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Searched for insulin, regular. Results 1 to 4 of 4 total matches.
Insulins for Type 2 Diabetes
The Medical Letter on Drugs and Therapeutics • Dec 08, 2025 (Issue 1743)
or degludec) is slightly less likely than NPH insulin to cause
hypoglycemia.
▶ Mealtime use of regular ...
The goal of pharmacologic treatment for type 2
diabetes is to achieve and maintain a near-normal
glycated hemoglobin (A1C) concentration while
minimizing hypoglycemia; an A1C goal of <7%
is recommended for most patients to prevent or
reduce the microvascular complications of diabetes
(retinopathy, nephropathy, neuropathy). An A1C target
of <8% may be appropriate for patients who are older,
have comorbid conditions, or are at risk for serious
hypoglycemia-associated adverse events.
Med Lett Drugs Ther. 2025 Dec 8;67(1743):196-9 doi:10.58347/tml.2025.1743c | Show Introduction Hide Introduction
Comparison Chart: Some Available Insulins for Type 2 Diabetes (online only)
The Medical Letter on Drugs and Therapeutics • Dec 08, 2025 (Issue 1743)
of even number of units
Prandial Insulins
Regular Human Insulin
Humulin R (Lilly)
Novolin R ...
View the Comparison Chart: Some Available Insulins for Type 2 Diabetes
Med Lett Drugs Ther. 2025 Dec 8;67(1743):e201-4 doi:10.58347/tml.2025.1743d | Show Introduction Hide Introduction
Tirzepatide (Mounjaro) for Type 2 Diabetes
The Medical Letter on Drugs and Therapeutics • Jul 11, 2022 (Issue 1654)
at GIP and GLP-1 receptors, tirzepatide increases
insulin secretion, decreases glucagon secretion ...
The FDA has approved tirzepatide (Mounjaro –
Lilly), a peptide hormone with activity at both
glucose-dependent insulinotropic polypeptide
(GIP) and glucagon-like peptide-1 (GLP-1)
receptors, to improve glycemic control in adults
with type 2 diabetes. Tirzepatide, which is injected
subcutaneously once weekly, is the first dual GIP/GLP-1 receptor agonist to become available in the
US. Selective GIP receptor agonists are not available
in the US; GLP-1 receptor agonists have been
available for years.
Lonapegsomatropin (Skytrofa) for Growth Hormone Deficiency
The Medical Letter on Drugs and Therapeutics • Feb 07, 2022 (Issue 1643)
The Medical Letter ® Vol. 64 (1643) February 7, 2022
21
regularly in all patients. Increases in serum ...
Lonapegsomatropin-tcgd (Skytrofa – Ascendis), a long-acting prodrug of recombinant human growth hormone (rhGH), has been approved by the FDA for
once-weekly subcutaneous (SC) treatment of growth
failure due to inadequate secretion of endogenous
growth hormone in children ≥1 year old who weigh
≥11.5 kg. It is the first once-weekly rhGH product to be
approved in the US; other available rhGH formulations
are administered more frequently.
