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Searched for action. Results 571 to 580 of 1170 total matches.
Axitinib (Inlyta) for Advanced Renal Cell Carcinoma
The Medical Letter on Drugs and Therapeutics • Jun 11, 2012 (Issue 1392)
inhibitor
Mechanism of action Inhibits VEGF receptors 1, 2 and 3
Formulation 1-mg and 5-mg tablets
Route ...
Axitinib (Inlyta – Pfizer), an oral tyrosine kinase
inhibitor, has been approved by the FDA for treatment
of advanced renal cell carcinoma after failure of one
prior systemic therapy. It is the fourth oral tyrosine
kinase inhibitor to be approved for treatment of
advanced renal cell carcinoma.
Vismodegib (Erivedge) for Basal Cell Carcinoma
The Medical Letter on Drugs and Therapeutics • Jul 09, 2012 (Issue 1394)
OF ACTION — The Hh signaling pathway,
which is important in embryonic development and
regulation of adult ...
The FDA has approved vismodegib (vis moe deg´ ib;
Erivedge – Genentech), the first hedgehog (Hh) pathway
inhibitor, for oral treatment of metastatic basal cell
cancer, locally advanced basal cell carcinoma that has
recurred after surgery, or locally advanced basal cell
carcinoma in adults who are not candidates for surgery
or radiation.
Ivermectin (Sklice) Topical Lotion for Head Lice
The Medical Letter on Drugs and Therapeutics • Aug 06, 2012 (Issue 1396)
Dermatol 2004; 21:670).
MECHANISM OF ACTION — Ivermectin is derived
from the fermentation of Streptomyces ...
The FDA has approved the antiparasitic drug ivermectin
in a 0.5% lotion (Sklice – Sanofi Pasteur) as a
single-use topical treatment for head lice in patients ≥6
months old. Oral ivermectin (Stromectol – Merck) is
effective for treatment of head lice resistant to other
therapies, but it has not been approved by the FDA for
this indication.
Raxibacumab for Anthrax
The Medical Letter on Drugs and Therapeutics • Apr 01, 2013 (Issue 1413)
, fever and myalgia.2
MECHANISM OF ACTION — Actively dividing
Bacillus anthracis produces protective ...
The FDA has approved raxibacumab (rax” ee bak’ ue
mab; GSK), a fully human monoclonal antibody given by
intravenous infusion, for treatment of inhalational anthrax
in combination with appropriate antibacterial drugs, and
for prophylaxis of inhalational anthrax when alternative
therapies are not available or are not appropriate. It was
approved under the Animal Efficacy Rule, which allows
the FDA to approve drugs that demonstrate efficacy in
animals, providing that they would have a reasonable
human health benefit and are safe for human use.
Raxibacumab is only available from the...
Icosapent Ethyl (Vascepa) for Severe Hypertriglyceridemia
The Medical Letter on Drugs and Therapeutics • Apr 29, 2013 (Issue 1415)
by 20-50%.3
MECHANISM OF ACTION — Omega-3 PUFAs
decrease hepatic production of triglycerides ...
Icosapent ethyl (Vascepa [vas EE puh] – Amarin), the
ethyl ester of eicosapentaenoic acid (EPA), has been
approved by the FDA as an adjunct to diet for treatment of
severe hypertriglyceridemia (≥500 mg/dL). Vascepa is
the second omega-3 polyunsaturated fatty acid (PUFA)
product to become available by prescription for this indication;
Lovaza (formerly Omacor), which is a combination
of the ethyl esters of EPA and docosahexaenoic acid
(DHA), was the first. Many omega-3 PUFA-containing
fish oil capsules are sold over the counter as dietary supplements.
Pasireotide (Signifor) for Cushing's Disease
The Medical Letter on Drugs and Therapeutics • May 13, 2013 (Issue 1416)
MECHANISM OF ACTION — Pasireotide is a somatostatin
analog with high binding affinity for human ...
The FDA has approved the somatostatin analog
pasireotide diaspartate (Signifor – Novartis) for treatment
of adults with Cushing's disease (cortisol excess caused
by an ACTH-secreting pituitary tumor) who are not candidates
for pituitary surgery or for whom surgery has not
been curative. Pasireotide is the first drug approved in
the US specifically to treat Cushing's disease. The
antiprogestin mifepristone (Korlym) was approved last
year for control of hyperglycemia in patients with
Cushing's syndrome, which includes other causes of
hypercortisolism, such as exogenous steroids and...
Lubiprostone (Amitiza) for Opioid-Induced Constipation
The Medical Letter on Drugs and Therapeutics • Jun 10, 2013 (Issue 1418)
of post-operative ileus.5
MECHANISM OF ACTION — Exogenous opioids
decrease peristalsis and secretion ...
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.
Tasimelteon (Hetlioz) for Non-24-Hour Sleep-Wake Disorder
The Medical Letter on Drugs and Therapeutics • Apr 28, 2014 (Issue 1441)
in the treatment of non-24, with some
success.3
MECHANISM OF ACTION — Melatonin acts on
two receptors ...
The FDA has approved the melatonin receptor agonist
tasimelteon (Hetlioz – Vanda) for treatment of non-24-hour sleep-wake disorder (non-24), which is common
in totally blind persons. Tasimelteon is the first drug
approved for this indication and the second melatonin
receptor agonist approved for use in the US; ramelteon
(Rozerem) was approved earlier for treatment of
insomnia. Melatonin itself has not been approved by
the FDA for any indication; it is available in the US as a
dietary supplement and is promoted as a sleep aid.
Apremilast (Otezla) for Psoriatic Arthritis
The Medical Letter on Drugs and Therapeutics • May 26, 2014 (Issue 1443)
inhibitors remains to be determined.3
MECHANISM OF ACTION — PDE4 degrades cyclic
adenosine monophosphate ...
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.
Eslicarbazepine Acetate (Aptiom) for Epilepsy
The Medical Letter on Drugs and Therapeutics • May 26, 2014 (Issue 1443)
to eslicarbazepine, the major
active metabolite
Elimination Urine
MECHANISM OF ACTION — As with oxcarbazepine ...
Eslicarbazepine acetate (Aptiom – Sunovion) has been
approved by the FDA for adjunctive treatment of partial-onset
seizures in adults. New drugs for epilepsy are
often approved by the FDA initially only as adjunctive
treatment for partial seizures. Eslicarbazepine acetate
is a prodrug of eslicarbazepine, which is the S-isomer of
the active metabolite of oxcarbazepine. Oxcarbazepine
itself is similar to carbamazepine. Both oxcarbazepine
and carbamazepine are available generically.