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Searched for days. Results 1831 to 1840 of 1856 total matches.
Odefsey - Another NNRTI Combination for HIV
The Medical Letter on Drugs and Therapeutics • May 09, 2016 (Issue 1494)
disoproxil fumarate; TAF = tenofovir alafenamide
1. Approximate WAC for 30 days’ treatment. WAC = wholesaler ...
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.
Glycopyrrolate/Formoterol (Bevespi Aerosphere) for COPD
The Medical Letter on Drugs and Therapeutics • Oct 10, 2016 (Issue 1505)
= inhalation spray inhaler; MDI = metered-dose inhaler; soln = solution
1. Approximate WAC for 30 days ...
The FDA has approved a fixed-dose combination of
the long-acting anticholinergic glycopyrrolate and
the long-acting beta2-adrenergic agonist (LABA)
formoterol (Bevespi Aerosphere – AstraZeneca) for
long-term maintenance treatment of patients with
chronic obstructive pulmonary disease (COPD).
Glycopyrrolate/formoterol is the fourth long-acting
anticholinergic/LABA combination to be approved in
the US, but the first to become available in a metered-dose
inhaler. Glycopyrrolate/indacaterol (Utibron
Neohaler), umeclidinium/vilanterol (Anoro Ellipta),
and tiotropium/olodaterol (Stiolto...
Risankizumab (Skyrizi) - An IL-23 Antagonist for Crohn's Disease
The Medical Letter on Drugs and Therapeutics • Dec 26, 2022 (Issue 1666)
days (in patients with Crohn’s disease)
Table 2. Risankizumab Clinical Trial Results
Clinical ...
The injectable interleukin (IL)-23 antagonist
risankizumab-rzaa (Skyrizi – Abbvie) has been
approved by the FDA for treatment of moderately
to severely active Crohn's disease (CD) in adults.
Risankizumab was approved earlier for treatment of
plaque psoriasis and psoriatic arthritis.
Antimicrobial Prophylaxis for Surgery
The Medical Letter on Drugs and Therapeutics • May 23, 2016 (Issue 1495)
of metronidazole
at 7 PM and 11 PM the day before an 8 AM operation.
intraoperative continuous-infusion cefazolin ...
Antimicrobial prophylaxis can decrease the
incidence of postoperative surgical site infection
after some procedures. Since the last Medical Letter
article on this subject, consensus guidelines have
been published. Recommendations for prophylaxis
in specific surgical procedures are listed in Table 1.
Cholesterol Rethink for High-Risk Patients
The Medical Letter on Drugs and Therapeutics • May 10, 2004 (Issue 1182)
for 30 days' treatment, according to the most recent data (March 31, 2004) from retail pharmacies ...
The recent "PROVE IT" trial in patients with coronary heart disease showed clinical benefits associated with reducing LDL cholesterol concentrations lower than the 100 mg/dL (2.59 mmol/L) or less that had been considered optimal.
Pioglitazone/Metformin (Actoplus met)
The Medical Letter on Drugs and Therapeutics • Jan 30, 2006 (Issue 1227)
divided 126.00
1. Cost of 30 days’ supply at the highest daily dosage based on most recent
data ...
For patients with diabetes poorly controlled with a single oral drug, addition of a second drug with a different mechanism can be helpful. A fixed-dose combination (Actoplus met - Takeda) of two widely used antihyperglycemic drugs, the thiazolidinedione pioglitazone (Actos) and the biguanide metformin (Glucophage, and others), has been approved by the FDA for management of type 2 diabetes. It is indicated for patients already being treated with both pioglitazone and metformin or as second-line therapy for those not adequately controlled with either metformin or pioglitazone alone....
Inhaled Insulin (Exubera)
The Medical Letter on Drugs and Therapeutics • Jul 17, 2006 (Issue 1239)
be administered no earlier than 10 minutes before a meal. The wholesale
acquisition cost is $3.73-5.00 per day ...
An inhaled, dry-powder formulation of rapid-acting human insulin (Exubera - Pfizer) has been approved by the FDA for treatment of adults with type 1 or type 2 diabetes.
PARP Inhibitors for Ovarian Cancer
The Medical Letter on Drugs and Therapeutics • Dec 04, 2017 (Issue 1535)
impairment. All of these drugs can be taken with or without food.
3. Approximate WAC for 30 days’ treatment ...
Three oral poly(ADP-ribose) polymerase (PARP)
inhibitors have been approved by the FDA for treatment
of advanced, recurrent ovarian cancer. Olaparib
(Lynparza – AstraZeneca), niraparib (Zejula – Tesaro),
and rucaparib (Rubraca – Clovis) are each approved
for somewhat different indications and for patients
with different biomarkers (see Table 2).
Trelegy Ellipta - A Three-Drug Inhaler for COPD
The Medical Letter on Drugs and Therapeutics • May 21, 2018 (Issue 1547)
inhalation technique.
2. Approximate WAC for 30 days’ treatment at the lowest recommended adult dosage. WAC ...
The FDA has approved Trelegy Ellipta (GSK), a fixed-dose
combination of the inhaled corticosteroid (ICS)
fluticasone furoate, the long-acting antimuscarinic
agent (LAMA) umeclidinium, and the long-acting
beta2-agonist (LABA) vilanterol. It is available as a dry
powder inhaler for once-daily maintenance treatment
of COPD and to reduce COPD exacerbations in patients
with a history of exacerbations. Trelegy Ellipta is
the first three-drug inhaler for treatment of COPD to
become available in the US.
Biktarvy - Another INSTI-Based Combination for HIV
The Medical Letter on Drugs and Therapeutics • Aug 13, 2018 (Issue 1553)
3090.00
TAF = tenofovir alafenamide; TDF = tenofovir disoproxil fumarate
1. Approximate WAC for 30 days ...
The FDA has approved Biktarvy (Gilead), a once-daily,
fixed-dose combination of bictegravir, a new integrase
strand transfer inhibitor (INSTI), and the nucleoside
reverse transcriptase inhibitors (NRTIs) emtricitabine
and tenofovir alafenamide (TAF), for treatment of HIV-1
infection in adults. The new combination is indicated for
use in patients who are antiretroviral-naive or who have
been virologically suppressed on a stable antiretroviral
regimen for ≥3 months with no history of treatment
failure and no known substitutions associated with
resistance to any component of the...