Search Results for "Depression"
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Searched for Depression. Results 51 to 60 of 379 total matches.
Fluoxetine (Prozac) Revisited
The Medical Letter on Drugs and Therapeutics • Sep 07, 1990 (Issue 826)
and should take lower
doses.
EFFECTIVENESS — Depression − Fluoxetine has proven to be about as effective ...
In the short time since fluoxetine (Prozac - Lilly) first became available in the USA (Medical Letter, 30:45, 1988), it has become the most frequently prescribed of all antidepressants. Some recent reports, however, have questioned its safety.
Venlafaxine - A New Antidepressant
The Medical Letter on Drugs and Therapeutics • Jun 10, 1994 (Issue 924)
) was recently approved by the US Food
and Drug Administration for treatment of depression. An aminomethyl ...
Venlafaxine hydrochloride (Effexor - Wyeth-Ayerst) was recently approved by the US Food and Drug Administration for treatment of depression. An aminomethyl-benzyl- cyclohexanol, it is chemically related to bupropion (Wellbutrin).
Mirtazapine - A New Antidepressant
The Medical Letter on Drugs and Therapeutics • Dec 20, 1996 (Issue 990)
) has been approved by the US Food and
Drug Administration for treatment of depression. A tetracyclic ...
Mirtazapine (mir taz a peen; Remeron - Organon) has been approved by the US Food and Drug Administration for treatment of depression. A tetracyclic piperazinoazepine, it is an analog of mianserin, an antidepressant available in Europe, but is structurally unrelated to antidepressants previously available in the USA.
Are SSRIs Safe for Children?
The Medical Letter on Drugs and Therapeutics • Jul 07, 2003 (Issue 1160)
paroxetine (Paxil in the US; Seroxat in the
UK) to treat children and adolescents with depression ...
A "Dear Colleague" letter from the UK's Committee on Safety of Medicines advised physicians, on the basis of unpublished data, not to use paroxetine (Paxil in the US; Seroxat in the UK) to treat children and adolescents with depression because of possible increased risk of suicidal behavior. This review describes the efficacy and safety of SSRIs in children.
Nalmefene - Long-Acting Injectable Opioid Antagonist
The Medical Letter on Drugs and Therapeutics • Oct 27, 1995 (Issue 960)
depression, sedation and hypotension and for management of known or suspected opioid overdose ...
Nalmefene (Revex - Ohmeda), an i methylene analog of naltrexone (Trexan), is a long-acting opioid antagonist that has been approved by the US Food and Drug Administration for reversal of postoperative opioid drug effects, including respiratory depression, sedation and hypotension and for management of known or suspected opioid overdose in the emergency department. The only other opioid antagonists available in the USA are naloxone (Narcan), which is also injectable but has a short duration of action, and naltrexone, which has a long duration of action but is marketed only for oral...
Risks of Tramadol and Gabapentin Use for Pain
The Medical Letter on Drugs and Therapeutics • Feb 02, 2026 (Issue 1747)
, constipation, and respiratory depression.
The FDA has restricted the use of tramadol in children ...
Tramadol (Ultram, and others) and gabapentin
(Neurontin, and others) are increasingly being
prescribed for treatment of chronic pain despite reports
of serious adverse events associated with their use.
Both drugs are touted as safer and less addictive than
strong opioids, but supporting evidence is lacking.
Med Lett Drugs Ther. 2026 Feb 2;68(1747):22-4 doi:10.58347/tml.2026.1747d | Show Introduction Hide Introduction
In Brief: Khedezla - A New Brand of Desvenlafaxine
The Medical Letter on Drugs and Therapeutics • Jan 06, 2014 (Issue 1433)
) desvenlafaxine
(Khedezla – Par/Osmotica) for treatment of depression.
It is the third extended-release ...
The FDA has approved the marketing of another extended-release brand-name formulation of the serotonin and norepinephrine reuptake inhibitor (SNRI) desvenlafaxine (Khedezla – Par/Osmotica) for treatment of depression. It is the third extended-release formulation of desvenlafaxine to become available in the US. Khedezla was approved using a 505(b)(2) application, a new drug application (NDA) that relies upon the FDA's findings of safety and/or effectiveness for a previously approved drug.Khedezla does not appear to offer any advantage over the other extended-release formulations of...
Duloxetine (Cymbalta) for Fibromyalgia
The Medical Letter on Drugs and Therapeutics • Jul 28, 2008 (Issue 1291)
and norepinephrine
reuptake inhibitor (SNRI) that is already marketed for
treatment of depression and diabetic ...
Duloxetine (Cymbalta - Lilly) is the second drug to be approved by the FDA for treatment of fibromyalgia. Pregabalin (Lyrica), which is also approved for treatment of neuropathic pain and epilepsy, was the first. Duloxetine is a selective serotonin and norepinephrine reuptake inhibitor (SNRI) that is already marketed for treatment of depression and diabetic neuropathy.
Flibanserin (Addyi) for Hypoactive Sexual Desire Disorder
The Medical Letter on Drugs and Therapeutics • Sep 28, 2015 (Issue 1478)
with other
CNS depressants, such as opioids or hypnotics, could
increase the risk of CNS depression.
Concurrent ...
The FDA has approved flibanserin (Addyi – Sprout) for
treatment of premenopausal women with acquired,
generalized hypoactive sexual desire disorder
(HSDD) not caused by another medical or psychiatric
condition, the effects of another drug, or relationship
difficulties. Flibanserin is the first drug to be approved
for treatment of HSDD. It is not approved for use
in men or postmenopausal women. Previous FDA
reviews of flibanserin in 2010 and 2013 did not result
in approval.
Oral Transmucosal Fentanyl Citrate
The Medical Letter on Drugs and Therapeutics • Mar 18, 1994 (Issue 918)
be given
orally and does not cause respiratory depression, but may make children unarousable, with a risk ...
Fentanyl, a synthetic opioid previously available for parenteral use in anesthesia (Sublimaze, and others) and in a transdermal patch for chronic pain (Duragesic - Medical Letter, 34:97, 1992), has now also been marketed as a raspberry-colored lozenge on a plastic handle (Fentanyl Oralet - Abbott), which resembles a lollipop. The new formulation will probably be promoted mainly for premedication of children before anesthesia, but has also been approved by the US Food and Drug Administration (FDA) for preanesthetic use in adults and for use in anesthesia or 'monitored anesthesia care' in...
