Search Results for "Drug Interactions"
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Searched for Drug Interactions. Results 1051 to 1060 of 1090 total matches.

Safety of Terfenadine and Astemizole

   
The Medical Letter on Drugs and Therapeutics • Feb 07, 1992  (Issue 863)
Nizoral ketoconazole with terfenadine Interactions drug ...
Terfenadine (Seldane - Marion Merrell Dow) and astemizole (Hismanal - Janssen) are nonsedating antihistamines widely used to treat symptoms of allergic rhinitis (Medical Letter, 27:65, 1985; 31:43, 1989). Both are available without a prescription in Canada, and the US Food and Drug Administration is apparently considering terfenadine for over-the-counter availability in the USA.
Med Lett Drugs Ther. 1992 Feb 7;34(863):9-10 | Show Introduction Hide Introduction

Prevention of Pneumocystis Carinii Pneumonia

   
The Medical Letter on Drugs and Therapeutics • Oct 07, 1988  (Issue 776)
The Medical Letter  On Drugs and Therapeutics www.medletter.com Published by The Medical ...
Pneumocystis carinii pneumonia (PCP) is a common cause of death in patients with acquired immune deficiency syndrome (AIDS). PCP is the first serious opportunistic infection in more than 60% of patients with AIDS, and about 80% of AIDS patients develop PCP at least once (AE Glatt et al, N Engl J Med, 318:1439, June 2, 1988). Many studies using drugs to prevent PCP in patients with AIDS have recently been reported.
Med Lett Drugs Ther. 1988 Oct 7;30(776):94-5 | Show Introduction Hide Introduction

Tislelizumab (Tevimbra) for Esophageal Cancer (online only)

   
The Medical Letter on Drugs and Therapeutics • May 13, 2024  (Issue 1702)
for second-line treatment. All of these drugs can cause significant toxicity.1,2 CLINICAL STUDIES ― FDA ...
The FDA has approved tislelizumab (Tevimbra – BeiGene), a programmed death receptor-1 (PD-1) blocking antibody, for treatment of unresectable or metastatic esophageal squamous cell cancer in adults who received prior systemic chemotherapy that did not include a programmed death ligand-1 (PD-L1) inhibitor.
Med Lett Drugs Ther. 2024 May 13;66(1702):e85-6   doi:10.58347/tml.2024.1702h | Show Introduction Hide Introduction

Two New Amphetamines for ADHD

   
The Medical Letter on Drugs and Therapeutics • Jun 20, 2016  (Issue 1497)
The Medical Letter® on Drugs and Therapeutics Volume 58 (Issue 1497) June 20, 2016 Take CME ...
Two new extended-release amphetamine products have been approved by the FDA for once-daily treatment of attention-deficit/hyperactivity disorder (ADHD) in patients ≥6 years old: Adzenys XR-ODT (Neos Therapeutics), an orally distintegrating tablet, and Dyanavel XR (Tris Pharma), an oral suspension.
Med Lett Drugs Ther. 2016 Jun 20;58(1497):80-1 | Show Introduction Hide Introduction

Intravenous Ciprofloxacin

   
The Medical Letter on Drugs and Therapeutics • Aug 09, 1991  (Issue 850)
cyclosporine Fortaz Imipenem-cilastatin sodium Interactions drug with ciprofloxacin intravenous ...
Ciprofloxacin, previously available orally (Cipro - Medical Letter, 30:11, 1988) and for ophthalmic use (Ciloxan - Medical Letter, 33:52, May 31, 1991), is now the first fluoroquinolone antibiotic to become available in the USA in an intravenous (IV) formulation. Cipro I.V. (Miles) is being promoted as an alternative to third-generation cephalosporins, aminoglycosides, and other drugs used for treatment of serious infections.
Med Lett Drugs Ther. 1991 Aug 9;33(850):75-6 | Show Introduction Hide Introduction

Cefditoren (Spectracef) - A New Oral Cephalosporin

   
The Medical Letter on Drugs and Therapeutics • Jan 21, 2002  (Issue 1122)
The Medical Letter  On Drugs and Therapeutics www.medletter.com Published by The Medical ...
Cefditoren pivoxil (Spectracef — TAP), a new oral third-generation cephalosporin, has been approved by the FDA for treatment of acute exacerbations of chronic bronchitis, pharyngitis, tonsillitis and uncomplicated skin and soft tissue infections in adults and children 12 or more years old. The drug has been used in Japan for 7 years.
Med Lett Drugs Ther. 2002 Jan 21;44(1122):5-6 | Show Introduction Hide Introduction

Fluoxetine For Depression

   
The Medical Letter on Drugs and Therapeutics • Apr 22, 1988  (Issue 764)
The Medical Letter  On Drugs and Therapeutics www.medletter.com Published by The Medical ...
Fluoxetine (Prozac - Dista), a phenylpropylamide, is the first serotonin-reuptake blocker introduced in the USA for treatment of . It is being promoted as causing fewer adverse effects than other antidepressants. Claims of greater safety and patient tolerability have often been made for new non-tricyclic antidepressants in recent years, but unpredicted adverse effects have emerged with widespread use, including priapism with trazodone (Desyrel - Medical Letter, 26:35, 1984) and fatal hemolytic anemia with nomifensine (Merital - Medical Letter, 27:73, 1985).
Med Lett Drugs Ther. 1988 Apr 22;30(764):45-7 | Show Introduction Hide Introduction

Granisetron to Prevent Vomiting After Cancer Chemotherapy

   
The Medical Letter on Drugs and Therapeutics • Jul 08, 1994  (Issue 926)
affect the clearance of granisetron, but clinically relevant interactions with other drugs ...
Granisetron, a serotonin (5-HT) antagonist similar to ondansetron, was recently approved by the US Food and Drug Administration for prevention of nausea and vomiting due to cancer chemotherapy. Although available in an oral formulation in other countries, granisetron is available here only for intravenous (IV) use.
Med Lett Drugs Ther. 1994 Jul 8;36(926):61-2 | Show Introduction Hide Introduction

Altuviiio – A Longer-Acting Factor VIII Product for Hemophilia A

   
The Medical Letter on Drugs and Therapeutics • May 01, 2023  (Issue 1675)
replacement therapy. FACTOR VIII PRODUCTS ― The interaction between factor VIII and VWF imposes a ceiling ...
The FDA has approved Altuviiio (Sanofi), a von Willebrand Factor (VWF)-independent, recombinant factor VIII concentrate, for routine prophylaxis, on-demand treatment to control bleeding episodes, and perioperative management of bleeding in children and adults with hemophilia A. The manufacturer claims that Altuviiio, which was previously called efanesoctocog alfa, delivers normal to near-normal factor VIII levels for most of the week with once-weekly intravenous dosing.
Med Lett Drugs Ther. 2023 May 1;65(1675):67-8   doi:10.58347/tml.2023.1675b | Show Introduction Hide Introduction

Toripalimab (Loqtorzi) for Nasopharyngeal Carcinoma (online only)

   
The Medical Letter on Drugs and Therapeutics • Jan 22, 2024  (Issue 1694)
receptors, blocking its interaction with PD-L1 and PD-L2 and restoring T cell antitumor immune responses ...
Toripalimab-tpzi (Loqtorzi – Coherus Biosciences), a programmed death receptor-1 (PD-1)-blocking antibody, has been approved by the FDA for use in combination with cisplatin and gemcitabine for first-line treatment of recurrent locally advanced or metastatic nasopharyngeal carcinoma and for use as monotherapy for treatment of recurrent unresectable or metastatic nasopharyngeal carcinoma in adults with disease progression on or after platinum-based chemotherapy. It is the first immune checkpoint inhibitor to be approved in the US for treatment of nasopharyngeal carcinoma.
Med Lett Drugs Ther. 2024 Jan 22;66(1694):e16-7   doi:10.58347/tml.2024.1694e | Show Introduction Hide Introduction