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2 Pharmacists can play a large role in the management of IBD, especially because medication nonadherence is common, leading to increased flares, hospitalizations, and complications. Disease management—such as medication, surgery, and diet—was prevalent in 32% of videos.
Additionally, gabapentin is typically used as a human medicine; its prescribed off-label for dogs since it doesnt have FDA approval for them yet. What is the maximum dosage for gabapentin in dogs The maximum dose of gabapentin for dogs is 30 mg/kg. She urges dog parents to get dosage approval by their prescribing veterinarian.
Importantly, Novavax received FDA approval in May 2025 with restrictions: It is approved for individuals 65 years and older and patients aged 12 to 64 years with at least 1 health condition that puts them at risk for severe COVID-19. link] Seasonal influenza vaccine dosage & administration. October 16, 2024. Accessed May 29, 2025.
By incorporating a patient's genetic profile into therapeutic decision-making, pharmacists can identify optimal drug choices and dosages while minimizing the risk of adverse events (AEs). This is particularly vital in polypharmacy scenarios, where the risk of drug-drug interactions and cumulative toxicity is high.
Its not safe or effective, according to the Food and Drug Administration (FDA), and it may lead to serious health problems. Although these medications are effective, the FDA has not yet approved generic versions, meaning people can only get a prescription for semaglutide under its brand name. Is compounded semaglutide safe?
Over 40 new medications have been approved by the FDA, giving patients more options for treating various health problems. Zelsuvmi (berdazimer) Zelsuvmi received the green light from the FDA on January 5, 2024. Zelsuvmi’s approval is a big deal because it’s only the second FDA-approved treatment for this condition.
That is, they have the same active ingredients, FDA-approved uses, and dosages administered with a prefilled pen. They are administered via once-daily subcutaneous injections and prescribed at the same dosage of 20 micrograms (mcg). Teriparatide vs. Forteo: Is there a difference? Generic and brand-name Forteo are biosimilar.
Food and Drug Administration (FDA) to manage Type 2 diabetes mellitus. Oral tablet: 5 mg, 10 mg Oral tablet: 10 mg, 25 mg What is the standard dosage? For heart failure hospitalization, those on Farxiga had a higher risk than those on Jardiance, particularly at the lower 5 mg dose of Farxiga.
Food & Drug Administration (FDA) to treat generalized anxiety disorder. It can help with sleep troubles in certain individuals—although the typical dosage varies. Buspirone does not have a sedating effect, according to Raj Dasgupta, MD , sleep specialist and program director at Huntington Health Hospital in California.
Ozempic is the brand name for semaglutide, which is a medication thats FDA approved to treat high blood sugar in people with Type 2 diabetes. I would not change the dosage or stop a GLP1-RA in the setting of arrhythmias or palpitations, Dr. Hmoud says. Most people dont have this issue, but for those who do, it can feel unsettling.
SHOW MORE The FDA approved acalabrutinib as a frontline option for untreated mantle cell lymphoma. The FDA’s review of acalabrutinib was conducted under Project Orbis, an initiative of the FDA Oncology Center of Excellence that enables concurrent submission and review of oncology drugs across international regulatory agencies.
Selection of an appropriate OTC analgesic should take into consideration various patient factors, including the patient’s overall health status, current medical conditions, and medication profile, as well as patient preferences, which are often influenced by dosage form, required dosing intervals, and cost of OTC medication.
It will be interesting to see what dosage form these data prompt the future development of. It also introduces a question on how to optimize the PK/pharmacodynamic profile for protein degraders, such as cereblon E3 ligase modulatory drugs and proteolysis-targeting chimeras, which are a burgeoning area of therapeutic development.”
The Orange Book is the reference, and it allows the FDA to declare something [to be] therapeutically equivalent. The FDA Approval Process Within the FDA approval process, the 505(b)(1) new drug application (NDA) submission pathway is the pathway by which new drugs are able to seek approval.
Relapse risk factors include prior hospitalizations, long illness duration, and antipsychotic polypharmacy, emphasizing the need for effective maintenance treatments. Maintaining stability in schizophrenia is a major clinical challenge—each relapse can disrupt functioning, burden caregivers, and elevate hospitalization risk.
A group of experts will present an encore abstract titled " Prevalence of Dosage Modifications and Impact on Response Milestone Among Patients With CML Treated With Imatinib Using Real-World Data " at the 2025 Oncology Pharmacists Connect (OPC) meeting in Austin, Texas, from June 19 to 20.
SHOW MORE Real-world data shows patients switching from Humira to biosimilars Hadlima and Hyrimoz achieve similar outcomes without hospitalization. The study's primary objective was to assess reversion rates to Humira, with 9% reverting after three months, while 91% remained on biosimilars or switched to alternatives.
Image credit: Shutter2U | stock.adobe.com Biosimilars are biologic products highly similar to an FDA-approved reference product, with no clinically meaningful differences in safety, purity, or potency. Misconceptions can lead to unnecessary hesitation, increased health care spending, and reduced access to important biologic treatments.
Phenobarbital is FDA approved to prevent and treat several types of seizure disorders, including epilepsy and status epilepticus. Phenobarbital is a long-acting barbiturateits effect lasts up to 12 hours, and it can stay in your system for several days to weeks, depending on factors like dosage and individual metabolism.
FDA approval of LIMITX for broader use could significantly impact opioid misuse prevention and save lives. Or, as FDA officials like to call it, “multiple tablet ingestion”—I guess it sounds better to them. trillion economic impact in 2020. SHOW MORE A novel solution can strategically control the release of the drug in vivo.
Meloxicam injection (Xifyrm; Azurity Pharmaceuticals, Inc) received FDA approval for use in adults for the management of moderate-to-severe pain, either alone or in combination with non-steroidal anti-inflammatory drug (NSAID) analgesics.
Despite observational evidence, causation is not established, necessitating further research on dosage effects and neurocognitive outcomes. The study emphasizes the importance of pharmacist involvement in monitoring cognitive risks and managing long-term gabapentin therapy.
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2-4 In the United States, the FDA had approved 44 cell therapy products as of March 6, 2025. In October 2024, CAR T therapy axicabtagene ciloleucel (Yescarta; Kite Pharma) received FDA regenerative medicine advanced therapy designation as a first-line treatment for high-risk large B-cell lymphoma.
This international study is ongoing despite the recent FDA decision to reject MDMA-assisted therapy for PTSD, and it has the potential to add another treatment paradigm for patients with cancer. Potential Roles of the Oncology Pharmacist My friend died of his metastatic cancer in early 2025.
Limitations included open-label design and dosage constraints, but the multicountry approach enhanced generalizability and external validity. All patients underwent a 20-week correction period for dosage titration and Hb correction, which was followed by an 8-week evaluation for efficacy assessments.
1 A total of 80 women aged 45 and older who were starting treatment at the oncology outpatient clinic of the hospital at FMB-UNESP were included in the randomized clinical trial. 1,2 “Even with a small sample of participants, it was possible to observe a significant difference in the response to chemotherapy. P = 0.04).
Bristol Myers Squibb (BMS) has announced that the US Food and Drug Administration (FDA) has given approval to label updates for its CAR T cell therapies, Breyanzi (lisocabtagene maraleucel; liso-cel) and Abecma (idecabtagene vicleucel; ide-cel) to treat multiple myeloma. Credit: Saiful52 / Shutterstock. Sign up for our daily news round-up!
Food and Drug Administration (FDA) to help manage Type 2 diabetes, these drugs are now also widely prescribed for weight loss, weight management, and cardiovascular health. a clinical pharmacist with the University of Illinois Hospital and Health Sciences System. Originally approved by the U.S.
Buprenorphine is FDA approved for use in humans and cats , but not dogs. Most of the time, buprenorphine is administered by injection at your veterinary clinic or at an animal hospital, Krista Hight, DVM , veterinarian at Central Maui Animal Clinic at Thrive Pet Healthcare, explains. Usually, it’s determined on a case-by-case basis.
It’s common for medications to stay in your body for four half-lives, says Joyce Oen-Hsiao, MD, an associate professor of medicine at Yale School of Medicine and director of Cardiac Rehabilitation Services at Yale-New Haven Hospital Heart & Vascular Center. This means benazepril stays in the body longer at the same dosage.
Animal studies reveal dose-dependent hepatic responses to CBD, supporting the need for cautious monitoring even at consumer-relevant dosages. 2 Despite its widespread acceptance, an FDA-led clinical trial unexpectedly found that even a low-dose CBD regimen led to clinically meaningful liver enzyme elevations in 5.6%
The biosimilar demonstrated comparable efficacy and safety to Stelara in a phase 3 clinical trial, supporting its FDA approval. Steqeyma provides a new dosage form and strength, enhancing treatment flexibility for young patients with chronic inflammatory conditions.
Subcutaneous injection Oral tablet What is the standard dosage? If needed, the dosage may be increased to 5 mg once weekly. The dosage can then be increased by 2.5 Adults Adults and children 10 and older Mounjaro and Farxiga are approved by the Food and Drug Administration (FDA) to manage Type 2 diabetes mellitus.
2,3 LIMBER is a phase 1, open-label, dose escalation study evaluating INCB057643 as a monotherapy at a dose escalation of 4 to 12 mg daily (part 1) or in combination with ruxolitinib at a dosage of 4 mg once daily and escalating to the maximum tolerated dose in part 1 (part 2).
As a prescription opioid, it has different approved uses based on the dosage form: Injectable fentanyl is used as a pain reliever during or after surgery or as an add-on to general or local anesthesia. Fentanyl may also be prescribed off-label, meaning for a purpose other than what the Food and Drug Administration (FDA) approved it for.
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Rumore, PharmD, Esq, MS, LLM, FAPhA Key Takeaways The removal of tirzepatide and semaglutide from the FDA's shortage list impacts 503A compounders, requiring adherence to complex legal and regulatory frameworks. SHOW MORE GLP-1 compounding faces legal challenges, evolving FDA rules, and heightened enforcement risks.
Some options include : Repatha (evolocumab) is a brand-name medication that is FDA approved to lower cholesterol and reduce the risk of heart attacks and strokes, by helping to restore blood flow to the heart in individuals with heart disease. Taking a lower dosage may help to lower your risk of side effects from statins.
Jardiance (empagliflozin) is a brand-name prescription drug that has been FDA approved as a supplement to diet and exercise to improve blood sugar levels in people with Type 2 diabetes. Take Jardiance as directed Jardiance dosage for blood sugar control ranges from 1025 mg daily. Its important to take the dosage as prescribed.
This combination allows your heart to pump blood more efficiently, managing certain types of heart failure in adults and children older than 1, and helping to lower the risk of death and hospitalization. While Entresto is not FDA approved in the U.S. Decreased blood pressure is a side effect of Entresto.
Both agents received FDA approval for the treatment of patients with RRMM who have received at least 4 prior lines of therapy, including a proteasome inhibitor, an immunomodulatory agent, and an anti-CD38 antibody. The investigators assessed a total of 90 patients who received talquetamab at a dosage of 0.8 mg/kg every 2 weeks.
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