohimbine has never been approved for marketing by the US Food and Drug Administration.
Med Lett Drugs Ther. 1994 Dec 23;36(938):115-6 |  Show IntroductionHide Introduction

Mycophenolate Mofetil - A New Immunosuppressant for Organ Transplantation

   
The Medical Letter on Drugs and Therapeutics • Sep 29, 1995  (Issue 958)
) and corticosteroids. MECHANISM OF ACTION — Mycophenolate mofetil is rapidly hydrolyzed in vivo to mycophenolic acid ...
Mycophenolate mofetil (CellCept - Roche) has been approved by the US Food and Drug Administration for oral use in preventing organ rejection in patients receiving allogeneic renal transplants. It is being promoted as an improvement over azathioprine (Imuran) for concurrent use with cyclosporine (Sandimmune; Neoral) and corticosteroids.
Med Lett Drugs Ther. 1995 Sep 29;37(958):84-6 |  Show IntroductionHide Introduction

Valacyclovir

   
The Medical Letter on Drugs and Therapeutics • Jan 05, 1996  (Issue 965)
; it has a bioavailability of 15% to 30%. Valacyclovir is more completely absorbed and is rapidly hydrolyzed to acyclovir ...
Valacyclovir (Valtrex - Glaxo Wellcome), an L- valyl ester of acyclovir (Zovirax), has been approved by the US Food and Drug Administration (FDA) for oral treatment of herpes zoster (shingles) in immunocompetent adults. Famciclovir (Famvir - Medical Letter, 36:97, 1994) is also available for this indication.
Med Lett Drugs Ther. 1996 Jan 5;38(965):3-4 |  Show IntroductionHide Introduction

New Uses of Thalidomide

   
The Medical Letter on Drugs and Therapeutics • Feb 16, 1996  (Issue 968)
in 10% to 50% of patients treated for lepromatous leprosy. Relief of symptoms and signs is rapid ...
Thalidomide is now available as an investigational drug in the USA. A synthetic derivative of glutamic acid, it was marketed in Europe in 1957 as a sedative but withdrawn four years later after being associated with severe human teratogenicity (PF DArcy and JP Griffin, Adverse Drug React Toxicol Rev, 13:65, 1994). The drug has since been found effective for several different indications.
Med Lett Drugs Ther. 1996 Feb 16;38(968):15-6 |  Show IntroductionHide Introduction