The MPR Drug Reference Database for Healthcare Practitioners

You can browse drugs by brand, generic, therapeutic category, or manufacturer. Also, you can view new drug products and monograph updates , as …

Actived: 5 days ago

URL: Empr.com

Prescription & OTC Drug Info Side Effects, Interactions & Dosages

(1 days ago) MPR provides drug monographs, drug news and e-prescribing service for healthcare professionals. We provides drug dosing, interactions, recalls and more for medical professionals.

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Prescription & OTC Drug Info Side Effects, Interactions & Dosages

(6 days ago) Drugs in the Pipeline. CAR-T Cell Therapy Fast Tracked for B-Cell Non-Hodgkin’s Lymphoma By Steve Duffy. Publish Date April 19, 2022 A phase 1 trial is currently evaluating the safety and

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Browse by Drug Brands

(5 days ago) Court Rules That State’s Medical Malpractice Act Can Apply to Nonpatients; Interview With Dr Tobias Janowitz on Conducting Fully Remote Trials

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April 2022: Drug Pipeline Updates

(5 days ago) Brian Park, PharmD. The table provided is a review of notable updates that occurred in April 2022 for investigational products in development. Treatment of eosinphilic esophagitis in patients 12

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Confused Drug Names

(2 days ago) Confused Drug Names according to ISMP guidelines. Court Rules That State’s Medical Malpractice Act Can Apply to Nonpatients

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Antiemetic Treatments

(4 days ago) A list of drugs used for the treatment of nausea. The chart includes the formulations, strengths, and usual doses for each antiemetic drug product.

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Sparsentan Gets Priority Review for IgA Nephropathy

(5 days ago) The Food and Drug Administration (FDA) has accepted for Priority Review the New Drug Application for sparsentan for the treatment of immunoglobulin A (IgA) nephropathy. IgA nephropathy (IgAN) is a

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NDA Submitted for Continuous SC Infusion Therapy for Parkinson …

(4 days ago) ABBV-951 is a solution of levodopa and carbidopa prodrugs for continuous subcutaneous infusion.

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Gabapentin-Involved Overdose Deaths Increased Between 2019 …

(9 days ago) When assessing quarterly trends, the data showed an increase in gabapentin-involved deaths, from 49.4% in the first quarter of 2019 to 55.1% during the …

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Nyxol Ophthalmic Solution Looks Promising for Night Vision …

(5 days ago) Nyxol is a once-daily, preservative-free eye drop formulation of phentolamine mesylate, a nonselective alpha-1 and alpha-2 adrenergic antagonist …

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Predicting Lung Cancer: Risk-Based LDCT Screening vs Age and …

(Just Now) Credit: Getty Images . Screening via risk-based low-dose computed tomography (LDCT) is a better predictor of lung cancer risk than age and pack years. Early involvement of …

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February 2022: 5 Notable Drug Approvals

(8 days ago) Notable FDA drug approvals for February 2022 include Carvykti, Enjaymo, Nalmefene HCl Injection, Pyrukynd, and Vonjo.

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Annovera Product Supply Expected to Increase Following FDA …

(9 days ago) The Food and Drug Administration (FDA) has approved the supplemental New Drug Application (sNDA) for Annovera® (segesterone acetate and ethinyl …

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Which Biologics Reduce Allergic Response, Airway …

(9 days ago) Credit: Getty Images . Among patients with asthma, early and late allergic responses were reduced with omalizumab and tezepelumab, according to systematic review findings presented at …

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FDA Modifies REMS Requirements for Opioid Analgesic Dsuvia

(Just Now) The Risk Evaluation and Mitigation Strategies (REMS) requirements for Dsuvia® (sufentanil) have recently been modified by the Food and Drug Administration (FDA) with regard to …

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FDA Approves IV Formulation of Tpoxx for Smallpox

(1 days ago) Credit: Getty Images . The Food and Drug Administration (FDA) has approved the intravenous (IV) formulation of Tpoxx ® (tecovirimat) for the treatment of human smallpox disease caused by …

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Trial Evaluating Pemafibrate to Reduce CV Outcomes in Diabetes …

(8 days ago) Credit: . A phase 3 study evaluating pemafibrate (K-877) to reduce cardiovascular outcomes in high-risk adults with type 2 diabetes has been discontinued. Pemafibrate is an investigational

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Dasiglucagon Reduces Glucose Requirements in Congenital …

(1 days ago) The clinical trial (ClinicalTrials.gov Identifier: NCT04172441) evaluated the efficacy and safety of dasiglucagon administered as a continuous intravenous (IV) infusion via a pump in 12 children

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Tasquinimod Gets Orphan Drug Designation for Myelofibrosis

(2 days ago) The Food and Drug Administration (FDA) has granted Orphan Drug designation to tasquinimod for the treatment of myelofibrosis. Tasquinimod is …

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Does Pulmonary Rehabilitation Improve Outcomes of Post-COVID …

(1 days ago) Pulmonary rehabilitation has been suggested to address post-COVID sequelae affecting exercise capacity, quality of life, and productivity up to 6 months after the initial disease. Credit: Getty

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FDA Decision on Bimekizumab for Plaque Psoriasis Delayed

(Just Now) Credit: Getty Images . The Food and Drug Administration (FDA) has issued a Complete Response Letter (CRL) to UCB regarding the Biologics License Application (BLA) for bimekizumab for the treatment

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Oral Treatment for COVID-19 Gains Fast Track Designation

(Just Now) Credit: Getty Images . The Food and Drug Administration (FDA) has granted Fast Track designation to EPD-235, an investigational antiviral for the treatment and prevention of …

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CDC: Be Alert for Rashes Consistent With Monkeypox

(1 days ago) State health departments and the CDC’s Emergency Operations Center should be consulted on any suspected cases of monkeypox. The CDC is currently investigating 1 case of …

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Opdualag Approved for Unresectable, Metastatic Melanoma

(6 days ago) The Food and Drug Administration (FDA) has approved Opdualag (nivolumab and relatlimab-rmbw) for the treatment of patients 12 years of age and …

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Inhaled Therapy Gets Breakthrough Designation for Non-Cystic …

(8 days ago) The Food and Drug Administration (FDA) has granted Breakthrough Therapy designation to colistimethate sodium powder for nebulization solution (CMS I–neb ®) …

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Sabizabulin Cuts COVID-19 Death; Trial Stopped Early Due to …

(1 days ago) The phase 3 trial included approximately 210 patients hospitalized with moderate to severe COVID-19 (WHO ≥4) who were at high risk for ARDS and death.

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FDA to Review Wearable Furosemide Delivery System for …

(2 days ago) The Food and Drug Administration (FDA) has accepted for filing the New Drug Application (NDA) for Furoscix ® for the treatment of congestion due to …

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FDA Says No to Vadadustat Approval Due to Safety Concerns

(1 days ago) Vadadustat is an oral hypoxia-inducible factor prolyl hydroxylase inhibitor designed to mimic the physiologic effect of altitude on oxygen availability. This results in increased red blood cell

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Significant Improvements in Myasthenia Gravis Seen With …

(6 days ago) Significant improvements for all endpoints were observed as early as week 1. Moreover, a significantly greater proportion of patients in the zilucoplan arm …

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March 2022: Drug Pipeline Updates

(6 days ago) The table below is a review of notable pipeline updates that occurred in March 2022 for investigational products in development (not an inclusive list). …

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Elamipretide Gets Orphan Drug Status for Friedreich Ataxia

(2 days ago) The Food and Drug Administration has granted Orphan Drug designation to elamipretide for the treatment of Friedreich ataxia. Friedreich ataxia is a rare …

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The Antidepressants Most Commonly Abused, Misused

(Just Now) the MPR take: Although the majority of patients on antidepressant therapy are not taking the drugs for nonmedical use or abusing them, there is a potential for misuse; this is particularly

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Lilly Ends Baricitinib Lupus Program, Provides Update on Atopic

(2 days ago) Baricitinib is a Janus kinase inhibitor. Credit: Lilly. Lilly has decided to discontinue the phase 3 development program for baricitinib in adults with active systemic lupus erythematosus. The

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FDA Accepts Resubmitted Eflapegrastim BLA for Chemotherapy …

(2 days ago) The Food and Drug Administration (FDA) has accepted for filing the resubmitted Biologics License Application (BLA) for eflapegrastim to decrease the incidence of infection, as manifested by

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Oral Antiviral Treatments for COVID-19: Molnupiravir and Paxlovid

(6 days ago) Initiate as soon as possible after diagnosis of COVID-19 and within 5 days of symptom onset. Prescriptions should specify the numeric dose of each …

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Efgartigimod Looks Promising for Primary Immune …

(8 days ago) A clinically meaningful improvement in platelet count was observed in a significantly higher proportion of patients with chronic primary immune thrombocytopenia (ITP) …

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