Search Results for "establish"
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Searched for establish. Results 91 to 100 of 654 total matches.
New Recommendation for Immunization Against Pertussis and Hepatitis B
The Medical Letter on Drugs and Therapeutics • Jul 24, 1992 (Issue 875)
the pertussis
component, but a cause-and-effect relationship has never been established (GS Golden, J Pediatr ...
The Immunization Practices Advisory Committee of the US Public Health Service now recommends immunizing all infants and some adolescents against hepatitis B and using a new diphtheria-tetanus-acellular pertussis vaccine (DTaP; ACEL-IMUNE - Lederle) for the fourth and fifth doses of DTP, usually given at 15 to 18 months of age and before school entry (Morbid Mortal Weekly Rep, 40 RR-13:1, November 22, 1991; Morbid Mortal Weekly Rep, 41 RR-1:1, Feb 7, 1992). The Committee on Infectious Diseases of the American Academy of Pediatrics has made similar recommendations but would extend...
Carvedilol for Heart Failure
The Medical Letter on Drugs and Therapeutics • Sep 26, 1997 (Issue 1010)
in patients with heart failure remains to be established (M Packer et al, N Engl J Med, 334:1349, 1996;
LA ...
Carvedilol (Coreg - SmithKline Beecham and Boehringer-Mannheim), a betaadrenergic and alpha-adrenergic blocker approved by the FDA for treatment of hypertension in 1995, but not marketed at that time, has now been approved and marketed for treatment of mild or moderate (NYHA class II or III) heart failure stabilized on other drugs. It is being promoted as an add-on drug that reduces the morbidity and mortality of the disease.
Nateglinide For Type 2 Diabetes
The Medical Letter on Drugs and Therapeutics • Apr 02, 2001 (Issue 1101)
has not
been established.
30 The Medical Letter • Vol. 43 (Issue 1101) April 2, 2001
DOSAGE — Starlix is available as 60 ...
Nateglinide (Starlix), a new meglitinide oral glucose-lowering agent, has been approved by the FDA.
Insulin Glargine (Lantus), A New Long-acting Insulin
The Medical Letter on Drugs and Therapeutics • Aug 06, 2001 (Issue 1110)
to be established. One study reported a higher affinity than native insulin for the insulin-like growth factor (IGF ...
Insulin Glargine (Lantus) is a new long-acting human insulin analog approved by the FDA for treatment of both type 1 and type 2 diabetes. Synthesized by recombinant DNA technology, it differs from human insulin at position 21 in the A-chain where asparagine is replaced by glycine and at the C-terminus of the B-chain where two arginines are added.
Buprenorphine: An alternative to Methadone
The Medical Letter on Drugs and Therapeutics • Feb 17, 2003 (Issue 1150)
has been established in randomized controlled trials (L Gowing et al, Cochrane Database Syst
EDITOR: Mark Abramowicz ...
The FDA has approved the marketing of buprenorphine in sublingual tablets (Reckitt Benckiser) both alone (Subutex) and with naloxone (Suboxone) for treatment of opioid dependence. Previously available only for parenteral use in treatment of pain (Buprenex, and others), it offers an alternative to methadone (Dolophine, and others), which is now often abused (New York Times, February 9, 2003; page 1). As a schedule III narcotic, buprenorphine will be subject to fewer prescribing restrictions than a schedule II drug such as methadone (MJ Kreek and FJ Vocci, J Subst Abuse Treat 2002;...
L-Carnitine
The Medical Letter on Drugs and Therapeutics • Nov 22, 2004 (Issue 1196)
-established indication, and that is for treatment
of carnitine deficiency. In clinical trials, the drug also ...
Carnitine is a naturally occurring amino acid derivative essential for transport of long-chain fatty acids into mitochondria. It is advertised on the Internet as a dietary supplement that can promote weight loss, increase energy, enhance athletic performance and slow aging. Levocarnitine (Carnitor - Sigma-Tau) has been FDA approved for oral and parenteral treatment of primary carnitine deficiency since 1986. Products containing levocarnitine and its synthetic derivative acetyl-L-carnitine are available as dietary supplements in the US.
ARBs and Myocardial Infarction
The Medical Letter on Drugs and Therapeutics • May 09, 2005 (Issue 1208)
they lower blood pressure without inducing a cough. It
has not been established that they provide the same ...
Angiotensin receptor blockers (ARBs) are widely used as an alternative to angiotensin converting enzyme (ACE) inhibitors for treatment of hypertension because they lower blood pressure without inducing a cough. It has not been established that they provide the same cardiac benefits as ACE inhibitors. Recently, an editorial in the British Medical Journal suggested that ARBs may increase the risk of myocardial infarction.
Rifaximin (Xifaxan) for Irritable Bowel Syndrome with Diarrhea
The Medical Letter on Drugs and Therapeutics • Aug 03, 2015 (Issue 1474)
could
lead to bacterial resistance remains to be established.
PREGNANCY — Teratogenic effects occurred ...
Rifaximin (Xifaxan – Salix), a minimally absorbed
oral antibiotic approved previously to treat travelers'
diarrhea and to reduce the risk of recurrent hepatic
encephalopathy, has now been approved by the FDA
for treatment of irritable bowel syndrome with diarrhea
(IBS-D). Eluxadoline (Viberzi – Actavis), a mu-opioid
receptor agonist, was also recently approved for IBS-D
and will be reviewed in a future issue.
Empagliflozin/Metformin (Synjardy) for Type 2 Diabetes
The Medical Letter on Drugs and Therapeutics • Dec 21, 2015 (Issue 1484)
,
double-blind trial in 7020 patients with type 2
diabetes and established cardiovascular disease (prior ...
The FDA has approved Synjardy (Boehringer Ingelheim/Lilly), a fixed-dose combination of the sodium-glucose
co-transporter 2 (SGLT2) inhibitor empagliflozin
(Jardiance) and metformin (Glucophage, and others),
for treatment of patients with type 2 diabetes not
adequately controlled on either of these drugs alone
or already being treated with both empagliflozin and
metformin. It is the third SGLT2 inhibitor/metformin
combination to be approved in the US.
Dupilumab (Dupixent) for Moderate to Severe Atopic Dermatitis
The Medical Letter on Drugs and Therapeutics • Apr 24, 2017 (Issue 1519)
has not been established.
The FDA recently approved crisaborole 2% ointment
(Eucrisa), a topical phosphodiesterase type-4 ...
The FDA has approved dupilumab (Dupixent – Sanofi/Regeneron), a subcutaneously-injected fully human
monoclonal antibody, for treatment of adults with
moderate to severe atopic dermatitis (eczema) that
has not responded to topical therapies. It can be used
with or without topical corticosteroids.