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Searched for days. Results 1211 to 1220 of 1864 total matches.
Beta Interferons for Multiple Sclerosis
The Medical Letter on Drugs and Therapeutics • Oct 14, 2002 (Issue 1141)
every other day SC 13,104
1. Cost for one year’s treatment according to AWP listings in Drug Topics Red ...
Three beta interferons are widely used in the treatment of patients with relapsing-remitting multiple sclerosis (RRMS).
Anastrozole (Arimidex) vs. Tamoxifen for Treatment of Early Breast Cancer
The Medical Letter on Drugs and Therapeutics • Mar 17, 2003 (Issue 1152)
with tamoxifen.
DOSAGE AND COST — The dosage of anastrozole is 1 mg PO once daily. The cost of 30
days ...
Anastrozole (Arimidex - AstraZeneca, Medical Letter 1996; 38:61), an aromatase inhibitor, has received accelerated approval from the FDA for adjuvant treatment of postmenopausal women with early hormone-receptor-positive breast cancer. The drug was approved for treatment of postmenopausal women with metastatic breast cancer in 1996.
In Brief: New Propellants for Albuterol Metered-Dose Inhalers
The Medical Letter on Drugs and Therapeutics • Nov 03, 2008 (Issue 1298)
. December 31, 2008 will be
the last day that albuterol MDIs using CFC propellants
can be sold ...
Inhaled drugs for asthma are available in the US mainly in pressurized metered-dose inhalers (MDIs), which require a propellant, and dry powder inhalers, which do not. The chlorofluorocarbon (CFC) propellants in MDIs are being replaced by hydrofluoroalkane (HFA) propellants for environmental reasons: CFCs contribute to the depletion of the ozone layer. December 31, 2008 will be the last day that albuterol MDIs using CFC propellants can be sold in the US. The FDA is expected to announce a termination date for other CFC-containing products in the near future.Three HFA albuterol inhalers and one...
Belimumab (Benlysta) for Systemic Lupus Erythematosus
The Medical Letter on Drugs and Therapeutics • Jun 13, 2011 (Issue 1366)
are not recommended. Live vaccines
should not be administered within 30 days before
or during treatment ...
Belimumab (Benlysta – Human Genome Sciences/GlaxoSmithKline) has been approved by the FDA for
treatment of adults with active, autoantibody-positive, systemic lupus erythematosus (SLE). It is the first biologic
agent approved for SLE and the first drug of any kind to be approved for this disease in >50 years.
A Fixed-Dose Combination of Ibuprofen and Famotidine (Duexis)
The Medical Letter on Drugs and Therapeutics • Oct 31, 2011 (Issue 1376)
-day supply according to drugstore.com. Accessed October 21, 2011. Cost based on a daily dose ...
The FDA has approved Duexis (Horizon), a fixed-dose
combination of the nonsteroidal anti-inflammatory drug
(NSAID) ibuprofen and the H2-receptor antagonist
(H2RA) famotidine, for symptomatic relief of osteoarthritis
and rheumatoid arthritis and to decrease the risk of
developing gastric and duodenal ulcers in patients at
risk for NSAID-associated ulcers. Vimovo, a combination
of the NSAID naproxen and the proton pump
inhibitor (PPI) esomeprazole, is also approved by the
FDA for prevention of NSAID-associated gastric ulcers.
Lubiprostone (Amitiza) for Opioid-Induced Constipation
The Medical Letter on Drugs and Therapeutics • Jun 10, 2013 (Issue 1418)
)
Methylnaltrexone3 8 mg/0.4 mL, 8 or 12 mg SC 812.10
(Relistor – Salix) 12 mg/0.6 mL every other
solution in day ...
The FDA has approved use of lubiprostone (Amitiza)
for treatment of opioid-induced constipation in adults
with chronic non-cancer pain. The drug was previously
approved for chronic idiopathic constipation and irritable
bowel syndrome with constipation.
Apremilast (Otezla) for Psoriatic Arthritis
The Medical Letter on Drugs and Therapeutics • May 26, 2014 (Issue 1443)
effects, apremilast
should be titrated over 6 days from 10 mg twice daily
to a final recommended dosage ...
Apremilast (Otezla – Celgene), an oral phosphodiesterase
type-4 (PDE4) inhibitor, has been approved
by the FDA for treatment of active psoriatic arthritis in
adults. It is the fi rst PDE4 inhibitor to be approved for this
indication.
Afatinib (Gilotrif) for Advanced Non-Small Cell Lung Cancer (online only)
The Medical Letter on Drugs and Therapeutics • May 25, 2015 (Issue 1469)
or
to chemotherapy with cisplatin plus pemetrexed every
21 days for up to 6 cycles. Median progression-free ...
The FDA has approved afatinib (Gilotrif — Boehringer
Ingelheim), an oral epidermal growth factor receptor
(EGFR) tyrosine kinase inhibitor, for first-line treatment
of patients with metastatic non-small cell lung cancer
(NSCLC) whose tumors have EGFR exon 19 deletions
or exon 21 (L858R) substitution mutations. These
mutations occur in about 10% of patients with NSCLC.
Afatinib is the second EGFR inhibitor to be approved
for first-line treatment of advanced lung cancer. The
first was erlotinib (Tarceva), which is also approved
for treatment of patients with locally advanced...
Which PPI?
The Medical Letter on Drugs and Therapeutics • Jun 22, 2015 (Issue 1471)
pylori infection.
2. PPIs are generally taken 30-60 minutes before the first meal of the day. Taking one ...
An article published in the New York Times on May 1,
2015 listed the 10 drugs on which Medicare Part D
spent the most in 2013. The most costly ($2.53
billion) was the proton pump inhibitor (PPI) Nexium
(esomeprazole magnesium), which has recently become
available generically.
A Recombinant C1 Esterase Inhibitor (Ruconest) for Hereditary Angioedema (online only)
The Medical Letter on Drugs and Therapeutics • Mar 28, 2016 (Issue 1491)
lasting 2-5 days, typically involving the
extremities, gastrointestinal tract, genitalia, face ...
The FDA has approved Ruconest (Salix), a recombinant
analog of human complement component 1 esterase
inhibitor (C1INH), for treatment of acute attacks in
patients with hereditary angioedema (HAE).