PharmExec

AUGUST 7, 2025

Image Credit: Adobe Stock Images/Muhammed Topline Findings FDA approval milestone : Modeyso (dordaviprone) is the first and only treatment approved for recurrent H3 K27M-mutant diffuse midline glioma in patients aged one year and older. 1,2 What does FDA Approval of Modeyso mean for Patients with H3 K27M-Mutant Diffuse Midline Glioma?

FDA

The Checkup by Singlecare

DECEMBER 2, 2024

Two popularly prescribed medications for this use, as well as other conditions that cause pain, inflammation, and muscle spasms, are cyclobenzaprine and meloxicam. Both drugs are approved by the Food and Drug Administration (FDA) but for different uses. Cyclobenzaprine is classified in a group of drugs called skeletal muscle relaxants.

Dosage

PharmExec

AUGUST 1, 2025

Related Videos Related Content Advertisement August 1st 2025 FDA Mandates Safety Alterations to Opioid Pain Medication Labels Nicholas Jacobus FDA mandates new opioid labeling to highlight long-term risks, aiming to combat addiction and improve patient safety in pain management. Subscribe Now!

Communication

PharmExec

AUGUST 6, 2025

Related Videos Related Content Advertisement August 6th 2025 FDA Approves Expanded Indication for Teva’s Ajovy in Pediatric Patients with Episodic Migraine Don Tracy, Associate Editor August 6th 2025 Tariffs and Drug Prices: Understanding the Impact on Pharmaceuticals Miranda Schmalfuhs August 6th 2025 FDA Grants Priority Review to Bristol Myers Squibb’s (..)

Communication

PharmExec

AUGUST 6, 2025

The announcement coincides with leadership changes and controversies at HHS, including the resignation of FDA CBER Head Vinay Prasad amidst political pressure. In late July, FDA CBER Head Vinay Prasad announced he was stepping down from the role. SHOW MORE The move comes amidst a turbulent time at HHS. August 5, 2025.

Vaccines

The Checkup by Singlecare

MARCH 12, 2024

While browsing the aisles in a drug store or shopping online for pain relief, you will likely be inundated with many different brands and medication types. If you see medications labeled “Advil” and others labeled “ibuprofen,” you may ask yourself: “Is Advil the same as ibuprofen?”

Labelling

The Checkup by Singlecare

FEBRUARY 8, 2024

Food and Drug Administration (FDA) advisory committee met to discuss evidence suggesting that oral phenylephrine, one of the active ingredients found in most over-the-counter decongestants, is ineffective for relieving nasal congestion. However, the FDA has not yet arrived at a definite conclusion as the evidence is still under review.

Medication Labelling

The Checkup by Singlecare

JANUARY 4, 2024

In addition, the FDA label for the nighttime forms of Mucinex containing acetaminophen recommends avoiding three or more drinks per day. If you’ve already taken Mucinex, it’s recommended to wait until the medication’s effects clear from your system before consuming alcohol.

Immunization

The Checkup by Singlecare

AUGUST 1, 2023

Always read the medication label and, if you’re unsure, ask your child’s physician or pharmacist. Age appropriateness Tylenol OTC dosing is FDA-approved at age 2 while Motrin OTC dosing begins at 6 months old. Once a child is old enough to take the medication, calculate their dose based on their current weight.

Dosage

The Checkup by Singlecare

JULY 17, 2023

Food Drug Administration (FDA) , a generic medicine works in the same way and provides the same clinical benefit as brand-name medicine. Generic medications must have the same dosage form, safety, strength, route of administration, quality, performance characteristics, and intended use. According to the U.S.

Department of Veterans Affairs

The Checkup by Singlecare

NOVEMBER 19, 2024

Fluconazole is a prescription antifungal medication. It is approved by the Food and Drug Administration (FDA) to treat types of various fungal infections , such as vaginal yeast infections —where it is commonly taken as either a single dose or repeated doses. Fluconazole is often referred to by the brand name Diflucan.

Medication Labelling

PharmTech

AUGUST 1, 2025

Required labeling updates include clearer risk information, stronger warnings, and guidance on opioid use, with a 30-day submission deadline for manufacturers. The FDA recommends classifying 7-hydroxymitragynine products under the Controlled Substance Act due to abuse potential, affecting kratom-based therapeutic development.

Medication Labelling

The Checkup by Singlecare

JULY 14, 2023

Food and Drug Administration (FDA) recommends keeping your caffeine limit to 400 mg daily, or four to five cups of coffee (an 8-ounce cup of coffee contains 80-100 mg of caffeine). Nevertheless, the U.S. However, she adds that the literature is not clear on long-term effects of caffeine on the general inflammatory state.

Adverse Reactions

OctariusRx

MAY 15, 2023

In this post we discuss our most recent medication calculation quiz and how it can be used as a component to increase patient safety and enhance regulatory compliance. Food and Drug Administration (FDA) receives more than 100,000 reports associated with a suspected medication error. Each year, the U.S.

Long-Term Care Facilities

OctariusRx

MAY 13, 2024

In this post we discuss our most recent medication calculation quiz and how it can be used as a component to increase patient safety and enhance regulatory compliance. Food and Drug Administration (FDA) receives more than 100,000 reports associated with a suspected medication error. Each year, the U.S.

Long-Term Care Facilities

The Checkup by Singlecare

DECEMBER 1, 2022

Diclofenac is approved by the United States Food and Drug Administration (FDA) and is available by prescription only, although topical diclofenac is now available both by prescription and over-0the-counter. This is the strongest warning required by the FDA. How to take diclofenac. Take or use diclofenac exactly as prescribed.

Dosage