Search Results for "A-200"
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Searched for A-200. Results 261 to 270 of 665 total matches.

Penpulimab (Anniko) for Nasopharyngeal Carcinoma (online only)

   
The Medical Letter on Drugs and Therapeutics • Jul 21, 2025  (Issue 1733)
or metastatic nonkeratinizing nasopharyngeal carcinoma is 200 mg administered IV once every 3 weeks until ...
Penpulimab-kcqx (Anniko – Akeso Biopharma), a programmed death receptor-1 (PD-1)-blocking antibody, has been approved by the FDA for use in combination with cisplatin or carboplatin plus gemcitabine for first-line treatment of recurrent or metastatic nonkeratinizing nasopharyngeal carcinoma and for use as monotherapy for metastatic disease in adults with disease progression on or after platinum-based chemotherapy and at least one other prior line of therapy. Penpulimab is the second immune checkpoint inhibitor to be approved in the US for treatment of nasopharyngeal carcinoma;...
Med Lett Drugs Ther. 2025 Jul 21;67(1733):e122-3   doi:10.58347/tml.2025.1733k |  Show IntroductionHide Introduction

COVID-19 Update: Remdesivir (Veklury) FDA-Approved for Children <12 Years Old (online only)

   
The Medical Letter on Drugs and Therapeutics • Jun 13, 2022  (Issue 1652)
is 5 mg/kg (max 200 mg) on day 1 and 2.5 mg/kg (max 100 mg) on subsequent days. Treatment should ...
IV antiviral drug remdesivir (Veklury) has now been FDA-approved for treatment of COVID-19 in patients ≥28 days old who weigh ≥3 kg and are either hospitalized or at high risk for progression to severe disease. Remdesivir was already FDA-approved for these indications in patients ≥12 years old who weigh ≥40 kg; it was available under an Emergency Use Authorization (EUA) for younger or lighter patients. Remdesivir is the first drug to be FDA-approved for treatment of COVID-19 in children <12 years old.
Med Lett Drugs Ther. 2022 Jun 13;64(1652):e1 |  Show IntroductionHide Introduction

Paliperidone (Invega) for Schizophrenia

   
The Medical Letter on Drugs and Therapeutics • Mar 12, 2007  (Issue 1256)
Discmelt 2 455.70 Clozapine – generic 100-200 mg 243.00 Clozaril (Novartis) tid 474.30 Fazaclo 2 ...
Paliperidone (Invega - Janssen) has been approved by the FDA in an extended-release formulation for treatment of schizophrenia. It is the primary active metabolite of the second-generation antipsychotic risperidone (Risperdal - Janssen), which is scheduled to lose its patent exclusivity in December 2007.
Med Lett Drugs Ther. 2007 Mar 12;49(1256):21-3 |  Show IntroductionHide Introduction

Golimumab (Simponi) for Inflammatory Arthritis

   
The Medical Letter on Drugs and Therapeutics • Jul 13, 2009  (Issue 1316)
q2wks $1620.00 Certolizumab – Cimzia (UCB) Humanized 200 mg vial; 200 mg/mL 400 mg SC at 0, 2 and 4 wks ...
Golimumab (Simponi - Centocor), a fully humanized anti-tumor necrosis factor (TNF)-a antibody, has been approved by the FDA for the treatment of: (1) moderate to severe active rheumatoid arthritis (RA) in combination with methotrexate; (2) active psoriatic arthritis (PsA) alone or in combination with methotrexate; and (3) active ankylosing spondylitis (AS).
Med Lett Drugs Ther. 2009 Jul 13;51(1316):55-6 |  Show IntroductionHide Introduction

Iloperidone (Fanapt) - Another Second-Generation Antipsychotic

   
The Medical Letter on Drugs and Therapeutics • Feb 22, 2010  (Issue 1332)
First Generation Chlorpromazine – generic 200 mg bid $ 56.40 Fluphenazine – generic 10 mg 1x/d 4.00 2 ...
The FDA has approved the marketing of iloperidone (Fanapt – Vanda), a second-generation antipsychotic, for treatment of schizophrenia. Iloperidone is chemically related to risperidone (Risperdal, and others).
Med Lett Drugs Ther. 2010 Feb 22;52(1332):13-4 |  Show IntroductionHide Introduction

Odefsey - Another NNRTI Combination for HIV

   
The Medical Letter on Drugs and Therapeutics • May 09, 2016  (Issue 1494)
Dosage Cost1 Efavirenz/emtricitabine/TDF – Atripla 600/200/300 mg 1 tab once/d2,3 $2391.60 (Gilead/BMS ...
The FDA has approved Odefsey (Gilead), a once-daily, fixed-dose combination of the non-nucleoside reverse transcriptase inhibitor (NNRTI) rilpivirine and the nucleoside/nucleotide reverse transcriptase inhibitors (NRTIs) emtricitabine and tenofovir alafenamide, for initial treatment of HIV-1 infection in patients with HIV-1 RNA (viral load) ≤100,000 copies/mL or to replace a stable antiretroviral regimen in patients who have been virologically suppressed (viral load <50 copies/mL) for at least six months with no history of treatment failure.
Med Lett Drugs Ther. 2016 May 9;58(1494):60-1 |  Show IntroductionHide Introduction

Tenofovir Alafenamide (Vemlidy) for Hepatitis B

   
The Medical Letter on Drugs and Therapeutics • Jan 02, 2017  (Issue 1511)
Hepsera (Gilead) 1238.20 Emtricitabine – Emtriva (Gilead) 200 mg caps; 10 mg/mL oral soln 200 mg PO once ...
The FDA has approved tenofovir alafenamide (Vemlidy – Gilead) for treatment of chronic hepatitis B virus (HBV) infection in adults with compensated liver disease. It is the first single-drug product containing tenofovir alafenamide (TAF), a prodrug of the nucleotide reverse transcriptase inhibitor tenofovir, to become available; several combination products containing TAF are approved for treatment of HIV-1 infection. Tenofovir disoproxil fumarate (TDF; Viread – Gilead), another tenofovir prodrug, has been used for many years for treatment of chronic HBV infection; a generic...
Med Lett Drugs Ther. 2017 Jan 2;59(1511):6-8 |  Show IntroductionHide Introduction

Intravenous Ciprofloxacin

   
The Medical Letter on Drugs and Therapeutics • Aug 09, 1991  (Issue 850)
’’ comparable to a 500-mg oral dose. A 200-mg IV dose is equivalent to a 250-mg oral dose. After IV ...
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 IntroductionHide Introduction

Loracarbef

   
The Medical Letter on Drugs and Therapeutics • Sep 18, 1992  (Issue 879)
be allergic to loracarbef. DOSAGE — The recommended dosage of loracarbef is 200 to 400 mg q12h for adults ...
Loracarbef (Lorabid - Lilly), a new beta-lactam antibiotic with antimicrobial activity similar to the second-generation cephalosporins, has been approved by the US Food and Drug Administration for treatment of respiratory, skin, and urinary tract infection caused by susceptible organisms in both adults and children. It will probably compete with drugs such as trimethoprim-sulfamethoxazole (Bactrim, Septra, and others), amoxicillin-clavulanic acid (Augmentin), cefaclor (Ceclor), cefuroxime axetil (Ceftin), and cefprozil (Cefzil - Medical Letter, 34:63,...
Med Lett Drugs Ther. 1992 Sep 18;34(879):87-8 |  Show IntroductionHide Introduction

Eplerenone (Inspra)

   
The Medical Letter on Drugs and Therapeutics • May 12, 2003  (Issue 1156)
with mild to moderate hypertension in South Africa and the US compared eplerenone 50-200 mg/day ...
Eplerenone (e pler' en one; Inspra - Pharmacia), an aldosterone receptor antagonist similar to spironolactone (Aldactone, and others), has been approved by the FDA, but not yet marketed, for treatment of hypertension. It has also been tried for treatment of heart failure.
Med Lett Drugs Ther. 2003 May 12;45(1156):39-40 |  Show IntroductionHide Introduction